drugset / Trial / NCT05222802

A Study to Evaluate ERAS-801 in Patients With Recurrent Glioblastoma (THUNDERBBOLT-1)

NCT05222802

Phase 1 Active not recruiting 52 enrolled Katmai Pharmaceuticals Inc. Erasca, Inc. · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

* To evaluate the safety and tolerability of escalating doses of ERAS-801 in study participants with recurrent glioblastoma multiforme (GBM). * To determine the Maximum Tolerated Dose (MTD) and/or Recommended Dose (RD) of ERAS-801. * To evaluate the antitumor activity of ERAS-801. * To evaluate the PK profile of ERAS-801.

Timeline

Start
2022-02-25
Primary completion
2025-08-31
Completion
2025-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ERAS-801 Small molecule Oral

Indications