Clinical Trial

Clinical Study of CVL006 Combination With 9MW2821

Study acronym: CVL006-T1003
Not Yet Recruiting Phase 1/2
View on ClinicalTrials.gov →
Summary
This study is a multi-center, open-label, dose-escalation and dose-optimized phase I/II clinical trial. Objective: To determine the safety, tolerability, PK characteristics and preliminary efficacy data of CVL006 combined with 9MW821 patients with advanced solid tumors.
Trial Details
NCT Number NCT07615660
Lead Sponsor Convalife (Shanghai) Co., Ltd.
Conditions Advanced Solid Tumor
Enrollment 108 participants
Start Date 2026-05-15
Primary Completion 2029-04-30 (estimated)
Study Completion 2029-04-30 (estimated)
Updated on ClinicalTrials.gov 2026-05-29