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NCT07291076RecruitingPhase 1/2

A Phase 1/2 Study of Pumitamig alone or in Combination with Ipilimumab in First-Line HCC

ROSETTA HCC-206: An Open-Label, Multi-Center, Randomized Phase 1/2 Study of Pumitamig Alone or In Combination with Ipilimumab in Participants with First-Line Advanced or Unresectable Hepatocellular Carcinoma (HCC)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 30 Oct 2026

Brief summary (registry, in English)

The main goal of phase 1 is to see if it is safe for people with liver cancer to take pumitamig with ipilimumab, and to find the best dose to use, while the main goal of phase 2 is to see how well treatment works better at shrinking liver cancer: pumitamig with ipilimumab and pumitamig alone.

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
47 (estimated)
First submitted
12 Dec 2025
Start date
13 May 2026
Lead sponsor
Bristol-Myers Squibb Services Unlimited Company
EU CT number
2025-523602-33-00

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 47
  • 20 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Other illness

  • People with rare types of liver cancer.
  • People who have serious bleeding problems or are likely to bleed easily.
  • People who have had an organ transplant or have immune system diseases.

Other

  • People with high blood pressure that can’t be controlled, even with medicine.
  • People whose urine has too much protein (sign of kidney problems).
  • People taking strong blood-thinning medicines.

Who the study is looking for

  • Age of Participant must be ≥ 18 years of age, or legal adult age according to the local regulation inclusive, at the time of signing the ICF.
  • People with a certain kind of advanced liver cancer (HCC) that can't be removed by surgery.
  • People who can still do most everyday things on their own.
  • People whose liver is working well.
  • People who haven't had certain treatments for their liver cancer before.
  • People who have at least one tumor that shows up on a scan.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (20)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitaetsklinikum Koeln AöR
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CologneGermanyRecruiting
Goethe University Frankfurt
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Frankfurt Am MainGermanyRecruiting
Universitaetsklinikum Schleswig-Holstein AöR
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LuebeckGermanyRecruiting
Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz KöR
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MainzGermanyRecruiting
Hospital Clinic de Barcelona
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BarcelonaSpainRecruiting
Hospital Universitario HM Sanchinarro
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MadridSpainRecruiting
Hospital General Universitario Gregorio Marañón
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MadridSpainRecruiting
Clinica Universidad de Navarra
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MadridSpainRecruiting
Clínica Universidad de navarra
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PamplonaSpainRecruiting
Assistance Publique Hopitaux De Paris
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Bobigny CedexFranceRecruiting
Centre Hospitalier Universitaire Grenoble Alpes
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Grenoble Cedex 9FranceRecruiting
Centre Hospitalier Universitaire De Montpellier
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Montpellier Cedex 5FranceRecruiting
Centre Hospitalier Universitaire de Bordeaux
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PessacFranceRecruiting
Centre Hospitalier Universitaire de Saint Etienne
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Saint-Priest-en-JarezFranceRecruiting
Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" - IRST S.r.l
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MeldolaItalyRecruiting
Ospedale San Raffaele S.r.l.
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MilanItalyRecruiting
Azienda Ospedaliero Universitaria Pisana
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PisaItalyRecruiting
Uniwersyteckie Centrum Kliniczne
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GdanskPolandNot yet recruiting
MTZ Clinical Research powered by Pratia
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WarsawPolandNot yet recruiting
Dolnośląskie Centrum Onkologii, Pulmonologii i Hematologii
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WroclawPolandNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.