NCT04669210CompletedPhase 2
PTCy and Ruxolitinib vs PTCy, Tacrolimus and MMF in MUD and Haploidentical HSCT
A Randomized, Multicenter, Open-label Phase II Trial to Compare Prophylaxis of Graft Versus Host Disease With Tacrolimus and Mycophenolate Mofetil Versus Ruxolitinib After Post-transplant Cyclophosphamide
Source: ClinicalTrials.gov · Last updated 4 Jul 2025
Brief summary (registry, in English)
This is multicenter investigator-initiated randomized open-label phase II clinical trial to compare prophylaxis of graft versus host disease treated with tacrolimus and mycophenolate mofetil versus ruxolitinib after post-transplant cyclophosphamide. In total 128 patients will be included in the study. After inclusion into the study and performing of transplantation patients will be randomized in 1:1 proportion in two arms (64 patients per arm): arm A will include patients who will be treated with cyclophosphamide and ruxolitinib for GVHD prophylaxis; arm B will include patients who will be treated with cyclophosphamide, tacrolimus and MMF for GVHD prophylaxis. After the end of the treatment patients will be followed-up during two years.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 128 (actual)
- First submitted
- 26 Nov 2020
- Start date
- 3 Nov 2020
- Primary completion date
- 27 Feb 2023
- Lead sponsor
- St. Petersburg State Pavlov Medical University
- NCT number
- NCT04669210
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 128
- From 3 Nov 2020 to the primary completion date, 27 Feb 2023
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Repeated allogeneic transplantation, regardless of the indications for its implementation;
- Another severe concomitant pathology, which according to the attending physician does not allow the patient to be included in the study;
- Inability to quit smoking for up to 6 months after transplantation;
- Pregnancy or refusal to perform highly effective contraception for 6 months after transplantation.
- Highly effective contraceptive methods include:
- Total abstinence: if it corresponds to the preferred and customary way of life of the patient. Periodic abstinence (for example, calendar, ovulation, symptothermal, postovulation methods) and interrupted sexual intercourse are not considered acceptable methods of contraception;
- Female sterilization (surgical bilateral oophorectomy with or without hysterectomy), total hysterectomy or tubal ligation at least 6 weeks before the start of the therapy being studied. In the case of ovariectomy only, the reproductive status of the woman must be confirmed using a subsequent analysis of hormones;
- Sterilization of the male partner (at least 6 months before screening). For women participating in the study, the sexual partner after a vasectomy should be the only partner;
- Use of oral, injectable or implanted hormonal contraceptive drugs, intrauterine devices or contraceptive systems, or other forms of hormonal contraception with similar efficacy (failure rate less than 1%), for example, hormonal vaginal rings or transdermal hormonal contraceptives.
Other illness
- Uncontrolled bacterial or fungal infection at the time of randomization, determined by the level of CRP\> 70 mg/l with adequate antibacterial or antifungal therapy;
- Rhythm disturbances that persist despite adequate antiarrhythmic therapy: a tachysystolic form of atrial fibrillation, ventricular arrhythmias V gradation according to Laun, AV block of III degree;
- Angina of more than II functional class or unstable angina;
Lab values
- Severe organ failure: creatinine more than 2 ULN; ALT, AST more than 5 ULN; bilirubin more than 1.5 ULN; respiratory failure more than 1 grade;
- Decrease in ejection fraction according to echocardiography less than 40%;
Other
- Source of graft - umbilical cord stem cells;
- Any ex vivo modification of the graft with the exception of separation or washing of red blood cells;
- The presence of more than 5% of clonal tumor cells according to flow cytometry in the presence of morphological remission;
- Diagnosis: acute promyelocytic leukemia;
- Unstable hemodynamics, requiring the introduction of vasopressors;
- Pulmonary pathology with a decrease in FEV1 of less than 60% or pulmonary diffusion capacity of less than 60%;
- Somatic or mental pathology not allowing to sign informed consent.
Who the study is looking for
- Informed consent to participate in the study, signed by the patient;
- Diagnosis: acute lymphoblastic or acute myeloblastic leukemia;
- Morphological remission, defined as less than 5% of blasts by microscopy or flow cytometry with a peripheral leukocyte level of more than 1.500 μL. It is acceptable to include patients without restored platelets or erythrocytes;
- Indications for performing allogeneic hematopoietic stem cell transplantation, determined by the participating center in accordance with local medical practice;
- Unrelated or haploidentical donor;
- Age 18-70 years;
- Functional status according to ECOG scale 0-2 score.
Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| National Hematology Research Center Coordinator of this site? Confirm its status | Moscow | Russia | Unknown status |
| RM Gorbacheva Research Institute Coordinator of this site? Confirm its status | Saint Petersburg | Russia | Unknown status |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.