This study is to evaluate the efficacy and safety of JAB-30355 in adult participants with
advanced solid tumors harboring TP53 Y220C mutation.
Additional locations may be listed on ClinicalTrials.gov for NCT06386146.
Locations matching your search criteria
United States
Missouri
Saint Louis
Siteman Cancer Center at Washington UniversityStatus: Active
Name Not Available
Ohio
Cleveland
Case Comprehensive Cancer CenterStatus: Active
Name Not Available
Texas
Houston
M D Anderson Cancer CenterStatus: Active
Name Not Available
This study consists of two parts: Dose Escalation Phase (Phase 1) and Dose Expansion
Phase (Phase 2a). The primary objective of dose escalation is to evaluate the safety and
tolerability, and to determine the MTD of JAB-30355 monotherapy administered in
participants with advanced solid tumors harboring TP53 Y220C mutation. Dose expansion
will further explore JAB-30355's clinical benefit and tolerability in selected dose
levels.
Lead OrganizationJacobio Pharmaceuticals