Five abstracts accepted for poster presentations
2025 (GLOBE NEWSWIRE) -- Arbutus Biopharma Corporation (Nasdaq: ABUS) (“Arbutus” or the “Company”)
a clinical-stage biopharmaceutical company focused on infectious disease
have been accepted for presentation at the European Association for the Study of the Liver (EASL) Congress 2025 taking place May 7 - 10
The following abstracts will be presented as posters in the Viral Hepatitis B and D: New Therapies
Unapproved Therapies or Strategies session on May 8
Abstract Number: 1768Title: IM-PROVE I: characterization of chronic hepatitis B (CHB) subjects with functional cure or HBV DNA suppression after completion of imdusiran plus short courses of pegylated interferon alfa-2a (IFN) and discontinuation of nucleos(t)ide analogue (NA) therapyPresenter: Prof
2025Key Findings: Within this small group of subjects who achieved functional cure or HBV DNA<LLOQ after NA discontinuation in the IM-PROVE I study
HBsAg at baseline and at the time of NA discontinuation appear to be the only factors associated with functional cure
with no apparent differences in other baseline characteristics or HBV biomarkers collected
Additional analysis of this dataset is ongoing
and the potential association of baseline characteristics and HBV biomarkers with functional cure should continue to be evaluated in larger trials
This will also be featured in the Poster Tour: Viral Hepatitis
Abstract Number: 2043Title: IM-PROVE I: Rapid loss followed by transient increases in HBV RNA in chronic hepatitis Bsubjects during treatment with imdusiran and pegylated interferon alfa-2a is associated with HBsAg seroclearancePresenter: Dr
2025Key Findings: Subjects who achieved functional cure after combination treatment with imdusiran plus interferon showed rapid HBV RNA decline during imdusiran lead-in
with 5 of 6 subjects achieving HBV RNA undetectability during this period
Transient elevations in HBV RNA were observed to occur during the interferon treatment period which was associated with further HBsAg decline and loss in some functional cure subjects
Abstract Number: 1990Title: First-in-human pharmacokinetics and pharmacodynamics of oral small-moleculePD-L1 inhibitor AB-101 and correlation to preclinical modelsPresenter: Dr
2025Key Findings: AB-101 was safe and well-tolerated in both single- and multiple-dose administrations in healthy subjects
Dose-responsive increases in PD-L1 receptor occupancy were observed in peripheral blood cells
which correlated with dose-dependent increases in AB-101 plasma concentrations
The clinical plasma PK profile of AB-101 to date indicates rapid distribution into tissues
mirroring the plasma profiles seen in preclinical efficacy models
which exhibited high liver biodistribution and target engagement
Abstract Number: 1978Title: Preliminary safety
pharmacokinetics and pharmacodynamics of single and multiple doses of AB-101
in healthy and chronic hepatitis B subjectsPresenter: Prof
2025Key Findings: Single doses of AB-101 up to 40 mg and repeat doses up to 40 mg QD for 7 days were well tolerated in healthy subjects
Preliminary PD data shows AB-101 receptor occupancy at doses ≥ 10 mg
with dose-responsive increases in PD-L1 receptor occupancy observed
Dosing in Part 3 in CHB subjects is ongoing and available data
including receptor occupancy and HBV virologic biomarkers
The following late-breaker poster will be presented on May 7
Abstract Number: LB25153Title: Off-treatment antiviral efficacy and safety of repeat dosing of imdusiran followed by VTP-300 with or without nivolumab in virally-suppressed
non-cirrhotic subjects with chronic hepatitis B (CHB)Presenter: Dr
Imdusiran is an RNAi therapeutic specifically designed to reduce all HBV viral proteins and antigens including hepatitis B surface antigen
which is thought to be a key prerequisite to enable reawakening of a patient’s immune system to respond to the virus
Imdusiran targets hepatocytes using Arbutus’ novel covalently conjugated N-Acetylgalactosamine (GalNAc) delivery technology enabling subcutaneous delivery
imdusiran achieved meaningful functional cure rates in patients with cHBV when combined with pegylated interferon (IFN) alfa-2α and nucleos(t)ide analogue (NA) therapy
Clinical data generated thus far has shown imdusiran to be generally safe and well-tolerated
while also providing meaningful reductions in hepatitis B surface antigen and hepatitis B DNA
The Company is currently reviewing development plans for a Phase 2b clinical trial of imdusiran combined with IFN and NA therapy
AB-101 is an oral PD-L1 inhibitor candidate that is designed to allow for controlled immune checkpoint blockade while minimizing the systemic safety issues typically seen with immune checkpoint antibody therapies
Immune checkpoints such as PD-1/PD-L1 play an important role in the induction and maintenance of immune tolerance and in T-cell activation
Preclinical data generated thus far indicates that AB-101 mediates re-activation of exhausted HBV-specific T-cells from cHBV patients
AB-101 is currently being evaluated in a Phase 1a/1b clinical trial
Hepatitis B is a potentially life-threatening liver infection caused by the hepatitis B virus (HBV)
HBV can cause chronic infection which leads to a higher risk of death from cirrhosis and liver cancer
Chronic HBV infection represents a significant unmet medical need
The World Health Organization estimates that over 250 million people worldwide suffer from chronic HBV infection
while other estimates indicate that approximately 2 million people in the United States suffer from chronic HBV infection
Approximately 1.1 million people die every year from complications related to chronic HBV infection despite the availability of effective vaccines and current treatment options
Forward-Looking Statements and Information
This press release contains forward-looking statements within the meaning of the Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934
and forward-looking information within the meaning of Canadian securities laws (collectively
Forward-looking statements in this press release include statements about: the potential to lead to a functional cure for HBV; the result of Arbutus’ review of its pipeline and development plans for its cHBV programs and the potential for Arbutus’ product candidates to achieve success in clinical trials
With respect to the forward-looking statements contained in this press release
Arbutus has made numerous assumptions regarding
among other things: the effectiveness and timeliness of clinical trials
and the usefulness of the data; the timeliness of regulatory approvals; the continued demand for Arbutus’ assets; and the stability of economic and market conditions
While Arbutus considers these assumptions to be reasonable
these assumptions are inherently subject to significant business
market and social uncertainties and contingencies
there are known and unknown risk factors which could cause Arbutus’ actual results
performance or achievements to be materially different from any future results
performance or achievements expressed or implied by the forward-looking statements contained herein
among others: ongoing and anticipated clinical trials may be more costly or take longer to complete than anticipated
or may not generate results that warrant future development of the tested product candidate; Arbutus may elect to change its strategy regarding its product candidates and clinical development activities; Arbutus may not receive the necessary regulatory approvals for the clinical development of Arbutus’ products; economic and market conditions may worsen; and market shifts may require a change in strategic focus
All forward-looking statements herein are qualified in their entirety by this cautionary statement
and Arbutus disclaims any obligation to revise or update any such forward-looking statements or to publicly announce the result of any revisions to any of the forward-looking statements contained herein to reflect future results
Officials identified the officer who fatally shot a man in Arbutus on Wednesday as a 28-year veteran of the Baltimore County Police Department
Detective Todd Weidel is the officer who fatally shot Arvel Jones Sr., 51, in Arbutus after reports that he was shooting arrows at passing cars, the Maryland attorney general’s office announced
Investigators said Jones donned a black ski mask
wielded a bow-and-arrow and fired it at passing cars on Wednesday
Weidel and another officer separately responded to a call about Jones’ actions around 10:30 a.m
Weidel was not equipped with a body-worn camera
The other officer did not activate his body-worn camera until after the incident
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Officials said Weidel and the other officer
provided aid until EMS arrived to bring Jones to the hospital
Weidel has been with the Baltimore County Police Department for 28 years
according to the attorney general’s office
Jones’ son, Arvel Jones Jr., told WJZ-TV his father was likely having a mental health episode
but that he was a nonviolent man who “wouldn’t hurt a fly.”
