– Hepion Represented as Authors in Preclinical and Clinical Posters Related to Rencofilstat and Cyclophilins –
EDISON, N.J., June 15, 2022 (GLOBE NEWSWIRE) — Hepion Pharmaceuticals, Inc. (NASDAQ:HEPA), a clinical mid-stage biopharmaceutical company focused on Artificial Intelligence (“AI”)-driven therapeutic drug development for the treatment of non-alcoholic steatohepatitis (“NASH”) and hepatocellular carcinoma (“HCC”), today announced that five abstracts have been accepted for poster presentations at the European Association for the Study of the Liver (EASL) International Liver Congress™ 2022 (ILC 2022) taking place June 22 – 26, 2022 in London, UK and digitally.
The accepted abstracts for poster presentations are as follows:
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Poster #: |
FRI590 |
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Title: |
Synergistic anti-tumor activity with a combination of anti-PD1 antibody and the cyclophilin inhibitor, rencofilstat, in the Hep53.4 fatty liver model of hepatocellular carcinoma |
|
Authors: |
D. Ure 1 , J. Leslie 3 , B. Variya 1 , R. Foster 1 , J. Mann 2 , D. Mann 2,3 |
|
Presenter: |
Dr. Daren Ure |
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Session: |
Liver tumours: Experimental and pathophysiology |
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Date: |
24/06/2022 |
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Time: |
09:00 – 18:00 |
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Poster #: |
FRI591 |
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Title: |
Rencofilstat, a pan-cyclophilin inhibitor, exerts diverse metabolic and transcriptional anti-tumor activities in a murine NASH-HCC model |
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Authors: |
D. Ure 1 , J. Kuo 4 , W. Stauffer 4 , L. Haddon 1 , C. Fu 1 , P. Mayo 1 , R. Foster 1 , P. Gallay 4 |
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Presenter: |
Dr. Daren Ure |
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Session: |
Liver tumours: Experimental and pathophysiology |
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Date: |
24/06/2022 |
|
Time: |
09:00 – 18:00 |
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Poster #: |
SAT130 |
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Title: |
Integrated transcriptomics of rencofilstat treatment in a Phase 2a NASH trial confirms anti-fibrotic effect of pan-cyclophilin inhibition and identifies rencofilstat-specific biomarkers |
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Authors: |
P. Mayo 1 , S. Harrison 5 , T. Hobbs 1 , D. Ure 1 , D. Trepanier 1 , E. Foster 1 , C. Zhao 1 , R. Foster 1 |
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Presenter: |
Dr. Patrick Mayo |
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Session: |
NFLD: Therapy |
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Date: |
25/06/2022 |
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Time: |
09:00 – 18:00 |
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Poster #: |
FRI568 |
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Title: |
Cyclophilin D knockout promotes cell death pathways in preventing HCC development in a streptozotocin-induced mouse model of diabetes-linked NASH |
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Authors: |
W. Stauffer 6 , J. Kuo 7 , M. Bobardt 6 , D. Ure 1 , R. Foster 1 , P. Gallay 6 |
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Presenter: |
Dr. Winston Stauffer |
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Session: |
Liver tumours: Experimental and pathophysiology |
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Date: |
24/06/2022 |
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Time: |
09:00 – 18:00 |
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Poster #: |
THU004 |
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Title: |
Cyclophilin inhibitor CRV431 as a potential therapy for Alcohol-related Liver Diseases |
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Authors: |
Elena Palma 8,9 , Sara Campinoti 8,9 , Una Rastovic 8,9 , Nicola Harris 8,9 , Omolola Ajayi 8,9 , Bruna Almeida 8,9 , Tsin Shue Koay 8,9 , Sandra Phillips 8,9 , Daren Ure 1 , Melissa Preziosi 10 , Rosa Miquel 10 , Andreas Prachalias 10 , Krishna Menon 10 , Nigel Heato 10 , Luca Urbani 8,9 , Shilpa Chokshi 8,9 |
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Presenter: |
Dr. Elena Palma |
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Session: |
Alcoholic Liver Disease |
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Date: |
23/06/2022 |
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Time: |
09:00 – 18:00 |
1
Hepion Pharmaceuticals;
2
FibroFind Ltd;
3
Newcastle University;
4
Scripps Research Institute;
5
Summit Clinical Research;
6
Department of Immunology & Microbiology, Scripps Research;
7
Arena Pharmaceuticals;
8
The Roger Williams Institute of Hepatology, Foundation for Liver Research;
9
King’s College London, Faculty of Life Sciences and Medicine;
10
Institute of Liver Studies, King’s College London
About Hepion Pharmaceuticals
The Company’s lead drug candidate, rencofilstat, is a potent inhibitor of cyclophilins, which are involved in many disease processes. Rencofilstat is currently in clinical-phase development for the treatment of NASH, with the potential to play an important role in the overall treatment of liver disease – from triggering events through to end-stage disease. Rencofilstat has been shown to reduce liver fibrosis and hepatocellular carcinoma tumor burden in experimental models of NASH, and has demonstrated antiviral activities towards HBV, HCV, and HDV through several mechanisms, in nonclinical studies. In November 2021, the U.S. Food and Drug Administration (“FDA”) granted Fast Track designation for rencofilstat for the treatment of NASH. That was soon followed in December 2021 by the FDA’s acceptance of Hepion’s investigational new drug (IND) application for rencofilstat for the treatment of hepatocellular carcinoma (HCC).
Hepion has created a proprietary AI platform, called AI-POWR™, which stands for
A
rtificial Intelligence –
P
recision Medicine;
O
mics (including genomics, proteomics, metabolomics, transcriptomics, and lipidomics);
W
orld database access; and
R
esponse and clinical outcomes. Hepion intends to use AI-POWR™ to help identify which NASH patients will best respond to rencofilstat, potentially shortening development timelines and increasing the delta between placebo and treatment groups. In addition to using AI-POWR™ to drive its ongoing NASH clinical development program, Hepion intends to use the platform to identify additional potential indications for rencofilstat to expand the company’s footprint in the cyclophilin inhibition therapeutic space.
For further information, please contact:
Stephen Kilmer
Hepion Pharmaceuticals Investor Relations
Direct: (646) 274-3580
[email protected]
