A Study of IBI3004 in Subjects With Unresectable, Locally Advanced or Metastatic Solid Tumors

PHASE1/PHASE2RecruitingINTERVENTIONAL
Enrollment

106

Participants

Timeline

Start Date

August 19, 2024

Primary Completion Date

August 1, 2025

Study Completion Date

May 1, 2026

Conditions
Solid Tumor
Interventions
DRUG

IBI3004

IBI3004 will be administered. The Dose Limiting Toxicity (DLT) will be observed in the first treatment cycle. After completion of the DLT observation period, subjects will continue to receive IBI3004 until death, disease progression, intolerable toxicity, start of a new anticancer treatment, withdrawal of consent for study participation, end of the study, or for a maximum of 24 months, whichever occurs first.

Trial Locations (5)

2170

TERMINATED

Liverpool Hospital, Sydney

TERMINATED

Westmead Hospital, Sydney

2770

TERMINATED

Scientia Clinical Research Ltd, Randwick

210024

RECRUITING

Jiang Su Province Hospital, Nanjing

310009

RECRUITING

The Second Affiliated Hospital Zhejiang University School of Medicine, Hangzhou

All Listed Sponsors
lead

Innovent Biologics (Suzhou) Co. Ltd.

INDUSTRY