A Study of IBI363 in Subjects with Advanced Solid Malignancies

PHASE2RecruitingINTERVENTIONAL
Enrollment

178

Participants

Timeline

Start Date

April 8, 2024

Primary Completion Date

March 1, 2026

Study Completion Date

December 31, 2026

Conditions
MelanomaNon-small Cell Lung CancerColorectal CancerRenal Cell Cancer
Interventions
DRUG

IBI363

IBI363 will be administered as an intravenous (IV) infusion every 2 weeks or every 3 weeks. Subjects will receive study medication until disease progression, toxicity intolerance, withdrawal of consent, the duration of treatment reaches 24 months, or any other reason that requires discontinuation of the study treatment, whichever occurs first.

Trial Locations (9)

33322

RECRUITING

BRCR Medical Center, Plantation

34474

RECRUITING

Ocala Oncology Center, Ocala

48098

RECRUITING

Michigan Hematology & Oncology Consultants - MedOnc Troy, Troy

48126

RECRUITING

Michigan Hematology & Oncology Consultants - MedOnc Dearborn, Dearborn

66205

RECRUITING

University of Kansas Medical Center (KUMC), Fairway

77025

RECRUITING

MD Anderson Cancer Center-University of Texas, Houston

77030

RECRUITING

Oncology Consultants P.A., Houston

94143

RECRUITING

University of California, San Francisco (UCSF), San Francisco

98109

RECRUITING

Fred Hutchinson Cancer Center, Seattle

All Listed Sponsors
lead

Innovent Biologics (Suzhou) Co. Ltd.

INDUSTRY

NCT06281678 - A Study of IBI363 in Subjects with Advanced Solid Malignancies | Biotech Hunter | Biotech Hunter