RecruitingPhase 2NCT07219459

Visugromab, Nivolumab and Lenvatinib Compared to Double Placebo and Lenvatinib in Unresectable or Metastatic Hepatocellular Carcinoma Post Anti-PD-(L)1 Failure

A Phase 2b, Randomized, Blinded Trial Investigating the Efficacy and Safety of Visugromab in Combination With Nivolumab and Lenvatinib Compared to Double Placebo and Lenvatinib in Participants With Unresectable or Metastatic Hepatocellular Carcinoma and Compensated Liver Function (Child-Pugh A) After Failure of First-Line Treatment That Included an Approved Anti PD-(L)1 Compound (GDFATHER HCC-01)


Sponsor

CatalYm GmbH

Enrollment

104 participants

Start Date

Mar 19, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This is a Phase 2b, randomized, blinded clinical trial investigating the efficacy and safety of visugromab in combination with nivolumab and Lenvatinib compared to double placebo and Lenvatinib in participants with unresectable or metastatic HCC and compensated liver function (Child-Pugh A) after failure of 1L treatment that included an anti-PD-(L)1 compound. The trial consists of 2 Parts: a non-randomized Safety-run-in part (Part 1) and the subsequent randomized part (Part 2) with 2 treatment arms (A and B). Randomization of participants into Treatment Arm A and B will continue until 40 efficacy-evaluable participants are enrolled into each Treatment Arm.


Eligibility

Min Age: 18 YearsMax Age: 100 Years

Inclusion Criteria7

  • Histologically confirmed diagnosis of unresectable or metastatic HCC, not amenable to a curative treatment approach.
  • Measurable disease as per RECIST v1.1 as determined by the Investigator based upon local radiologist assessment.
  • Must have failed one line of prior systemic treatment for unresectable or metastatic HCC containing an approved anti PD (L)-1 checkpoint inhibitor (CPI) with a minimum treatment duration of 12 weeks exposure for the CPI with no documented progression in this period.
  • Age ≥ 18 years on the day of signing the informed consent.
  • Life expectancy of at least 3 months as assessed by the Investigator.
  • ECOG performance status ≤1.
  • Child-Pugh score of A6 or better.

Exclusion Criteria12

  • Known fibrolamellar HCC, sarcomatoid HCC or mixed cholangiocarcinoma.
  • More than 1 line of prior systemic treatment for unresectable or metastatic HCC.
  • Received or completed any palliative radiotherapy for symptoms within 28 days of the first dose of IMP.
  • Expected to require any other form of antineoplastic therapy during the trial.
  • Clinically active inflammatory bowel disease, active diverticulitis, intra-abdominal abscess, and/or gastrointestinal obstruction.
  • Known history of other prior malignancy unless participant has undergone potentially curative therapy with no evidence of that disease recurrence for 5 years since initiation of that therapy.
  • Known or detected clinically active central nervous system (CNS) involvement by HCC or other tumors.
  • Have one of the following cardiovascular risk factors: myocardial infarction, peri/myocarditis, or history of ischemic stroke in the past 3 months before planned treatment start, uncontrolled heart failure, uncontrolled ventricular arrhythmia, QT interval corrected for heart rate using Fridericia's formula interval ≥ 470 ms regardless of sex.
  • An active autoimmune disease that has required systemic treatment in past 3 months before planned treatment start.
  • Comedication with metformin or metformin-containing antidiabetics in participants with type II diabetes.
  • Chronic systemic corticosteroid treatment for other reasons.
  • Prior liver or other organ transplantation.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BIOLOGICALVisugromab RDE (recommended dose for expansion)

Participants receive visugromab (RDE) intravenous (IV) on Day 1 of every 21-day cycle (every 3 weeks, or Q3W) for up to 35 treatments

BIOLOGICALNivolumab

Participants receive Nivolumab 360mg intravenous (IV) on Day 1 of every 21-day cycle (every 3 weeks, or Q3W) for up to 35 treatments after visugromab infusion

DRUGLenvatinib

Participants receive Lenvatinib per os (PO) once daily according to body weight (\> 60kg: 12mg; \< 60kg: 8mg)

OTHERPlacebo Saline Infusion

Saline (0.9%NaCl) intravenous (2x IV) on Day 1 of every 21-day cycle every 3 weeks (Q3W) for up to 35 treatments


Locations(2)

Universitätsklinikum Frankfurt Johann Wolfgang Goethe- Universität

Frankfurt, Germany

Asst Grande Ospedale Metropolitano Niguarda

Milan, Italy

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07219459