Ireland
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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
Phase
Phase 3
Started
2025-03-17
Last updated
2026-07-27

Condition(s) studied

Locally Advanced Solid Tumor

Investigational drug(s) / intervention(s)

VC004 Capsules →

VC004 Capsules: VC004 Capsules BID

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

Sex
ALL
Min age
12 Years
Max age
—
Healthy volunteers
No
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)

FacilityCityRegionStatus
Cancer Hospital,Chinese Academy of Medical Sciences and Peking Union Medical College Beijing Beijing Municipality Recruiting
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