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OncoMatch/Clinical Trials/NCT06380660

Study of ACE-86225106 to Treat Patients With Advanced Solid Tumors

Is NCT06380660 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies ACE-86225106 tablet for solid tumor, adult.

Phase 1/2RecruitingAcerand Therapeutics (Shanghai) LimitedNCT06380660Data as of May 2026

Treatment: ACE-86225106 tabletThe purpose of this study is to determine if the experimental treatment with poly-ADP ribose polymerase (PARP) inhibitor, ACE-86225106 is safe, tolerable and has anti-cancer activity in adult patients with advanced solid tumors.

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Ovarian Cancer

Breast Carcinoma

Prostate Cancer

Disease stage

Metastatic disease required

Advanced solid tumors, difficult to treat or intolerant to standard treatment, suitable for investigational treatment; Has measurable disease per RECIST 1.1, castration-resistant prostate cancer (CRPC) patients can be assessed according to PCWG3

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: anti-cancer drugs

Exception: protocol-defined wash-out period

Receiving any anti-cancer drugs, major surgery, extensive radiation therapy, or local radiation therapy within protocol-defined wash-out period

Lab requirements

Blood counts

adequate bone marrow function

Kidney function

adequate organ function

Liver function

adequate organ function

Adequate organ function and bone marrow function

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

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