Trial of JBZ-001 for Advanced Solid and Hematological Cancers
This study is testing a new oral capsule called JBZ-001 for people with advanced solid tumors (cancers that form solid masses) or hematological (blood) cancers that have come back or are not responding to standard treatments. The main goals are to see how safe JBZ-001 is, what side effects it might cause, and to find the highest dose that can be given safely. Researchers will also look at how the drug works in the body and if it shows any early signs of helping to treat the cancer. JBZ-001 is a type of drug called a checkpoint inhibitor. You may be able to join if you are 18 or older and have a solid tumor that has relapsed or is refractory (not responding to treatment), and for which standard treatments are not available or tolerated. The study is currently recruiting about 25 participants.
- Study design
- This is a Phase 1, open-label study, meaning both you and the study team will know which treatment you are receiving. It will involve a small number of participants, starting with 3 to 6 people at each dose level to find the safest and most effective dose.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The main safety and dose evaluations will be measured over 28 days. If you experience a benefit, you may continue treatment until your disease progresses or side effects become too severe.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Trial to Evaluate the Safety & Tolerability of JBZ-001 in Pts With Advanced Solid and Hematological Malignancies
At a glance
Conditions
Where it's being run
2 sites across 2 statesStudy leadership
- Zuzana Jirakova, MD PhD · STUDY_CHAIR · Jabez Biosciences, Inc
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Occurrence of all adverse events28 Days
Evaluation of adverse events
- Maximum tolerated dose (MTD)28 days
MTD will be defined as the maximum dose level at which no more than 1 of 3 participants experience a dose-limiting toxicity (DLT) within the first 33days of multiple dosing.
- Phase II dose (RP2D)28 days
The number and proportion of patients experiencing at least 1 dose-limiting toxicity (DLT) will be used as the primary measure to evaluate the RP2D