Clinical trial · Interventional
PD-1 Inhibitor, Azacitidine and Low-dose DLI in AML Relapse After Allo-HSCT
Efficacy and Safety of PD-1 Inhibitor, Azacitidine and Low-dose DLI in AML Relapse After Allogeneic Hematopoietic Stem Cell Transplantation
NCT05772273CI-TRIAL-00125224recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Acute Myeloid Leukemia | Acute Myeloid Leukemia | CURATED_BROADER | 0.80 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Azacitidine | Drug | Azacitidine | ALIAS |
| Camrelizumab | Drug | Camrelizumab | ALIAS |
| Donor lymphocyte infusion | Biological | Donor Lymphocyte Infusion | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Camrelizumab, Azacitidine and low-dose Donor lymphocyte infusion
- description
- Patients are given azacytidine for 7 days, followed by 4 DLI treatments on Days 10, 17, 24 and 31, with the dose of DLI and Camrelizumab adjusted according to the donor source. Camrelizumab infusions were given 3 hours after completion of the 1st and 3rd DLIs, respectively.
- interventionNames
- Drug: Azacitidine
- Biological: Donor lymphocyte infusion
- Drug: Camrelizumab
Primary outcomes (1)
- measure
- Overall response rate (ORR)
- timeFrame
- ORR assessment is at day 39 (±2).
- description
- The overall response (completed remission, completed remission with incomplete blood count recovery)
Secondary outcomes (3)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: 1. Patients with a diagnosis of AML relapse after allogeneic hematopoietic stem cell transplantation. 2. Adequate organ function. 3. Be able to understand and sign informed consent. 4. Age 18 to 60 years old. 5. 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. 6. ECOG performance status ≤ 1. 7. Known HLA-matched donor without contraindications to donate. 8. Life expectancy \> 3 months. Exclusion Criteria: 1. Diagnosis of anther malignant disease. 2. Suspected or proven acute or chronic GVHD. 3. Proven central nervous system leukemia. 4. Prior treatment with anti-PD-1, anti-PD-L1, or DLI. 5. HLA loss positive. 6. 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); 7. Uncontrolled systemic fungal, bacterial, or viral infection. 8. Known or suspected hypersensitivity to PD-1 inhibitor or azacytidine. 9. Participation in another clinical study within 3 months. 10. Any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of study procedures.
References
Publications (0)
Data not yet available
No reference posted for this study.