but that doesn’t make it right for you to take his life,” Arvel Jones Jr
Jones’ shooting rattled the small Arbutus community
where movement and classes continued as the outside was secured
Neighbors sat in shock at the incident happening so close to their home
WJZ is a media partner of The Baltimore Banner
Darreonna Davis
darreonna.davis@thebaltimorebanner.com
Darreonna Davis is an express desk reporter at The Baltimore Banner
She previously reported at the intersection of gender
health and economic policy as a fellow for the 19th News
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— We're learning more of what led to a deadly police involved shooting in Arbutus Wednesday
According to the Maryland Attorney General's Office
officers were called to the 5100 block of Leeds Avenue for reports of a masked man shooting at passing cars with a bow and arrow
When Baltimore County Police arrived on scene around 10:30am
they encountered a suspect meeting the description provided by the 911 caller
While it's unclear what transpired from there
RELATED: Man reportedly armed with bow and arrow shot and killed by police in Arbutus
The Attorney General's Independent Investigative Division is handling the deadly force aspect of the case
meaning portions of the incident were captured on video
which could be released sometime in the next couple weeks
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but her spirit will live on in the hearts of all who knew and loved her
her personality radiating warmth that embraced everyone around her
Her humor was a gift that she shared generously; it brought joy to gatherings and laughter to conversations
ultimately creating a legacy of care and compassion that will be felt for generations
She shared profound bonds with her children
and reveled in the love of her cherished grandson
Arbutus’s life was enriched by her deep connection to her siblings: Nellie Russo Foisy of Lorain
and created memories that will forever echo in their hearts
Arbutus found joy in crocheting intricate patterns
often sharing those hours with her beloved great nieces
infusing her family gatherings with delicious aromas and flavorful dishes that left lasting impressions
Arbutus could often be found singing her favorite songs
her voice bringing warmth and familiarity to those who listened
They will undoubtedly welcome her with open arms
as she brings her characteristic humor and loving spirit to the heavens
Arbutus Russo Comstock’s impact on this world cannot be measured; she was a true embodiment of love
Her memory will continue to shine brightly through the stories shared and the love passed down through the generations she touched
Though she has departed from this earthly realm
her spirit will forever remain a guiding force for all those who cherished her
Funeral arrangements entrusted to Slone & Co
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iStock, Andry Djumantara
Arbutus Biopharma is letting go of 57% of its staff
bringing the Pennsylvania biotech down to a “core team” of 19 employees who will focus on its hepatitis B program
according to a press announcement on Thursday
Arbutus is also terminating all in-house scientific research and will leave its corporate headquarters in Warminster
the biotech expects to absorb one-time costs of around $11 million to $13 million in the first quarter
Arbutus is also thinning out its masthead: chief financial officer David Hastings
chief medical officer Karen Sims and chief compliance officer Christopher Naftzger will all be stepping down from their leadership roles
It is unclear how much Arbutus expects to save from these strategic moves but CEO Lindsay Androski noted in a statement on Thursday that they will help “improve our financial and operational efficiency.”
Arbutus on Thursday named Tuan Nguyen as its new CFO
whose appointment “reinforces our renewed focus on advancing our pipeline efficiently and delivering value to patients and our stakeholders,” Androski said
Arbutus is “reviewing development plans” for pushing imdusiran into Phase IIb
including looking for ways to potentially accelerate its timeline
Arbutus is also working on an oral PD-L1 blocker
which it is developing for chronic hepatitis B
The asset is currently in a Phase Ia/Ib trial that is mostly assessing its safety and tolerability
The biotech has moved forward with the third part of this early study
It has yet to disclose next steps for the asset
cash equivalents and marketable securities
down from a cash position of $132.3 million the year prior
the biotech “expects to significantly reduce its net cash burn” this year
though it did not provide guidance on how long it expects its runway to last
2025 at 12:50 pm ET.css-79elbk{position:relative;}Authorities have released the name of a man armed with a bow and arrow who was fatally shot Wednesday by Baltimore County police
along with the name of the officer who fired the shot
MD — The name of a man armed with a bow and arrow who was fatally shot Wednesday in Arbutus by Baltimore County police — sparking brief lockouts at three nearby schools — was released Friday by officials
of Arbutus died at an area hospital after he was confronted by police officers in the 5100 block of Leeds Avenue around 10:25 a.m
The Independent Investigations Division of the Maryland Office of the Attorney General released the name of Jones and the officer who fired at him
The Baltimore County Police Department said Detective Todd Wiedel
a 28-year veteran of the department assigned to the Operations Bureau
"During this encounter, officers responded to the actions of the armed subject, resulting in one detective discharging his firearm, striking the adult male," the Baltimore County Police Department said in a press release
Officers said they immediately administered life-saving measures to Jones
Arbutus Middle School and Maiden Choice School were briefly put on lockout status
Arbutus Elementary Principal Samantha Maile said the lockout started around 10:30 a.m
after "our Safety Manager made us aware of an individual in the community who was shooting a crossbow," and ended within 10 minutes
no one can enter or leave the building without the principal’s permission
Entry to or exit from a building is granted on a case-by-case basis and usually in conjunction with the Baltimore County Police Department," Maile wrote in a letter to families
The IID continues to investigate the fatal officer-involved shooting. Anyone with information about this incident, including cell phone or private surveillance video, is asked to contact the IID at (410) 576-7070 or by email at IID@oag.state.md.us.
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We are learning more about the man shot and killed by police in Baltimore County.
