Enlivex will present positive Phase IIa data for Allocetra™ in knee osteoarthritis at ACR Convergence 2025.
Quiver AI Summary
Enlivex Therapeutics Ltd. announced its participation in the American College of Rheumatology Convergence 2025, where it will present a late-breaking poster on clinical data from its Phase IIa trial of Allocetra™ for treating moderate-to-severe knee osteoarthritis. The data, showcasing statistically significant improvements in pain reduction and functional outcomes, particularly in patients aged 60 and older, will be presented by renowned expert Prof. Philip Conaghan. The conference is taking place from October 24–29, 2025, in Chicago. Enlivex focuses on macrophage reprogramming immunotherapy, and its product, Allocetra™, aims to restore macrophages to their homeostatic state, crucial for immune system balance. Chief Medical Officer Einat Galamidi will also be present for discussions with stakeholders.
Potential Positives
- Presentation of positive Phase IIa clinical data at a prestigious medical conference may enhance the credibility and visibility of Enlivex's Allocetra™ therapy.
- Clinical results indicate statistically significant improvement in pain reduction and function in moderate-to-severe knee osteoarthritis patients, which could support further development and eventual market approval.
- Engagement with stakeholders and the scientific community at ACR Convergence 2025 may foster collaborations and investments in future research and development.
- Involvement of an esteemed expert, Prof. Philip Conaghan, in the presentation may attract attention from the medical community and increase confidence in the company’s research.
Potential Negatives
- The press release heavily emphasizes the potential of Allocetra™ but includes extensive forward-looking statements highlighting significant risks and uncertainties that may hinder the company's ability to generate revenues or successfully develop commercial products.
- Despite presenting positive clinical trial data, there is a caveat that results from early-stage trials may not be indicative of future success in later-stage trials, which could undermine investor confidence.
- There are multiple factors mentioned that could negatively impact the development of the Allocetra™ product line, such as unexpected safety and efficacy issues, which raises concerns about the stability of their pipeline.
FAQ
What is the focus of Enlivex Therapeutics' presentation at ACR Convergence 2025?
The presentation highlights clinical data for Allocetra™ in treating knee osteoarthritis, showcasing significant pain reduction and functional improvement.
Who is presenting the clinical data at the conference?
Prof. Philip Conaghan, a leader in osteoarthritis and musculoskeletal imaging, will present the data at ACR Convergence 2025.
When will the presentation take place?
The presentation is scheduled for October 28, 2025, from 10:30 AM to 12:30 PM CT.
What is Allocetra™ developed by Enlivex Therapeutics?
Allocetra™ is a universal cell therapy designed to reprogram macrophages to restore immune system balance and treat various severe conditions.
Where can I find more information about Enlivex Therapeutics?
More information can be found on Enlivex's official website at http://www.enlivex.com.
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.
$ENLV Hedge Fund Activity
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$ENLV Analyst Ratings
Wall Street analysts have issued reports on $ENLV in the last several months. We have seen 2 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- D. Boral Capital issued a "Buy" rating on 09/26/2025
- HC Wainwright & Co. issued a "Buy" rating on 09/02/2025
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$ENLV Price Targets
Multiple analysts have issued price targets for $ENLV recently. We have seen 2 analysts offer price targets for $ENLV in the last 6 months, with a median target of $10.0.
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Full Release
Ness-Ziona, Israel, Oct. 28, 2025 (GLOBE NEWSWIRE) -- Enlivex Therapeutics Ltd. (Nasdaq: ENLV, the “Company”), a clinical-stage macrophage reprogramming immunotherapy company, today announced that it will present a late-breaking poster abstract at the American College of Rheumatology (ACR) Convergence 2025, taking place October 24–29 at McCormick Place Convention Center in Chicago, Illinois.
The presentation will feature clinical data from the recently announced Phase IIa (ENX-CL-05-001) 3-month topline data readout for Allocetra™ in patients with moderate-to-severe knee osteoarthritis (KOA), including clinically meaningful and statistically significant improvement compared to the control placebo arm in reduction of pain and improvement of function, in idiopathic age-related osteoarthritis patients (≥60 years), representing more than 50% of the total KOA market and 54% of the study population, as well as new supporting biomarker data. The data will be presented by Prof. Philip Conaghan, Consultant Rheumatologist and Director of the NIHR Leeds Biomedical Research Centre. Professor Conaghan is an international leader in osteoarthritis and musculoskeletal imaging, who has authored more than 700 publications and chaired multiple global guidelines and trial initiatives.
Poster Presentation
- Title: Randomized, Double-Blind, Placebo-Controlled Phase IIa Trial of an Innovative Intra-Articular Apoptotic Cell Therapy in Knee Osteoarthritis (OA): 3-Month Positive Outcomes and Identification of Responder Population (NCT06233474)
- Abstract ID: 2220562
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    Date & Time:
   
   October 28, 2025 | 10:30 AM - 12:30 PM CT
   
 
Einat Galamidi, MD, CMO, will attend the conference and will be available for meetings with stakeholders and members of the scientific community.
ABOUT ENLIVEX
Enlivex is a clinical stage macrophage reprogramming immunotherapy company developing Allocetra™, a universal, off-the-shelf cell therapy designed to reprogram macrophages into their homeostatic state. Resetting non-homeostatic macrophages into their homeostatic state is critical for immune system rebalancing and resolution of life-threatening and life debilitating conditions. For more information, visit http://www.enlivex.com .
Safe Harbor Statement: This press release contains forward-looking statements, which may be identified by words such as “expects,” “plans,” “projects,” “will,” “may,” “anticipates,” “believes,” “should,” “would”, “could,” “intends,” “estimates,” “suggests,” “has the potential to” and other words of similar meaning, including statements regarding expected cash balances, market opportunities for the results of current clinical studies and preclinical experiments, the effectiveness of, and market opportunities for, ALLOCETRA TM programs. All such forward-looking statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Investors are cautioned that forward-looking statements involve risks and uncertainties that may affect Enlivex’s business and prospects, including the risks that Enlivex may not succeed in generating any revenues or developing any commercial products; that the products in development may fail, may not achieve the expected results or effectiveness and/or may not generate data that would support the approval or marketing of these products for the indications being studied or for other indications; that ongoing studies may not continue to show substantial or any activity; and other risks and uncertainties that may cause results to differ materially from those set forth in the forward-looking statements. The results of clinical trials in humans may produce results that differ significantly from the results of clinical and other trials in animals. The results of early-stage trials may differ significantly from the results of more developed, later-stage trials. The development of any products using the ALLOCETRA TM product line could also be affected by a number of other factors, including unexpected safety, efficacy or manufacturing issues, additional time requirements for data analyses and decision making, the impact of pharmaceutical industry regulation, the impact of competitive products and pricing and the impact of patents and other proprietary rights held by competitors and other third parties. In addition to the risk factors described above, investors should consider the economic, competitive, governmental, technological and other factors discussed in Enlivex’s filings with the Securities and Exchange Commission, including in the Company’s most recent Annual Report on Form 20-F filed with the Securities and Exchange Commission. The forward-looking statements contained in this press release speak only as of the date the statements were made, and we do not undertake any obligation to update forward-looking statements, except as required under applicable law.
  
   Contact:
  
  
  Dave Gentry, CEO
  
  RedChip Companies, Inc.
  
  1-407-644-4256
  
  
   
    [email protected]
   
  
 
 
         
       
       
    