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OncoMatch/Clinical Trials/NCT06245746

UCMSC-Exo for Chemotherapy-induced Myelosuppression in Acute Myeloid Leukemia

Is NCT06245746 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies umbilical cord derived mesenchymal stem cells exosomes (UCMSC-Exo) for acute myeloid leukemia.

Phase 1RecruitingUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyNCT06245746Data as of Jun 2026Location: China

Treatment: umbilical cord derived mesenchymal stem cells exosomes (UCMSC-Exo)The purpose of the study is to explore the safety and efficacy of UCMSC-Exo in consolidation chemotherapy-induced myelosuppression in patients with acute myeloid leukemia after achieving complete remission.

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Extracted eligibility criteria

Treatments studied

Other

umbilical cord derived mesenchymal stem cells exosomes (UCMSC-Exo)

Cancer type

Acute Myeloid Leukemia

Performance status

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

Demographics

Ages ≤ 60

Prior therapy

Must have received: cytarabine or cytarabine-based consolidation therapy (cytarabine) — consolidation

are going to receive consolidation therapy (cytarabine or cytarabine-based combined regimen, the cycle of consolidation therapy is not limited)

Cannot have received: radiation therapy on sternum or pelvis

Previous radiation therapy performed on sternum or pelvis

Cannot have received: immunosuppressants

Continuous usage of immunosuppressants or received organ transplantation in the last 6 months

Cannot have received: clinical trial drugs

Participation in clinical trials of other drugs within 6 weeks before enrollment

Cannot have received: clinical stem cell or exosome research

Previous participation in clinical stem cell or exosome research

Cannot have received: agents inhibiting cell division (hydroxyurea, low-dose cytarabine, methotrexate)

Receive any agent concurrently with UCMSC-Exo infusion which inhibits cell division (hydroxyurea, low-dose cytarabine or methotrexate, etc)

Lab requirements

Kidney function

serum creatinine of at most 1.5 times/upper limit of normal value

Liver function

alanine aminotransferase/aspartate aminotransferase of at most 2.5 times/upper limit of normal value and serum total bilirubin of at most 1.5 times/upper limit of normal value

Cardiac function

ejection fraction of left ventricular of at least 45%

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

Frequently asked questions

Is NCT06245746 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior radiation therapy on sternum or pelvis, immunosuppressants, clinical trial drugs disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 60 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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