The Independent Investigations Division says the officer who fatally shot a man armed with a bow and arrow in Arbutus on Wednesday was not equipped with a body-worn camera
Police responded to the 5100 block of Leeds Avenue after neighbors reported a man wearing a ski mask and carrying a bow and arrow
Two officers were dispatched to the scene and approached the suspect
According to the Maryland Attorney General’s Office
the man’s actions prompted one of the officers to open fire
Officials confirmed that the officer who fired the fatal shot was not wearing a body camera
and the other officer’s camera was not activated until after the incident
The man was later pronounced dead at the hospital
The Independent Investigations Division is asking anyone with video footage of the incident to contact their office
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Claim construction hearing for Pfizer/BioNTech mRNA-LNP vaccine litigation occurred in December 2024; outcome pending
mRNA-LNP vaccine litigation scheduled for September 2025
Reviewing pipeline and development plans for HBV programs
Continued focus on efficient deployment of financial resources and personnel – terminated ATM program and implemented reduction of workforce by 57% in Q1 2025
Board has approved further changes to executive leadership team; including the appointment of Tuan Nguyen as Chief Financial Officer
cash equivalents and investments in marketable securities of $123M
today reported fourth quarter and year end 2024 financial results and provided a corporate update
“With my recent appointment as CEO of Arbutus
I am excited to lead the company into its next chapter,” said Lindsay Androski
my focus is on evaluating strategies to accelerate the development and potential approval of imdusiran
alongside several subject matter experts being retained to assist with this evaluation
we have implemented a reduction in our workforce of 57%
retaining a core team well-positioned to advance imdusiran into a Phase 2b trial
and have taken additional related steps to improve our financial and operational efficiency
We will provide an update on our pipeline and development timeline upon completion of our review of our chronic hepatitis B virus (cHBV) programs.”
“I am also excited to welcome Tuan Nguyen to our leadership team as Chief Financial Officer
Tuan’s appointment reinforces our renewed focus on advancing our pipeline efficiently and delivering value to patients and our stakeholders
the Company announced today the departure of David Hastings
and I would like to thank them for their valuable contributions over the past years
We will continue to consult closely with and support our exclusive licensee Genevant Sciences to protect and defend our intellectual property
including through recently filed international lawsuits against Moderna for patent infringement in the development of its COVID-19 and RSV vaccines
We expect 2025 to be a transformative year for Arbutus.”
cash equivalents and investments in marketable securities of $122.6 million compared to $132.3 million as of December 31
the Company used $64.9 million in operating activities
which was partially offset by $44.1 million of net proceeds from the issuance of common shares under its “at-the-market” (ATM) offering program and $7.5 million of proceeds from the exercise of employee stock options
The Company expects to significantly reduce its net cash burn in 2025 when compared to 2024
Given the Company’s review of its pipeline and development plans for its cHBV programs and refocused operations
the Company has terminated its ATM offering program
Total revenue was $6.2 million for the year ended December 31
compared to $18.1 million for the same period in 2023
The decrease of $11.9 million was due primarily to a $9.3 million decrease in revenue recognition of the upfront license fee received in 2022 from Qilu
the Company’s collaboration partner in China
as less effort was required from the Company in 2024 compared to 2023 to support Qilu’s progress towards achieving its own imdusiran manufacturing capability
license royalty revenues decreased $2.6 million in 2024 compared to 2023 due to a decrease in Alnylam’s sales of ONPATTRO
Research and development expenses were $54.0 million for the year ended December 31
2024 compared to $73.7 million for the same period in 2023
which included ceasing all discovery efforts
discontinuing its IM-PROVE III clinical trial and reducing its workforce by 40%
These actions in August 2024 resulted in the Company incurring a one-time restructuring charge of $3.7 million in the third quarter of 2024
General and administrative expenses were $22.1 million for the year ended December 31
compared to $22.5 million for the same period in 2023
This decrease was due primarily to decreases in employee compensation-related expenses
partially offset by an increase in litigation-related legal fees
or a loss of $0.38 per basic and diluted common share
as compared to a net loss of $72.8 million
or a loss of $0.44 per basic and diluted common share
the Company had 190.0 million common shares issued and outstanding
as well as 16.9 million stock options and unvested restricted stock units outstanding
owned approximately 20% of the Company’s outstanding common shares as of December 31
The Company is currently reevaluating plans for a Phase 2b clinical trial of imdusiran combined with IFN and NA therapy
AB-101 is an oral PD-L1 inhibitor candidate that is designed to allow for controlled checkpoint blockade while minimizing the systemic safety issues typically seen with checkpoint antibody therapies
Forward-looking statements in this press release include statements about: the potential to lead to a functional cure for HBV; the result of Arbutus’ review of its pipeline and development plans for its cHBV programs; the potential for Arbutus’ product candidates to achieve success in clinical trials; Arbutus’ plans with respect to the ongoing patent litigation matters
and the expected timing thereof; the potential that the management changes will renew focus on advancing the Company’s pipeline efficiently and delivering value to patients and Arbutus’ stakeholders; the expectation that 2025 will be a transformative year for Arbutus; and Arbutus’ expected financial condition
or investor perceptions; and risks related to the sufficiency of Arbutus’ cash resources for its foreseeable and unforeseeable operating expenses and capital expenditures
2025 at 6:42 pm ET.css-79elbk{position:relative;}The Baltimore County Police Department said it fatally shot a man armed with a bow and arrow Wednesday in Arbutus
(Jacob Baumgart/Patch Stock Photo)Last updated Wednesday at 6:42 p.m
MD — Police said they fatally shot a man armed with a bow and arrow Wednesday in Arbutus
sparking brief lockouts at three nearby schools
Officers said they were called to the 5100 block of Leeds Avenue around 10:25 a.m
Authorities said police in uniform and plain clothes engaged the armed man
"During this encounter, officers responded to the actions of the armed subject, resulting in one detective discharging his firearm striking the adult male," the Baltimore County Police Department said in a press release
Officers said they immediately administered life-saving measures
Authorities said the man was taken to a nearby hospital
Police announced at 10:47 a.m. on X
