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OncoMatch/Clinical Trials/NCT06944457

Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetics of MPD-1 in Patients With Advanced Solid Tumor

Is NCT06944457 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies MPD-1 for cancer.

Phase 1RecruitingPharosgen Co.,LtdNCT06944457Data as of May 2026

Treatment: MPD-1A Phase I, Open-label, Single-center, Dose-escalation and Dose-finding Clinical trial to evaluate the safety, tolerability and pharmacokinetics of MPD-1 in patients with advanced solid tumor

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Biomarker criteria

Required: KRAS mutation

Required: PTEN loss

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: all available existing standard therapy

has used all available existing standard therapy but tumor progression is confirmed and further treatment tool is absent, or patient showing resistant or inadequate to standard therapy

Cannot have received: anthracycline

Patients without the history of administration of anthracycline drugs and/or anthracene

Lab requirements

Blood counts

WBC ≥ 3,500/mm3; ANC ≥ 1,500/mm3 (without CSF within 2 weeks prior to C1D1); platelets ≥ 100,000/mm3 (without transfusion within 2 weeks prior to C1D1); hemoglobin ≥ 10 g/dL (without transfusion within 2 weeks prior to C1D1); INR ≤ 1.5x ULN

Kidney function

serum creatinine ≤ 1.5x ULN

Liver function

total bilirubin ≤ 1.5x ULN (Gilbert syndrome exception); AST, ALT ≤ 2.5x ULN (≤ 5x ULN with liver metastasis); albumin ≥ 2.5 g/dL

Cardiac function

LVEF ≥ 50%, no congestive heart failure NYHA class II or higher, no myocarditis, myocardial infarction or unstable angina within 24 weeks before C1D1, no uncontrolled cardiac dysrhythmia, no coronary artery disease

appropriate hematologic, kidney, and liver function confirmed by the following laboratory test... LVEF <50%, congestive heart failure with NYHA class II or higher, history of myocarditis, myocardial infarction or unstable angina within 24 weeks before C1D1, uncontrolled cardiac dysrhythmia by appropriate medication, coronary artery disease, etc.

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

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