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COMPANY RESEARCH

Hepion → Panetta Partners

Rencofilstat (CRV431) has oral clinical studies in MASH. Hepion transferred related assets to Panetta in 2025; the record preserves the historical development and change in rights.

Company at a glance

Corporate information

Company entity
Hepion Pharmaceuticals, Inc.;excluding assets transferred to Panetta
Headquarters / principal office
Morristown, New JerseySelf-reported location on the company LinkedIn page; regional scope may differ from the legal or global headquarters. ↗
Founded
2013 ↗ ↗
Ownership / capital status
Publicly tradedPublicly traded (OTCQB: HEPA) ↗
Official corporate reference
https://hepionpharma.com/ ↗
LinkedIn company page
LinkedIn ↗ ↗
Latest financing / award identified
2026-08-03 · Public-company private placement · $3.055 million gross proceeds ↗

Financing of the Hepion entity, not financing of Panetta or the rencofilstat assets.

Profile review: 2026-11-04 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.

Disease tags match recorded text mentions and require program-level verification.

Technology, programs & evidence

Rencofilstat (CRV431) has oral clinical studies in MASH. Hepion transferred related assets to Panetta in 2025; the record preserves the historical development and change in rights.

Program / serviceTarget / indicationRepresentative stageEvidence & scope
rencofilstat / CRV431Cyclophilin · MASH / liver fibrosis历史临床 / 已转移Quantitative human results not confirmed in this review

Related news & literature

Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.

No cataloged update explicitly mentions this company.

Same-field reading (not company-specific)
Johnson & Johnson (PR Newswire)

Icotrokinra meets Phase 3 joint-response endpoint in biologic-naive psoriatic arthritis

Johnson & Johnson reported that 58% of patients receiving icotrokinra 200 mg achieved ACR20 at Week 16 in ICONIC-PsA 1, versus 41% with placebo. The oral IL-23 receptor peptide also showed skin responses. The company reported no new safety signals through Week 24; active psoriatic arthritis remains an investigational indication.

Entera Bio investor filing

Adjacent oral-peptide field: Entera reports $265.9 million cash as EB613 Phase 3 preparations continue

Entera reported $265.9 million in cash and cash equivalents at September 30, plus $6.5 million in restricted cash. Its November 6 update targets first site activation for an approximately 900-patient EB613 osteoporosis Phase 3 trial in late 2026. EB613 is an oral PTH(1-34) program, included here as an adjacent oral-peptide delivery development, not a cyclic-peptide candidate.

Johnson & Johnson

ICONIC-ASCEND reports icotrokinra noninferiority to ustekinumab in plaque psoriasis

Johnson & Johnson reported that ICONIC-ASCEND met its Week 16 co-primary endpoints: PASI 90 responses were 55.2% with icotrokinra versus 3.6% with placebo, and IGA 0/1 responses were 70.4% versus 9.5%. At Week 28, the oral peptide met noninferiority criteria versus ustekinumab across multiplicity-controlled key secondary skin-clearance endpoints.

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Sources & open questions

    1. Rencofilstat 资产转移至 Panetta ↗Hepion · SEC 8-K · 2025-05-26
    2. Rencofilstat 在 MASH 的原始临床研究 ↗Liver International · PubMed · 2025-03
    3. About Hepion ↗Hepion Pharmaceuticals · 2026
    4. Hepion company profile ↗Hepion / LinkedIn · Not stated
    5. Hepion FY2025 Form10-K ↗Hepion / SEC · 2026-03
    6. Hepion investor company information ↗Hepion Pharmaceuticals · Not stated
    7. Hepion Private Placement 8-K ↗Hepion / SEC · 2026-08
    8. Hepion Pharmaceuticals ↗Hepion Pharmaceuticals, Inc.;excluding assets transferred to Panetta · Accessed 2026-11-04; undated unless stated

    Inclusion is not endorsement or partner qualification. Assess company claims, clinical evidence, and project-specific capabilities separately.

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