that "residents can expect a police presence in the area" of Leeds Avenue and Greystone Road
Arbutus Middle School and Maiden Choice School were put on lockout status
after "our Safety Manager made us aware of an individual in the community who was shooting a crossbow." The lockout was lifted at 10:38 a.m
Maryland Attorney General Anthony Brown at 1:24 p.m. confirmed the fatality
Brown's office is legally required to investigate all deadly encounters with police
"I want you to be assured that the safety of our students is our top priority
please do not hesitate to contact the school," Maile said
2025 (GLOBE NEWSWIRE) -- Genevant Sciences
a leading nucleic acid delivery company with world-class platforms and a robust lipid nanoparticle (LNP) patent portfolio (a subsidiary of Roivant Sciences
and Arbutus Biopharma Corporation (Nasdaq: ABUS)
today filed five international lawsuits seeking to enforce patents protecting their innovative LNP technology against Moderna
the enforcement actions target alleged infringing activities in 30 countries
Genevant and Arbutus are seeking monetary relief and injunctions against Spikevax® and
additional Moderna products that Moderna has represented use the same LNP technology
Genevant and Arbutus submitted evidence from testing of commercial Moderna product samples sourced from the U.S
and Europe indicating that the samples contain LNPs falling under the protective scope of the claims of their lipid composition patents
The UPC actions together seek relief for: Austria
Today’s actions expand on Arbutus and Genevant’s ongoing enforcement proceeding in the U.S
District Court for the District of Delaware
seeking fair compensation for Moderna’s alleged infringement of six U.S
patents in the manufacture and sale of Spikevax®
A jury trial is currently scheduled for September 2025
It is well established in the scientific literature that the most significant technological hurdle to developing and deploying medicines using mRNA is engineering a safe and effective way to deliver the mRNA to human cells
Scientists at Arbutus and Genevant have spent years developing and refining LNP delivery technology
which has been licensed for various applications to many different third parties
Arbutus and Genevant’s LNP technology relies on microscopic particles built from four carefully selected types of fat-like molecules to shelter and protect mRNA molecules and to enable them to travel through the human body to a target cell and through the target cell’s membrane before releasing the mRNA
mRNA would quickly degrade in the body and be ineffective
Forward-looking statements in this press release include
statements about: Arbutus’ plans with respect to the ongoing patent litigation matters
Arbutus disclaims any obligation to revise or update any such forward-looking statements or to publicly announce the result of any revisions to any of the forward-looking statements contained herein to reflect future results
Left to cherish her memory are her parents
Roger Cannady and Daisy Arbutus Cannady of Vander
her beloved husband Joseph Link of the home
(Kaitlynn) of Lumberton and Jeremiah Link (Morgan) of Bladenboro
Loretta Ketterman (Jack) of Vander and one grandson
Daisy was a devoted and loving daughter
She enjoyed spending time with them whether it was fishing
trips to the beach or mountains or sitting down to a meal together
Daisy loved nothing better than spoiling her grandson Jacob and baking goodies for the family
Her unconditional love is the legacy that will forever hold their hearts
A 16-year-old boy was fatally shot in a residential neighborhood in Arbutus on Sunday afternoon
Officers were dispatched to the 4000 block of Alan Drive off Wilkens Avenue for reports of shots fired around 2:10 p.m
they found a teenage victim who had sustained at least one gunshot wound
The victim was later pronounced dead on the scene
They request anyone with information about the case to contact 410-887-4636 (INFO)
Sapna Bansil
sapna.bansil@thebaltimorebanner.com
Sapna Bansil is a regional reporter and Roy W
She graduated in May 2024 with her master's from the University of Maryland and held internships at The Philadelphia Inquirer and The Washington Post
2025 (GLOBE NEWSWIRE) -- Arbutus Biopharma Corporation (Nasdaq: ABUS) (“Arbutus” or the “Company”)
today announced changes to its board of directors and the appointment of Lindsay Androski
Androski will also serve as a member of the Company’s board of directors
Androski is an MIT-trained biologist with nearly 30 years of experience in the areas of biotechnology
She has served in a variety of roles at Roivant
She is currently special counsel at Genevant with responsibilities including LNP litigation
“I would like to thank Michael McElhaugh and the rest of the board for their service,” said Lindsay Androski
I am excited to lead the company into its next chapter
We believe these changes in leadership will enable renewed focus on advancing the company’s pipeline efficiently and maximizing the company’s contributions to LNP delivery technology through Genevant
both of which we expect will deliver greater value to shareholders and patients alike.”
four new directors have joined the board: Robert Alan Beardsley
In connection with the appointment of these new directors
all members of the existing board of directors have stepped down effective immediately and the board was reduced to five members in total
The Company is considering additional directors with expertise in clinical development and may expand the board in the coming months
The Company will temporarily pause participation in investor meetings and conferences while the new board and management team reviews development plans and strategic options for its hepatitis B programs
statements about Arbutus’s consideration of additional directors for its board
Genevant Sciences and Arbutus Biopharma (ABUS) have initiated five international patent infringement lawsuits against Moderna across 30 countries
The legal actions target Moderna's alleged unauthorized use of their lipid nanoparticle (LNP) technology in Spikevax® and mRESVIA® products
The lawsuits have been filed in multiple jurisdictions including Canada
The companies are seeking monetary damages and injunctions against Moderna's products
Evidence from testing commercial Moderna samples from the U.S
and Europe indicates the presence of LNPs that fall under their patent claims
This international enforcement expands on their ongoing U.S
where a jury trial is scheduled for September 2025
was developed by Arbutus and Genevant scientists and has been licensed to various third parties
Genevant Sciences e Arbutus Biopharma (ABUS) hanno avviato cinque cause legali internazionali per violazione di brevetto contro Moderna in 30 paesi
Le azioni legali mirano all'uso presunto non autorizzato della loro tecnologia dei nanoparticelle lipidiche (LNP) nei prodotti Spikevax® e mRESVIA®
Le cause sono state depositate in diverse giurisdizioni
Svizzera e il Tribunale Unificato dei Brevetti (UPC)
Le aziende stanno cercando risarcimenti monetari e ingiunzioni contro i prodotti di Moderna
Le prove ottenute testando campioni commerciali di Moderna provenienti da Stati Uniti ed Europa indicano la presenza di LNP che rientrano nelle loro rivendicazioni di brevetto
Questa enforcement internazionale si aggiunge al procedimento in corso negli Stati Uniti in Delaware
