Intratumoral and Systemic Hiltonol® (Poly-ICLC) in Prostate Cancer Patients on Active Surveillance

This is a partially blinded randomized controlled phase II pilot study comparing Poly-ICLC (Hiltonol®) treatment vs no treatment, for prostate cancer participants on active surveillance.

Trial Details

NCT ID
NCT06343077
Phase
PHASE2
Sponsor
Ashutosh Kumar Tewari
Status
RECRUITING
Cancer Type
Prostate Cancer
Interventions
  • Poly-ICLC intramuscular (IM) injection
  • Poly-ICLC, Intertumoral (IT) injection
Locations (sample)
  • New York, New York, United States|40.71427,-74.00597

Key Eligibility Criteria

  • Written informed consent and HIPAA authorization for release of personal health information.
  • NOTE: HIPAA authorization may be included in the informed consent or obtained separately.
  • Age \> 18 years at the time of consent.
  • ECOG Performance Status of 0-1 within 14 days prior to being registered for protocol therapy (Study Procedure Manual).

For full eligibility, visit ClinicalTrials.gov.

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