MBRC-101 for Advanced Refractory Solid Tumors
This study is testing a new drug called MBRC-101, which is an antibody-drug conjugate (a targeted therapy that delivers a powerful drug directly to cancer cells). It's for people with advanced solid tumors that haven't responded to standard treatments. The main goals are to see if MBRC-101 is safe, how it moves through the body, and if it shows early signs of shrinking tumors. Researchers will also look at how long people live, how long their disease is controlled, and if their tumors shrink or disappear. You can join if you are 18 or older and have advanced cancer that hasn't responded to other treatments. The study is currently unclear on its recruitment status.
- Study design
- This is a first-in-human, open-label study with different phases (Phase 1, 1b, and 2) and plans to enroll about 130 participants. It's designed to find the best dose and then test the drug's effectiveness.
- What's involved
- You will need to provide written consent and be able to follow all study procedures. The study will monitor for side effects for up to 24 months, and dose-limiting toxicities will be evaluated over 21 days.
- Compensation
- Not stated in the trial record.
- Follow-up
- Safety will be monitored for up to 24 months after treatment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Safety, PK, and Preliminary Efficacy of MBRC-101 in Advanced Refractory Solid Tumors
At a glance
Conditions
Where it's being run
17 sites across 14 statesWho to contact
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What this trial measures
- Occurrence of treatment-emergent adverse events (TEAEs)Up to 24 Months
TEAEs will be graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v.5.0.
- Occurrence of dose limiting toxicities (DLTs) during the DLT evaluation period21 Days
The DLTs are specific adverse events and are defined as any of the following: high grade non-hematologic toxicity, or hematologic toxicity.