dove è previsto un processo con giuria per settembre 2025
importante per la somministrazione di medicinali mRNA
è stata sviluppata da scienziati di Arbutus e Genevant ed è stata concessa in licenza a vari terzi
Genevant Sciences y Arbutus Biopharma (ABUS) han iniciado cinco demandas internacionales por infracción de patentes contra Moderna en 30 países
Las acciones legales se dirigen al supuesto uso no autorizado de su tecnología de nanopartículas lipídicas (LNP) en los productos Spikevax® y mRESVIA®
Las demandas se han presentado en múltiples jurisdicciones
Suiza y el Tribunal de Patentes Unificado (UPC)
Las empresas buscan daños monetarios e interdictos contra los productos de Moderna
La evidencia de pruebas de muestras comerciales de Moderna de EE
y Europa indica la presencia de LNP que se encuentran bajo sus reclamaciones de patente
Esta aplicación internacional se suma al procedimiento en curso en EE
donde se programó un juicio con jurado para septiembre de 2025
importante para la entrega de medicamentos de ARNm
fue desarrollada por científicos de Arbutus y Genevant y ha sido licenciada a varios terceros
Genevant Sciences와 Arbutus Biopharma (ABUS)는 Moderna에 대해 30개국에서 다섯 건의 국제 특허 침해 소송을 시작했습니다
이 법적 조치는 Spikevax® 및 mRESVIA® 제품에서 그들의 지질 나노입자(LNP) 기술의 무단 사용을 겨냥하고 있습니다
이들 회사는 Moderna의 제품에 대한 금전적 손해배상과 금지 명령을 요청하고 있습니다
mRNA 의약품 전달에 중요한 LNP 기술은 Arbutus와 Genevant 과학자들에 의해 개발되었으며 여러 제3자에게 라이선스가 부여되었습니다
Genevant Sciences et Arbutus Biopharma (ABUS) ont engagé cinq poursuites internationales pour violation de brevet contre Moderna dans 30 pays
Les actions en justice visent l'utilisation présumée non autorisée de leur technologie des nanoparticules lipidiques (LNP) dans les produits Spikevax® et mRESVIA®
Les poursuites ont été déposées dans plusieurs juridictions
la Suisse et le Tribunal Unifié des Brevets (UPC)
Les entreprises demandent des dommages-intérêts et des injonctions contre les produits de Moderna
Des preuves provenant de tests d'échantillons commerciaux de Moderna des États-Unis et d'Europe indiquent la présence de LNP qui relèvent de leurs revendications de brevet
Cette application internationale s'ajoute à la procédure en cours aux États-Unis dans le Delaware
où un procès avec jury est prévu pour septembre 2025
importante pour la délivrance de médicaments à ARNm
a été développée par des scientifiques d'Arbutus et de Genevant et a été concédée sous licence à divers tiers
Genevant Sciences und Arbutus Biopharma (ABUS) haben fünf internationale Klagen wegen Patentverletzung gegen Moderna in 30 Ländern eingereicht
Die rechtlichen Schritte zielen auf die angebliche unbefugte Nutzung ihrer Lipid-Nanopartikel (LNP)-Technologie in den Produkten Spikevax® und mRESVIA® ab
Die Klagen wurden in mehreren Jurisdiktionen eingereicht
die Schweiz und das Einheitliche Patentgericht (UPC)
Die Unternehmen fordern finanzielle Entschädigungen und Unterlassungsverfügungen gegen die Produkte von Moderna
Beweise aus Tests kommerzieller Moderna-Proben aus den USA und Europa zeigen das Vorhandensein von LNPs
Diese internationale Durchsetzung erweitert das laufende Verfahren in den USA in Delaware
wo ein Geschworenenprozess für September 2025 angesetzt ist
die für die Lieferung von mRNA-Medikamenten wichtig ist
wurde von Wissenschaftlern von Arbutus und Genevant entwickelt und an verschiedene Dritte lizenziert
This expanded patent litigation represents a significant escalation in Arbutus and Genevant's enforcement strategy
By filing in multiple strategic jurisdictions—Canada
and the Unified Patent Court covering 27 European countries—they've created a comprehensive legal net targeting 30 countries simultaneously
The litigation focuses on lipid nanoparticle (LNP) technology
the critical delivery system that enables mRNA therapeutics to function by protecting the mRNA and facilitating cellular uptake
What strengthens their position is the submission of physical evidence from testing commercial Moderna samples
suggesting they've conducted due diligence before filing
The request for both monetary damages and injunctive relief is particularly aggressive
the threat of injunctions creates substantial leverage
as it could potentially force Moderna's products off market in multiple territories
The UPC filings are especially significant as they streamline enforcement across numerous European markets simultaneously
This multi-jurisdictional approach accomplishes several strategic objectives: it increases settlement pressure
and creates the possibility for favorable rulings in some jurisdictions to influence others
these international filings create additional pressure points that could accelerate settlement discussions rather than risk adverse rulings across multiple markets
This expanded patent enforcement campaign significantly enhances Arbutus's potential for substantial financial recovery and strengthens its position in the LNP technology marketplace
The litigation targets not just Spikevax but potentially other Moderna products using similar LNP technology
this aggressive patent strategy highlights that Arbutus's intellectual property portfolio may be undervalued relative to its fundamental importance in enabling mRNA therapeutics
The company appears confident in the strength of its patents
evidenced by the investment in simultaneous multi-jurisdictional litigation
The financial implications extend beyond potential damages from Moderna
A successful outcome would validate Arbutus's patent portfolio
potentially increasing licensing revenue from other pharmaceutical companies developing mRNA therapies
This could transform Arbutus from being valued primarily on its clinical pipeline to recognition as a key technology enabler in the mRNA space
this litigation introduces both opportunity and risk
and litigation outcomes are inherently unpredictable
the comprehensive approach suggests a strong conviction in their legal position
The most significant near-term catalyst will be the U.S
though developments in any of these international cases could trigger settlement discussions sooner
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Initiating Phase 2b clinical trial in first half of 2025 after achieving a meaningful functional cure rate in cHBV patients treated with imdusiran and interferon
a clinical-stage biopharmaceutical company leveraging its extensive virology expertise to develop a functional cure for people with chronic hepatitis B virus (cHBV) infection
today announced its 2025 corporate objectives and provided a financial update
“We enter 2025 with solid financial footing and strong momentum in achieving our mission of developing a functional cure for cHBV
a disease that affects more than 250 million people worldwide and is a leading cause of liver cancer,” said Michael J
Interim President and Chief Executive Officer of Arbutus
“The data we reported late last year from our IM-PROVE I Phase 2a clinical trial showed a meaningful functional cure rate and immune activation in cHBV patients that were treated with our RNAi therapeutic
interferon and nucleos(t)ide analogue (NA) therapy
These data support our belief that imdusiran is differentiated from other RNAi therapeutics in development for HBV
we plan to initiate a Phase 2b clinical trial combining imdusiran
interferon and NA therapy in the first half of 2025.”
