Assembly Biosciences will present clinical data on ABI-6250, a hepatitis D entry inhibitor, at the EASL Congress.
Quiver AI Summary
Assembly Biosciences, Inc. announced that it will present topline clinical data for ABI-6250, an investigational oral entry inhibitor for hepatitis D virus (HDV), at the upcoming EASL Congress in Barcelona, Spain, from May 27-30, 2026. This data, from a Phase 1a study assessing the safety and pharmacokinetics of ABI-6250, is significant as it represents the only oral entry inhibitor currently being tested for chronic HDV. Anuj Gaggar, the company's chief medical officer, expressed optimism about advancing to a Phase 2 study by the end of the year based on these findings. The presentation will provide interim results and will be made available on the company's website following the conference. As a reminder, ABI-6250 is still in development and has not yet been approved for use.
Potential Positives
- Assembly Biosciences will present topline clinical data on ABI-6250, an investigational oral hepatitis D virus entry inhibitor, at the prestigious European Association for the Study of the Liver (EASL) Congress, highlighting its credibility and visibility in the field.
- ABI-6250 is positioned as the only oral entry inhibitor currently in clinical development for chronic hepatitis D, potentially establishing a unique market advantage for Assembly Biosciences.
- The company plans to advance ABI-6250 directly into a Phase 2 study by year-end, indicating confidence in the product's development progress and potential future commercialization.
- The presentation will feature results from a randomized, blinded, Phase 1a study, showcasing a robust clinical trial design that may enhance the confidence of investors and stakeholders in the company's pipeline.
Potential Negatives
- The investigational therapy ABI-6250 has not been approved globally, and its safety and efficacy have not been established, indicating a significant risk for the company's future success.
- The reliance on the upcoming Phase 2 study is uncertain, as the company acknowledges that clinical and nonclinical data may not warrant further development of its product candidates.
- The press release includes multiple forward-looking statements that emphasize potential risks and uncertainties, which could negatively impact investor confidence and perception of the company’s stability.
FAQ
What is ABI-6250?
ABI-6250 is an investigational oral entry inhibitor targeting hepatitis D virus (HDV), currently in clinical development by Assembly Biosciences.
When will ABI-6250 data be presented?
The topline clinical data on ABI-6250 will be presented at the EASL Congress from May 27-30, 2026.
What phase of clinical study is ABI-6250 currently in?
ABI-6250 is undergoing a Phase 1a study, with plans to advance to Phase 2 by year-end 2026.
Where can I find the poster presentation for ABI-6250?
The poster will be available on the "Events & Presentations" and "Publications" pages of Assembly Bio's website.
Is ABI-6250 approved for use globally?
No, ABI-6250 is an investigational product that has not been approved anywhere globally, and its safety and efficacy are not yet established.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$ASMB Insider Trading Activity
$ASMB insiders have traded $ASMB stock on the open market 4 times in the past 6 months. Of those trades, 0 have been purchases and 4 have been sales.
Here’s a breakdown of recent trading of $ASMB stock by insiders over the last 6 months:
- JEANETTE M BJORKQUIST (PFO and PAO) has made 0 purchases and 2 sales selling 328 shares for an estimated $8,754.
- NICOLE S WHITE (Chief Manufacturing Officer) has made 0 purchases and 2 sales selling 197 shares for an estimated $5,257.
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$ASMB Hedge Fund Activity
We have seen 42 institutional investors add shares of $ASMB stock to their portfolio, and 23 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- PARADIGM BIOCAPITAL ADVISORS LP added 665,251 shares (+inf%) to their portfolio in Q4 2025, for an estimated $22,625,186
- FRAZIER LIFE SCIENCES MANAGEMENT, L.P. removed 456,249 shares (-100.0%) from their portfolio in Q4 2025, for an estimated $15,517,028
- POINT72 ASSET MANAGEMENT, L.P. added 304,592 shares (+102.9%) to their portfolio in Q4 2025, for an estimated $10,359,173
- EVERSEPT PARTNERS, LP added 159,676 shares (+inf%) to their portfolio in Q4 2025, for an estimated $5,430,580
- RENAISSANCE TECHNOLOGIES LLC removed 144,371 shares (-94.0%) from their portfolio in Q4 2025, for an estimated $4,910,057
- BLACKSTONE INC. removed 129,035 shares (-28.8%) from their portfolio in Q4 2025, for an estimated $4,388,480
- CAPTION MANAGEMENT, LLC added 106,591 shares (+inf%) to their portfolio in Q4 2025, for an estimated $3,625,159
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$ASMB Price Targets
Multiple analysts have issued price targets for $ASMB recently. We have seen 3 analysts offer price targets for $ASMB in the last 6 months, with a median target of $43.0.
