Clinical Trial

Clinical Study of CVL006 Injection in Advanced Solid Tumors

Not Yet Recruiting Phase 1
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Summary
Evaluate the safety and tolerability of CVL006 monotherapy in patients with advanced solid tumors; Observe the dose limiting toxicity (DLT) of CVL006 monotherapy in patients with advanced solid tumors, evaluate the maximum tolerated dose (MTD), and recommend the dosage for phase II clinical trials (RP2D).
Trial Details
NCT Number NCT06621615
Lead Sponsor Convalife (Shanghai) Co., Ltd.
Conditions Advanced Solid Tumor
Enrollment 120 participants
Start Date 2024-11-20
Primary Completion 2028-05-20 (estimated)
Study Completion 2028-11-20 (estimated)
Updated on ClinicalTrials.gov 2024-10-01