drugset / Trial / NCT06795412

Phase 1/2 Study of PYX-201 in Combination With Pembrolizumab in Advanced Solid Tumors

NCT06795412

Phase 1/2 Recruiting 220 enrolled Pyxis Oncology, Inc Merck Sharp & Dohme LLC · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objective of this study is to determine the recommended Phase 2 doses (RP2D(s)) and maximum tolerated dose (MTD) of PYX-201 in combination with pembrolizumab for participants with advanced solid tumors.

Timeline

Start
2025-04-15
Primary completion
2027-12-06
Completion
2027-12-06

Drugs

EvaluationDrugModalityDoseRoute
Subject PYX-201 Other / unclassified Intravenous
Background Pembrolizumab Monoclonal antibody Intravenous

Indications