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Phase III Clinical Study of VC004 in Patients With Localized Advanced/ Metastatic Solid Tumors
Phase III Clinical Study of VC004 in Patients With Localized Advanced/ Metastatic Solid Tumors

NCT06658353

RecruitingPhase 3

Sponsor: Jiangsu vcare pharmaceutical technology co., LTD

Conditions: Locally Advanced Solid Tumor

Interventions: VC004 Capsules

Countries: China

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 overview

Sex: ALL

Age: 12 Years to

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
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.
Locations (1)
  • Beijing, Beijing Municipality, China