A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Antitumor Activity of INV-9956 in Adult Patients With Advanced Metastatic Castration Resistant Prostate Cancer

This is a Phase 1 and Phase 2 study to evaluate the safety and antitumor activity of INV-9956 in adult patients with advanced metastatic Castration Resistant Prostate Cancer.

Trial Details

NCT ID
NCT06609005
Phase
PHASE1 / PHASE2
Sponsor
Shenzhen Ionova Life Sciences Co., Ltd.
Status
RECRUITING
Cancer Type
Prostate Cancer
Interventions
  • INV-9956
Locations (sample)
  • Scottsdale, Arizona, United States|33.50921,-111.89903
  • Newport Beach, California, United States|33.61891,-117.92895
  • Orange, California, United States|33.78779,-117.85311
  • Houston, Texas, United States|29.76328,-95.36327
  • San Antonio, Texas, United States|29.42412,-98.49363

Key Eligibility Criteria

  • Written informed consent obtained.
  • Male aged ≥ 18 years.
  • Histologically confirmed adenocarcinoma of the prostate.
  • Castration resistant prostate cancer with serum testosterone \<50 ng/dL.

For full eligibility, visit ClinicalTrials.gov.

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