The First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, 215006, China
Location status: Recruiting
NCT Number: NCT05772273
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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Interventional
Not applicable
Suzhou, Jiangsu, 215006, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Azacitidine 75 mg/m2 subcutaneously once daily on days 1-7.
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 200mg Q2W for sib-matched donor HSCT patients, 100mg Q2W for haploidentical or unrelated donor HSCT patients.
Time frame: ORR assessment is at day 39 (±2).
The overall response (completed remission, completed remission with incomplete blood count recovery)
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.
Time frame: 2 years
PFS is measured from the time of enrollment to this study to progression or death.
Time frame: 1 month
It is evaluated and graded according to CTCAE 5.0.
Contact information is provided by the study sponsor or research team.
The First Affiliated Hospital of Soochow University
Other
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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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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