OncoMatch/Clinical Trials/NCT06526338
Adjuvant IP-001 Treatment for HCC Patients Following Surgical Resection and Ablation or Ablation Alone
Is NCT06526338 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies 1.0% IP-001 for for hepatocellular carcinoma.
Treatment: 1.0% IP-001 for — The purpose of this study is to evaluate the safety and efficacy of a single injection of IP-001 as adjuvant therapy after local ablation or surgical resection and ablation in patients with hepatocellular carcinoma (HCC).
Check if I qualifyExtracted eligibility criteria
Cancer type
Hepatocellular Carcinoma
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Cannot have received: local therapy to liver (ablation other than radiofrequency or microwave ablation, i.e., alcohol ablation, transcatheter chemoembolization, transcatheter embolization, hepatic arterial infusion, local radiation/Stereotactic Body Radiation Therapy or radioembolization)
Has received local therapy to liver, ablation other than radiofrequency or microwave ablation (i.e., alcohol ablation, transcatheter chemoembolization, transcatheter embolization, hepatic arterial infusion, local radiation/Stereotactic Body Radiation Therapy or radioembolization) less than 3 months prior to treatment
Cannot have received: antineoplastic systemic chemotherapy or biological therapy
Antineoplastic systemic chemotherapy or biological therapy less than 21 days from treatment or 5 drug elimination half-lives, whichever is shorter prior to randomization
Cannot have received: immunotherapy
Exception: immunotherapy specified in this protocol
Immunotherapy not specified in this protocol less than 21 days from treatment or 5 drug elimination half-lives, whichever is shorter prior to randomization
Cannot have received: systemic glucocorticoids
Exception: inhaled or topical steroids allowed; systemic steroids at doses ≤10 mg/day prednisone or equivalent allowed; steroids may be used for premedication prior to imaging
Systemic glucocorticoids for any purpose other than to modulate symptoms from an adverse event (AE) that is suspected to have an immunologic etiology. Inhaled or topical steroids are allowed, and systemic steroids at doses ≤10 mg/day prednisone or equivalent are allowed. Exception: steroids may be used for premedication prior to imaging
Lab requirements
Blood counts
Kidney function
Liver function
Has adequate organ function as specified in the Adequate Organ Function Laboratory Values Table. Specimens must be collected within 14 days prior to Day 1.
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of Louisville · Louisville, Kentucky
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