Here are some recent targets:
- Patrick R. Trucchio from HC Wainwright & Co. set a target price of $50.0 on 05/04/2026
- Vamil Divan from Guggenheim set a target price of $43.0 on 04/06/2026
- Salim Syed from Mizuho set a target price of $40.0 on 11/20/2025
Full Release
SOUTH SAN FRANCISCO, Calif., May 13, 2026 (GLOBE NEWSWIRE) -- Assembly Biosciences, Inc. (Nasdaq: ASMB), a biotechnology company developing innovative therapeutics targeting serious viral diseases, today announced topline clinical data on ABI-6250, an investigational oral hepatitis D virus (HDV) entry inhibitor, will be presented in a poster presentation at the European Association for the Study of the Liver (EASL) Congress taking place May 27-30, 2026, in Barcelona, Spain.
“We are pleased to present additional Phase 1a data on ABI-6250 at EASL,” said Anuj Gaggar, MD, PhD, chief medical officer of Assembly Bio. “As the only oral entry inhibitor currently in clinical development for chronic hepatitis D, ABI-6250 is designed to offer a differentiated approach, and these data further support our plan to advance directly into a Phase 2 study by year-end.”
The presentation will feature results from a randomized, blinded, Phase 1a study evaluating the safety, pharmacokinetics and pharmacodynamic activity of ABI-6250 following single- and multiple-dose administration in healthy participants.
Presentation details are as follows:
Title:
Safety, Pharmacokinetics, and Pharmacodynamic Activity of ABI-6250, a First-in-Class Oral Hepatitis D Virus Entry Inhibitor, in Healthy Subjects: Interim Results From a Randomized, Blinded, Phase 1a Study
Presenter:
Edward J. Gane, MD, University of Auckland
Poster Number:
WED-579
Session:
Viral Hepatitis B and D: New therapies, unapproved therapies or strategies
Date:
Wednesday, May 27, 2026
Assembly Bio intends to make the poster available on the “Events & Presentations” page in the “Investors” section and on the “Publications” page in the “Pipeline” section of its website at www.assemblybio.com .
ABI-6250 is an investigational product candidate that has not been approved anywhere globally, and its safety and efficacy has not been established.
About Assembly Biosciences
Assembly Biosciences is a biotechnology company dedicated to the development of innovative small-molecule therapeutics designed to change the path of serious viral diseases and improve the lives of patients worldwide. Led by an accomplished team of leaders in virologic drug development, Assembly Bio is committed to improving outcomes for patients struggling with the serious, chronic impacts of herpesvirus, hepatitis B virus (HBV) and HDV infections. For more information, visit assemblybio.com.
Forward-Looking Statements
The information in this press release contains forward-looking statements that are subject to certain risks and uncertainties that could cause actual results to materially differ. These risks and uncertainties include: Assembly Bio’s ability to realize the potential benefits of its collaboration with Gilead, including all financial aspects of the collaboration and equity investments; Assembly Bio’s ability to initiate and complete clinical studies involving its therapeutic product candidates, including studies contemplated by Assembly Bio’s collaboration with Gilead, in the currently anticipated timeframes or at all; safety and efficacy data from clinical or nonclinical studies may not warrant further development of Assembly Bio’s product candidates; clinical and nonclinical data may not differentiate Assembly Bio’s product candidates from other companies’ candidates; Assembly Bio’s ability to maintain financial resources and secure additional funding necessary to continue its research activities, clinical studies, and other business operations; potential effects of changes in government regulation; results of nonclinical studies may not be representative of disease behavior in a clinical setting and may not be predictive of the outcomes of clinical studies; and other risks identified from time to time in Assembly Bio’s reports filed with the U.S. Securities and Exchange Commission (the SEC). You are urged to consider statements that include the words may, will, would, could, should, might, believes, hopes, estimates, projects, potential, expects, plans, anticipates, intends, continues, forecast, designed, goal or the negative of those words or other comparable words to be uncertain and forward-looking. Assembly Bio intends such forward-looking statements to be covered by the safe harbor provisions contained in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. More information about Assembly Bio’s risks and uncertainties are more fully detailed under the heading “Risk Factors” in Assembly Bio’s filings with the SEC, including its most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K. Except as required by law, Assembly Bio assumes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise.
Contacts:
Investors:
Patrick Till
Meru Advisors
(484) 788-8560
[email protected]
Media:
Sam Brown LLC
Jamie Strachota
(703) 819-7647
[email protected]