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Clinical Trial Summary

This is a Phase 1 study of BBP-398, a SHP2 inhibitor, in combination with sotorasib, a KRAS-G12C inhibitor (KRAS-G12Ci), in patients with a KRAS-G12C mutation. The study involves 2 parts: Phase 1a Dose Escalation and Phase 1b Dose Expansion/Optimization.


Clinical Trial Description

The primary objectives for Phase 1a Dose Escalation are to evaluate safety and tolerability, and recommend a phase 1b dose (RP1bD) of the combination. The primary objectives for Phase 1b Dose Expansion/Optimization are to evaluate safety and tolerability, and the antitumor activity (defined by the ORR assessed by the investigator according to RECIST v1.1) of BBP-398 when used in combination with sotorasib across two dose regimens in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with a KRAS-G12C mutation and who are KRAS-G12Ci naïve, and recommend a phase 2 dose (RP2D) of the combination. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05480865
Study type Interventional
Source Navire Pharma Inc., a BridgeBio company
Contact Navire Clinical Operations
Phone 650-391-9740
Email NAV1003ct.gov@bridgebio.com
Status Recruiting
Phase Phase 1
Start date July 6, 2022
Completion date June 2025

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