the Company is planning to initiate a Phase 2b clinical trial of imdusiran combined with IFN and NA therapy
AB-101 is our oral PD-L1 inhibitor candidate that we believe will allow for controlled checkpoint blockade while minimizing the systemic safety issues typically seen with checkpoint antibody therapies
when used in combination with other approved and investigational agents
could potentially lead to a functional cure in patients chronically infected with HBV
Forward-looking statements in this press release include statements about: the potential to lead to a functional cure for HBV; Arbutus’ future development plans for its product candidates; the expected timing
cost and results of Arbutus’ clinical development plans and clinical trials with respect to its product candidates; Arbutus’ expectations with respect to the cost
initiation and the release of data from its clinical trials and the expected timing thereof; the potential for Arbutus’ product candidates to achieve success in clinical trials; Arbutus’ expectations with respect to utilizing its ATM program; Arbutus’ plans with respect to the ongoing patent litigation matters; and Arbutus’ expected financial condition
including the anticipated duration of its cash runway
its expectations regarding its 2025 cash burn and the timing and need for additional capital
or investor perceptions; and risks related to the sufficiency of Arbutus’ cash resources and its ability to obtain adequate financing in the future for its foreseeable and unforeseeable operating expenses and capital expenditures
Lisa M. CaperelliVice President, Investor Relations Phone: 215-206-1822 Email: lcaperelli@arbutusbio.com
We’re fighting for improved benefits and fair wages that keep pace with the cost of living
Ninety-five per cent of union employees at the Arbutus Club earn less than the Living Wage—the salary required in Vancouver for two working parents to meet the basic needs of a family of four
Unifor members vote for strike action if necessary at Arbutus Club
Arbutus Biopharma (Nasdaq: ABUS) announced significant leadership changes
appointing Lindsay Androski as Chief Executive Officer
replacing Interim President and CEO Michael J
an MIT-trained biologist with nearly 30 years of experience in biotechnology
will also join the company's board of directors
The clinical-stage biopharmaceutical company has also appointed four new directors to its board: Robert Alan Beardsley
All previous board members have stepped down
The company may consider adding directors with clinical development expertise in the coming months
Androski stated that these leadership changes aim to enable "renewed focus on advancing the company's pipeline efficiently and maximizing the company's contributions to LNP delivery technology through Genevant." The company will temporarily pause investor meetings while the new leadership reviews development plans and strategic options for its hepatitis B programs
Arbutus Biopharma (Nasdaq: ABUS) ha annunciato significative modifiche nella leadership
nominando Lindsay Androski come Amministratore Delegato
che sostituisce il Presidente e CEO ad interim Michael J
biologa formata al MIT con quasi 30 anni di esperienza nei settori della biotecnologia
entrerà anche a far parte del consiglio di amministrazione dell'azienda
La società biofarmaceutica in fase clinica ha anche nominato quattro nuovi membri nel suo consiglio: Robert Alan Beardsley
Tutti i membri precedenti del consiglio si sono dimessi
riducendo il consiglio a un totale di cinque membri
L'azienda potrebbe considerare di aggiungere direttori con esperienza nello sviluppo clinico nei prossimi mesi
Androski ha dichiarato che queste modifiche nella leadership mirano a consentire un "rinnovato focus sull'avanzamento del pipeline dell'azienda in modo efficiente e a massimizzare i contributi dell'azienda alla tecnologia di somministrazione LNP attraverso Genevant." L'azienda sospenderà temporaneamente gli incontri con gli investitori mentre la nuova leadership rivede i piani di sviluppo e le opzioni strategiche per i suoi programmi contro l'epatite B
Arbutus Biopharma (Nasdaq: ABUS) anunció cambios significativos en su liderazgo
nombrando a Lindsay Androski como Directora Ejecutiva
reemplazando al Presidente y CEO interino Michael J
bióloga formada en el MIT con casi 30 años de experiencia en biotecnología
también se unirá a la junta directiva de la empresa
La compañía biofarmacéutica en etapa clínica también ha nombrado a cuatro nuevos directores en su junta: Robert Alan Beardsley
Todos los miembros anteriores de la junta han renunciado
reduciendo la junta a un total de cinco miembros
La empresa podría considerar la adición de directores con experiencia en desarrollo clínico en los próximos meses
Androski declaró que estos cambios en el liderazgo tienen como objetivo permitir un "nuevo enfoque en avanzar la cartera de la empresa de manera eficiente y maximizar las contribuciones de la empresa a la tecnología de entrega de LNP a través de Genevant." La empresa pausará temporalmente las reuniones con inversores mientras el nuevo liderazgo revisa los planes de desarrollo y las opciones estratégicas para sus programas de hepatitis B
Arbutus Biopharma (Nasdaq: ABUS)는 주요 리더십 변화를 발표하며 Lindsay Androski를 CEO로 임명하고
임상 단계의 생물 의약품 회사는 이사회에 네 명의 새로운 이사를 추가로 임명했습니다: Robert Alan Beardsley
회사는 향후 몇 달 내에 임상 개발 전문성을 가진 이사를 추가하는 것을 고려할 수 있습니다
Androski는 이러한 리더십 변화가 "회사의 파이프라인을 효율적으로 발전시키고 Genevant를 통한 LNP 전달 기술에 대한 회사의 기여를 극대화하는 데 새롭게 집중할 수 있도록" 하기 위한 것이라고 밝혔습니다
회사는 새로운 리더십이 B형 간염 프로그램에 대한 개발 계획과 전략적 옵션을 검토하는 동안 투자자 회의를 일시적으로 중단할 것입니다
Arbutus Biopharma (Nasdaq: ABUS) a annoncé des changements significatifs dans sa direction
nommant Lindsay Androski au poste de Directrice Générale
remplaçant le Président et CEO par intérim Michael J
biologiste formée au MIT avec près de 30 ans d'expérience en biotechnologie
rejoindra également le conseil d'administration de l'entreprise
L'entreprise bio-pharmaceutique en phase clinique a également nommé quatre nouveaux administrateurs à son conseil : Robert Alan Beardsley
Tous les membres précédents du conseil ont démissionné
réduisant le conseil à un total de cinq membres
L'entreprise pourrait envisager d'ajouter des administrateurs ayant une expertise en développement clinique dans les mois à venir
Androski a déclaré que ces changements de leadership visent à permettre un "nouveau focus sur l'avancement efficace du pipeline de l'entreprise et à maximiser les contributions de l'entreprise à la technologie de livraison LNP à travers Genevant." L'entreprise suspendra temporairement les réunions avec les investisseurs pendant que la nouvelle direction examine les plans de développement et les options stratégiques pour ses programmes de lutte contre l'hépatite B
Arbutus Biopharma (Nasdaq: ABUS) hat bedeutende Veränderungen in der Unternehmensführung angekündigt und Lindsay Androski zur Geschäftsführerin ernannt
die den interimistischen Präsidenten und CEO Michael J
eine am MIT ausgebildete Biologin mit fast 30 Jahren Erfahrung in Biotechnologie
wird auch dem Vorstand des Unternehmens beitreten
Das biopharmazeutische Unternehmen in der klinischen Phase hat außerdem vier neue Direktoren in seinen Vorstand berufen: Robert Alan Beardsley
Alle vorherigen Vorstandsmitglieder haben ihren Rücktritt erklärt
wodurch der Vorstand auf insgesamt fünf Mitglieder reduziert wurde
Das Unternehmen könnte in den kommenden Monaten die Hinzufügung von Direktoren mit Fachwissen in der klinischen Entwicklung in Betracht ziehen
dass diese Veränderungen in der Führung darauf abzielen
einen "neuen Fokus auf die effiziente Weiterentwicklung der Unternehmenspipeline und die Maximierung der Beiträge des Unternehmens zur LNP-Abliefertechnologie durch Genevant" zu ermöglichen
Das Unternehmen wird vorübergehend die Investorenmeetings aussetzen
während die neue Führung die Entwicklungspläne und strategischen Optionen für die Programme zur Bekämpfung von Hepatitis B überprüft
has died in a one-alarm apartment fire in Arbutus
according to the Baltimore County Fire Department
the fire crew responded to a report of an apartment fire at the 4400 block of Alan Drive
Authorities reported that another rescue crew was dispatched after the resident told the 911 operator that he could not escape
ALSO READ| Amazon vehicle stolen in Northeast Baltimore, eventually recovered
the fire crew learned the fire was coming from the second floor of the apartment
Investigators ruled the fire to be accidental from unattended cooking
50% of patients who had baseline HBsAg levels less than 1000 IU/mL achieved functional cure in Cohort A1 of the IM-PROVE I Phase 2a clinical trial
Data to be presented in late-breaker poster session at AASLD – The Liver Meeting® on Monday
2024 (GLOBE NEWSWIRE) -- Arbutus Biopharma Corporation (Nasdaq: ABUS) (“Arbutus” or the “Company”)
today announced new data from its IM-PROVE I Phase 2a clinical trial (AB-729-201) showing that six doses of imdusiran
and 24 weeks of pegylated interferon alfa-2α (IFN)
added to ongoing nucleos(t)ide analogue (NA) therapy
led to a functional cure rate of 50% (3/6) in HBeAg-negative patients with baseline HBsAg levels less than 1000 IU/mL
and an overall functional cure rate of 25% (3/12)
Patients with HBsAg levels less than 1000 IU/mL represent a significant portion of the cHBV population
These data will be presented as a late-breaker poster presentation on November 18
2024 at The American Association for the Study of Liver Diseases (AASLD) – The Liver Meeting® 2024
we are seeing a meaningful percentage of HBV patients functionally cured with an RNAi therapeutic and interferon,” commented Professor Man-Fung Yuen
Chief of the Division of Gastroenterology and Hepatology
the University of Hong Kong and Principal Investigator of the IM-PROVE I clinical trial
“While 48 weeks of interferon can be used as a standard of care treatment for HBV patients
historically less than 10% of patients experience a functional cure
with the combination of imdusiran and 24 weeks of interferon
we see a 50% functional cure rate in HBV patients with HBsAg less than 1000 IU/mL at baseline and a 25% functional cure rate overall
I was pleased to see that this regimen with a short course of interferon was generally safe and well-tolerated
These data are extremely impressive and provide hope for the millions of HBV patients worldwide and the medical community that a finite curative treatment is possible with imdusiran and interferon.”
