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OncoMatch/Clinical Trials/NCT06600698

Safety and Efficacy of AGN-INM176 in Prostate Patients With Rising PSA

Is NCT06600698 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies INM176 for prostate cancer.

Phase 1/2RecruitingMilton S. Hershey Medical CenterNCT06600698Data as of May 2026

Treatment: INM176This Phase I/II open-label trial aims to evaluate the safety and efficacy of the herbal supplement INM176 in patients with a history of prostate cancer or low-risk disease under active surveillance. The study will determine the recommended Phase II dose (RP2D) and assess the efficacy of INM176 in stabilizing or decreasing plasma PSA levels in post-radical prostatectomy (RP) and post-radiation therapy (RT) patients with rising PSA levels.

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Extracted eligibility criteria

Cancer type

Prostate Cancer

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: surgery

Post-radical prostatectomy (RP)

Must have received: radiation therapy

post-radiation therapy (RT)

Must have received: antiandrogen

previous use of antiandrogen therapy

Lab requirements

Blood counts

Hgb ≥ 9.0 g/dL, Platelets ≥ 100 x 10^9/L, absolute neutrophil count ≥ 1.0 x 10^9/L. INR, PT, and PTT within normal institutional limits

Kidney function

Creatinine < 1.5 ULN or creatinine clearance > 50 mL/min/1.73 m2. Chronic kidney disease with calculated GFR <30 mL/min/1.73 m2 using Cockcroft-Gault formula, or measured GFR <30 mL/min/1.73 m2 using a 24-hour urine collection [excluded]

Liver function

Total bilirubin within normal institutional limits. AST(SGOT)/ALT(SGPT) < 2.5 X upper limit of normal (ULN)

Subjects must have normal liver and kidney function at baseline: Total bilirubin within normal institutional limits. AST(SGOT)/ALT(SGPT) < 2.5 X upper limit of normal (ULN). Creatinine < 1.5 ULN or creatinine clearance > 50 mL/min/1.73 m2. Adequate bone marrow function: Hgb ≥ 9.0 g/dL, Platelets ≥ 100 x 10^9/L, absolute neutrophil count of ≥ 1.0 x 10^9/L). International Normalized Ratio (INR), Prothrombin Time (PT), and Partial Thromboplastin Time (PTT) within normal institutional limits.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Penn State Cancer Institute · Hershey, Pennsylvania

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