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Clinical Trial Summary

Evaluate safety and tolerability, while establishing the recommended dose of the investigational drug combination of adagrasib and olaparib that can be given to participants with advanced solid tumor(s) with a KRAS G12C and/or KEAP1 mutation.


Clinical Trial Description

Primary Objectives - To evaluate the safety and tolerability of adagrasib in combination with olaparib in participants with KRAS G12C mutant advanced solid tumors. - To establish the maximum tolerated dose and/or recommended phase 2 dose (MTD/RP2D) of the combination in participants with KRAS G12C mutant advanced solid tumors. Secondary Objectives - To assess the preliminary antitumor activity of the combination of adagrasib in combination with olaparib using objective response rate (ORR) = RECISTv1.1 complete response plus partial response (CR+PR). Exploratory Objectives - To assess predictive biomarkers of response and resistance to the combination of adagrasib with olaparib. - To evaluate the pharmacodynamic profile of the combination of adagrasib and olaparib in participants with KRAS G12C mutant advanced solid tumors. - To assess potential mechanisms of response and resistance by comparing serially collected circulating tumor DNA (ctDNA) samples and biopsies in responders and non-responders. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06130254
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Timothy Yap, MD
Phone 713-563-1784
Email TYap@mdanderson.org
Status Recruiting
Phase Phase 1
Start date January 30, 2024
Completion date August 25, 2030

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