This study is to evaluate the safety and tolerability of JAB-21822 monotherapy and
combination therapy in adult participants with advanced solid tumors harboring KRAS G12C
mutation.
Additional locations may be listed on ClinicalTrials.gov for NCT05002270.
See trial information on ClinicalTrials.gov for a list of participating sites.
The primary objective of this study is to evaluate the safety and tolerability of
JAB-21822 monotherapy to determine the MTD and PR2D during Dose Escalation phase; then to
evaluate preliminary antitumor activity when JAB-21822 administered alone and combination
with cetuximab during Dose Expansion phase in adult participants with advanced solid
tumors harboring KRAS G12C mutation.
Lead OrganizationJacobio Pharmaceuticals