Key data from patients in Cohort A1 that received 6 doses of imdusiran plus 24 weeks of IFN in addition to ongoing NA therapy include:
“IM-PROVE I: Imdusiran in Combination with Short Courses of Pegylated Interferon Alfa-2a in Virally Suppressed
HBeAg Negative Subjects with Chronic HBV (cHBV) Infection Leads to Functional Cure”
is available on the Company’s website and provides the complete data set for all four cohorts of patients dosed in this clinical trial
Additional immune activation data in those patients in Cohort A1 that achieved a functional cure will be presented by Dr
Immunobiology and Biomarkers Research at Arbutus Biopharma in a poster titled
“Soluble Immune Biomarker Profiling of Chronic Hepatitis B Subjects Treated with Imdusiran in Combination with Pegylated Interferon Alfa Reveals Phases of Immune Activation.” The data in this poster show that patients in Cohort A1 had greater increases in favorable immune biomarkers than those in other cohorts
Functionally cured patients and those with baseline HBsAg <1000 IU/mL had elevations of key immune biomarkers during the imdusiran lead-in
suggesting immune activation induced by imdusiran plus IFN treatment
“We are extremely excited to have functionally cured these patients with the imdusiran and interferon treatment regimen
There is a significant need for a functional cure for the more than 250 million patients chronically infected with HBV worldwide,” commented Dr
Chief Medical Officer of Arbutus Biopharma
“Excess production of surface antigen is believed to contribute to host immune exhaustion
resulting in inadequate immune response and failure to suppress the virus
These data support our belief that lowering surface antigen with imdusiran and incorporating an immunomodulator in the treatment regimen provides a functional cure in some patients with cHBV
We thank all the patients and investigators who participated in this clinical trial.”
All of the above posters that will be presented at AASLD – The Liver Meeting can be accessed through the Arbutus website under Publications
The IM-PROVE I Phase 2a Clinical trial (AB-729-201; NCT04980482) enrolled 43 HBeAg-negative
NA-suppressed patients with cHBV infection
After a 24-week lead-in with imdusiran (60 mg every 8 weeks
patients were randomized into one of the following four cohorts: Cohort A1: imdusiran (2 doses) + NA + IFN weekly for 24 weeks (n=12)
Cohort A2: NA + IFN weekly for 24 weeks (n=13)
Cohort B1: Imdusiran (1 dose) + NA + IFN weekly for 12 weeks (n=8) and Cohort B2: NA + IFN weekly for 12 weeks (n=10)
After completion of the IFN treatment period (Week 52 for cohorts A1 and A2 and Week 40 for cohorts B1 and B2)
patients underwent a 24-week follow-up period on NA therapy alone and were then assessed for discontinuation of NA therapy
Patients with ALT levels less than two times the upper limit of normal
and HBsAg <100 IU/mL at two consecutive visits at least 24 weeks after the last dose of imdusiran qualified to discontinue all therapy and will be followed for at least 48 weeks
Imdusiran is an RNA interference (RNAi) therapeutic specifically designed to reduce all HBV viral proteins and antigens including hepatitis B surface antigen
imdusiran achieved meaningful functional cure rates in patients with cHBV when combined with pegylated interferon alfa-2α and nucleos(t)ide analogue therapy
Additional clinical data generated thus far has shown imdusiran to be generally safe and well-tolerated
Plans are underway to advance imdusiran into a Phase 2b clinical trial
Forward-Looking Statements and Information
Forward-looking statements in this press release include statements about: the IM-PROVE I Phase 2a clinical trial data; the potential for finite curative treatment to be possible with imdusiran
among other things: the effectiveness and timeliness of preclinical studies and clinical trials
among others: anticipated pre-clinical studies and clinical trials may be more costly or take longer to complete than anticipated
or may not generate results that warrant future development of the tested product candidate; Arbutus may elect to change its strategy regarding its product candidates and clinical development activities; Arbutus may not receive the necessary regulatory approvals for the clinical development of Arbutus’ products; economic and market conditions may worsen; market shifts may require a change in strategic focus
Lisa M. Caperelli Vice President, Investor Relations Phone: 215-206-1822 Email: lcaperelli@arbutusbio.com
serious injury crash this weekend on Interstate 95 in Baltimore County
Troopers said the wreck happened Sunday around 2:50 a.m
A 2008 Mercury Mountaineer SUV hit the back of a 2004 tractor-trailer
Police said a 2016 Toyota Corolla sedan then hit the Mercury
The Mercury and Toyota drivers were both taken to the University of Maryland R Adams Cowley Shock Trauma Center in Baltimore
The Maryland State Police is still investigating
Charges are pending the outcome of the investigation and a consultation with the Office of the State's Attorney in Baltimore County
This map shows the area where authorities said the crash happened
HBV therapies developer Arbutus Biopharma Corp. (NASDAQ:ABUS) has named Lindsay Androski CEO and replaced its entire board
Androski is special counsel at Genevant Sciences Corp.
an RNA therapeutics company set up by Arbutus and Roivant Sciences Ltd
(NASDAQ:ROIV) in 2018 to advance treatments using Arbutus’ liquid nanoparticle and ligand conjugation technologies
who had been Arbutus’ interim president and CEO since the start of 2024
has resigned from the board along with Daniel Burgess
Arbutus said the new team will review its development plans and strategic options for its HBV programs while “maximizing the company's contributions to LNP delivery technology through Genevant.”..
