Clinical Trials in China / NCT06658353
Recruiting
Phase 3
Phase III Clinical Study of VC004 in Patients With Localized Advanced/ Metastatic Solid Tumors
NCT06658353 · tracked via the Priya Life Science China tracker
Condition(s) studied
Locally Advanced Solid Tumor
Study summary
This Study is a single arm, open label, multicenter phase III clinical trial to evaluate the safety and efficacy of VC004 in patients with locally advanced/metastatic solid tumors.
Eligibility
Inclusion Criteria:
* All subjects or legal representatives are willing and able to sign ICF approved by the ethics committee before starting any screening procedures;
* Male or female, age ≥12 years old;
Exclusion Criteria:
* Patients have undergone major surgery within 4 weeks prior to the first dose or are expected to undergo major surgery during the trial (excluding vascular access establishment procedures, biopsy procedures);
* Adverse reactions caused by previous treatment have not recovered to ≤1 grade (evaluated by the investigator);
* Patients had been treated with a strong CYP3A inhibitor or inducer within 7 days prior to the first administration of the study drug.
Primary outcome measure(s)
- Objective response rate(ORR) — 6 months
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Cancer Hospital,Chinese Academy of Medical Sciences and Peking Union Medical College | Beijing | Beijing Municipality | Recruiting |
More Jiangsu vcare pharmaceutical technology co., LTD trials in China
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06658353 on ClinicalTrials.gov ↗ ← All trials in China