A First-in-human Study to Learn About the Safety of BAY 3547926 and How Well it Works in Participants With Advanced Liver Cancer

Part of paid clinical trials in Duarte, California.

Sponsor
Bayer
Study ID
NCT06764316
Phase
PHASE1
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • BAY 3547926 — DRUG
    antibody conjugate with actinium-225 label
  • BAY 3547922 — DRUG
    antibody conjugate without actinium-225 label as preinjection
  • BAY 3713391 — DRUG
    Radioactive imaging agent - optional preinjection

Study Details

In this study, researchers want to learn about the safety of a new drug, BAY 3547926, and how well the drug works in people with a type of liver cancer called advanced hepatocellular carcinoma (HCC), which has a special protein called Glypican 3 (GPC3). Researchers want to find the best dose of BAY 3547926 for people with advanced HCC and look at the way the body absorbs and distributes the drug. The study drug, BAY 3547926, delivers a radioactive agent to cancer cells. The radioactive agent emits radiations which can damage the cancer cells and cause them to die. These radiations travel a small distance, so are expected to cause little damage to surrounding healthy tissues. This is the first study of BAY 3547926 in humans. Participants will take part in one of the 4 different parts of the study. In Part 1, participants will receive different doses of BAY 3547926 alone to find the dose that is deemed safe and works best for the participants. When this dose has been found, a larger number of participants will receive BAY 3547926 alone in Part 2 or with other treatments in Parts 3 and 4 of the study. During the study, the doctors and their study team will do health check-ups, take pictures (scans) of the body, collect blood and urine samples, and ask participants questions about how they are feeling and what health problems they are having.

Key Dates

Start date
Feb 28, 2025
Status verified
Jun 2026
Primary completion
Jul 31, 2029
Completion
Aug 31, 2031

Study Design

Enrollment
148 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Experimental: BAY 3547926
    actinium-225 labeled antibody conjugate

Primary Outcome Measure

Part 1 (dose escalation): Occurrence and severity of TEAEs [ Time Frame: up to 60 months after first administration ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
DuarteDuarteCalifornia91010-

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