drugset / Trial / NCT06797336

A Study of PT0253 in Participants With KRAS G12D Mutated Advanced Solid Tumors

NCT06797336 ↗

Phase 1 Recruiting 115 enrolled PAQ Therapeutics, Inc.
RandomizedSequentialOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the safety and tolerability, determine the maximally tolerated dose (MTD) and/or recommended Phase 2 dose(s) (RP2D) of PT0253 in adult participants with Kirsten rat sarcoma viral oncogene homolog (KRAS) G12D mutated advanced solid tumors as monotherapy.

Timeline

Start
2024-12-19
Primary completion
2026-12-15
Completion
2027-06-16

Drugs

EvaluationDrugModalityDoseRoute
Subject PT0253 Unknown — Intravenous

Indications