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spans two separate parcels totaling 7.88 acres
It is home to a tenant mix of national brands such as Walgreens
in addition to various local service-oriented businesses
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On January 27, 2022, Betty Arbutus (Arby) Harmon Brannon died peacefully in her home, surrounded by her four children. She was 93 years old. She was born on September 9, 1928, in Bessemer City, North Carolina, to the late Russell and Irene Harmon.... View Obituary & Service Information
The family of Betty Arbutus (Arby) Brannon created this Life Tributes page to make it easy to share your memories
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The demand for nontimber forest products (NTFPs) has increased significantly in recent years
Hundreds of plant species that grow naturally in Türkiye have medicinal and aromatic value
Medicinal and aromatic plants are primarily used as a sources of tea
are used for decorative purposes and as fuel wood in many wood-based industries
they also have a wide range of uses in packaging
the fruits of these trees are widely consumed by humans and animals because they are rich in sugar and vitamin C
It is predicted that changes in climatic conditions will significantly change the distribution
composition and function of forests threatening biodiversity
The purpose of this study was to model current and future potential geographical distributions of Arbutus unedo L.
which is among the species that naturally grow in Türkiye and is of substantial value in terms of its ecological contribution to forest ecosystems
based on species presence data and environmental variables (bioclimatic variables and altitude)
The current and future distribution area models for Arbutus unedo L
indicate that the potential distribution areas of the species in the coming years will gradually decrease
which represents the highest level of world resource usage this gradual decrease will reach its highest level and there will be no suitable distribution area left for the species
it is predicted that the species will become endangered
In-situ and ex-situ conservation measures need to be taken to ensure the sustainability of the species in forestry and landscape areas
The SSPs created for the models are based on five narratives that describe broad socioeconomic trends that may shape future societies
predicting how socioeconomic conditions will affect the implementation of climate policy
represents a moderate level of mitigation and adaptation
and SSP5 represents a high level of use of fuel and world resources
The algorithm takes the projection of the sample points on climatic variables
yields the attribute information of the species in those areas and determines points suitable for the species based on the determined attributes by randomly assigning points in the background
Areas that have similar attributes in the obtained and future projection data are considered suitable distribution areas for the species
10000 background points were used according to the area size
The variables used in the newly created model were BIO 2
Two different models were constructed for two shared socioeconomic pathways (SSP2-4.5 and SSP5-8.5) under greenhouse warming scenarios
All variable rasters were at a 30 arc-second resolution
Five classifications were made for maps of potential distribution areas (0 is not suitable
0.50–0.75 is suitable and 0.75–1.0 is very suitable)
the maps obtained as raster were converted into vector format
and the areal coverage is presented in tables
Predictive accuracy of the model variables the Jackknife test
Potential distribution of Arbutus unedo—created using QGIS v3.2435.
The existing data and the model created for the current study were consistent
The distribution area of Arbutus unedo is on the coast of the country
and its current distribution is far northwards on the northern coast of Marmara sea
in the models created for the distribution areas for the years 2041–2060 and 2081–2100
unedo will start to withdraw from the Mediterranean and Aegean regions
where it already has a limited distribution
and its distribution will shift to the northern parts of the Marmara region
the presence of very suitable distribution areas for the species in the northern areas will be severely restricted
which has a wide distribution in our country
with MaxEnt; the model output suggested that the species distribution areas will shrink in the future
Since the ethnobotanical and food use of this species is widespread in Türkiye
and as long as this level of use of the Earth’s resources continues
extinction will be inevitable for the Strawberry tree and many other species
Climate change is important from a wide variety of perspectives
from the distribution of plant species to their protection and use
The MaxEnt model predicted significant fluctuations in A
unedo distribution areas in Türkiye over the next 50 years
unedo are not significantly affected in the SSP2-4.5 projection from climate change
there is a significant decrease in the distribution area of this species in the SSP5-8.5 projection
this study conducted at the geographical boundaries of Türkiye showed that the distribution of Strawberry trees in the coming years will gradually decrease and the species will become more threatened
will not be maintained in the Aegean strip in the future
and will decrease by shifting to the northern latitudes in the western Black Sea and Marmara regions
will shift its distribution to northern latitudes
not only in Türkiye but also in other Mediterranean countries
To avoid economic and ecological losses related to Strawberry trees
it is important to conduct studies on a global scale rather than on local scales to ensure the future of Strawberry trees
No new data were created or analysed in this study
Data sharing is not applicable to this article
The data presented in this study are available upon request from the corresponding author
Uzun, A. & Sarikaya, A. G. Estimation of current and future potential distribution areas of Pistacia terebinthus L. by random forest regression algorithm. Artvin Coruh Univ. J. For. Fac. 24(2), 160–169. https://doi.org/10.17474/artvinofd.1298275 (2023)
Abdelaal, M., Fois, M., Fenu, G. & Bacchetta, G. Using MaxEnt modeling to predict the potential distribution of the endemic plant Rosa arabica crép in Egypt. Ecol. Inform. 50, 68–75. https://doi.org/10.1016/j.ecoinf.2019.01.003 (2019)
Distribution of rose hip (Rosa canina L.) under current and future climate conditions
Li, G., Huang, J., Guo, H. & Du, S. Projecting species loss and turnover under climate change for 111 Chinese tree species. For. Ecol. Manage. 477, 118488. https://doi.org/10.1016/j.foreco.2020.118488 (2020)
Chakraborty, A., Joshi, P. K. & Sachdeva, K. Predicting distribution of major forest tree species to potential impacts of climate change in the central Himalayan region. Ecol. Eng. 97, 593–609. https://doi.org/10.1016/j.ecoleng.2016.10.006 (2016)
Zhao, H., Zhang, H. & Xu, C. Study on Taiwania cryptomerioides under climate change: MaxEnt modeling for predicting the potential geographical distribution. Glob. Ecol. Conserv. 24, e01313. https://doi.org/10.1016/j.gecco.2020.e01313 (2020)
Dyderski, M. K., Paź, S., Frelich, L. E. & Jagodziński, A. M. How much does climate change threaten European forest tree species distributions?. Glob. Change Biol. 24, 1150–1163. https://doi.org/10.1111/gcb.13925 (2018)
Zhang, K., Yao, L., Meng, J. & Tao, J. Maxent modeling for predicting the potential geographical distribution of two peony species under climate change. Sci. Total Environ. 634, 1326–1334. https://doi.org/10.1016/j.scitotenv.2018.04.112 (2018)
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This research was funded by Turkish Scientific Council (TÜBİTAK) 2209 project
is a scholar in the field of “Sustainable Forestry and Forest Disasters” within the scope of YÖK 100/2000 project)
Ayse Gul Sarikaya and Almira Uzun performed background research and designed the study
Ayse Gul Sarikaya and Funda Dila Turan obtained the data and analysed them
The modelling results were reviewed by Almira Uzun
All authors discussed the results and commented on the manuscript
The order of the authors is based on the level of their contribution
The authors declare no competing interests
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations
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