OncoMatch/Clinical Trials/NCT07337525
A First in Human Study of PLT012 in Participants With Solid Tumor Cancers
Is NCT07337525 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies PLT012 for advanced malignant solid tumor.
Treatment: PLT012 — The goal of this clinical trial is to learn about what doses of PLT012 are safe to use in adults with advanced cancers in solid tumors. It will also learn about how effective different doses of PLT012 are in treating cancer. The main questions it aims to answer are: What adverse events and toxicities (harmful side effects) are associated with different doses of PLT012? What are the blood levels of PLT012 in your body at different timepoints? What effect does PLT012 have on reducing tumor size and/or preventing the worsening of cancer? All participants will receive PLT012 and none will receive placebo (a look-alike substance that contains no drug). Participants will receive PLT012 by intravenous infusion once every 3 weeks. Treatment with PLT012 can continue until the participant's disease worsens or they cannot tolerate treatment. For the first 12 weeks, visits to the clinic will be more frequent (from 1 to 5 times over a 3-week period). After the first 12 weeks, visits will be reduced to once every 3 weeks.
Check if I qualifyExtracted eligibility criteria
Cancer type
Tumor Agnostic
Performance status
ECOG 0–1(Restricted strenuous activity)
Lab requirements
Blood counts
Adequate organ function as defined by protocol-specified laboratory values
Kidney function
Adequate organ function as defined by protocol-specified laboratory values
Liver function
Child-Pugh score of Class A (for hepatocellular carcinoma only)
Adequate organ function as defined by protocol-specified laboratory values; Child-Pugh score of Class A (for hepatocellular carcinoma only)
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- NEXT Dallas · Dallas, Texas
- NEXT Houston · Houston, Texas
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