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NCT Number: NCT05772273

PD-1 Inhibitor, Azacitidine and Low-dose DLI in AML Relapse After Allo-HSCT

This study aims to evaluate the efficacy and safety of PD-1 inhibitor, Azacitidine, and low-dose DLI in AML relapse After allogeneic hematopoietic stem cell transplantation

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, 215006, China

Location status: Recruiting

Location contact

Sheng-Li Xue, M.D.

CONTACT

[email protected]

0086-13328008851

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with a diagnosis of AML relapse after allogeneic hematopoietic stem cell transplantation.
  • Adequate organ function.
  • Be able to understand and sign informed consent.
  • Age 18 to 60 years old.
  • Serum pregnancy test for females of childbearing potential that is negative within one week prior to initiation of first dose of treatment. Female patients of childbearing potential and sexually active males must agree to use a highly effective method of contraception throughout the study and for at least 90 days after the last dose of assigned treatment.
  • ECOG performance status ≤ 1.
  • Known HLA-matched donor without contraindications to donate.
  • Life expectancy > 3 months.

Exclusion criteria

  • Diagnosis of anther malignant disease.
  • Suspected or proven acute or chronic GVHD.
  • Proven central nervous system leukemia.
  • Prior treatment with anti-PD-1, anti-PD-L1, or DLI.
  • HLA loss positive.
  • Known active viral infection with known human immunodeficiency virus (HIV) or viral hepatitis type B (HBV) or C (HCV) or Corona Virus Disease 2019(COVID-19);
  • Uncontrolled systemic fungal, bacterial, or viral infection.
  • Known or suspected hypersensitivity to PD-1 inhibitor or azacytidine.
  • Participation in another clinical study within 3 months.
  • Any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of study procedures.

Treatment and study plan

Azacitidine

Drug

Azacitidine 75 mg/m2 subcutaneously once daily on days 1-7.

donor lymphocyte infusion

Biological

The 4 DLI doses (dose range: ±10%) of sib-matched donor HSCT patients were 1×10^6/kg, 5×10^6/kg, 1×10^7/kg, 5×10^7/kg; The 4 DLI doses (dose range: ±10%) of haploidentical or unrelated donor HSCT patients were 1×10^5/kg, 5×10^5/kg, 1×10^6/kg, 5×10^6/kg.

Camrelizumab

Drug

Camrelizumab 200mg Q2W for sib-matched donor HSCT patients, 100mg Q2W for haploidentical or unrelated donor HSCT patients.

Primary outcomes

  1. Overall response rate (ORR)

    Time frame: ORR assessment is at day 39 (±2).

    The overall response (completed remission, completed remission with incomplete blood count recovery)

Secondary outcomes

  1. Overall Survival (OS)

    Time frame: 2 years

    OS is measured from the time of enrollment to this trial to the date of death from any cause; patients not known to have died at last follow-up are censored on the date they were last known to be alive.

  2. Progression-Free Survival (PFS)

    Time frame: 2 years

    PFS is measured from the time of enrollment to this study to progression or death.

  3. Adverse events

    Time frame: 1 month

    It is evaluated and graded according to CTCAE 5.0.

Study contacts

Contact information is provided by the study sponsor or research team.

Sheng-Li Xue, M.D.

CONTACT

[email protected]

+86 512 6778 1139

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital of Soochow University

Other

Collaborators

  • Jiangsu HengRui Medicine Co., Ltd.

Registry information

Official study title

Efficacy and Safety of PD-1 Inhibitor, Azacitidine and Low-dose DLI in AML Relapse After Allogeneic Hematopoietic Stem Cell Transplantation

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Mar 16, 2023
Registry last updated
Nov 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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