IBI334 in Subjects With Unresectable, Locally Advanced or Metastatic Solid Tumors - Trial NCT05774873
Access comprehensive clinical trial information for NCT05774873 through Pure Global AI's free database. This Phase 1 trial is sponsored by Innovent Biologics (Suzhou) Co. Ltd. and is currently Not yet recruiting. The study focuses on Solid Tumors. Target enrollment is 128 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
Innovent Biologics (Suzhou) Co. Ltd.
Timeline & Enrollment
Phase 1
Jul 31, 2023
Jun 30, 2026
Primary Outcome
Number of patients with treatment-related adverse events,Percentage of subjects woth Dose-Limitine toxicities(DLTs)
Summary
The primary objective of this study to evaluate the safety and tolerability of IBI334 and
 determine the maximum tolerated dose (MTD) and the recommended Phase 2 Dose (RP2D) of IBI334.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05774873
Non-Device Trial

