drugset / Trial / NCT04959981

A Study of Anti-Cancer Therapies Targeting the MAPK Pathway in Patients With Advanced NSCLC

NCT04959981

Phase 1 Completed 24 enrolled Erasca, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

* To evaluate the safety and tolerability of escalating doses of ERAS-007 or ERAS-601 in combination with other cancer therapies in study participants with advanced non-small cell lung cancer (NSCLC). * To determine the Maximum Tolerated Dose (MTD) and/or Recommended Dose (RD) of ERAS-007 or ERAS-601 administered in combination with other cancer therapies. * To evaluate the antitumor activity of ERAS-007 or ERAS-601 in combination with other cancer therapies. * To evaluate the PK profiles of ERAS-007 or ERAS-601 and other cancer therapies when administered in combination.

Timeline

Start
2021-09-02
Primary completion
2023-04-27
Completion
2023-04-27

Drugs

EvaluationDrugModalityDoseRoute
Subject ERAS-007 Unknown Oral
Subject ERAS-601 Unknown Oral
Subject Osimertinib Small molecule Oral
Subject Sotorasib Small molecule Oral