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NCT06343077
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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