Diabetes drug shows promise in preventing deadly transplant complication
NCT ID NCT05149365
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether sitagliptin, a diabetes medicine, could prevent acute graft-versus-host disease (GVHD) in 190 adults receiving stem cell transplants from related or unrelated donors. Participants took sitagliptin along with standard GVHD prevention. The main goal was to see if it reduced moderate-to-severe GVHD within 100 days after transplant. The trial also monitored side effects, infections, and survival for one year.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
190 people
The number who actually took part.
- Started
-
Dec 2021
- Finished
-
Jun 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 60 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patient age ≥ 18 to ≤ 60 years 2. Eastern Cooperative Oncology Group (ECOG)score 0-2 points / Karnofsky score ≧80 3. To receive allogeneic hematopoietic stem cell transplantation from related haploid or unrelated donor 4. The pretreatment of modified Bu/Cy+ATG scheme was planned. 5. Patients with malignant hematological diseases indicated by transplantation and in complete remission (CR) state. 6. Expected survival ≥ 3 months 7. Signed written informed consent (Patient must be capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent) 8. Agree to use effective contraception Exclusion Criteria: 1. Prior allogeneic hematopoietic stem cell transplant 2. Allergy/intolerance to Sitagliptin 3. There are contraindications for Sitagliptin use. 4. Moderate or severe renal insufficiency 5. Patients with diabetes mellitus requiring insulin secretagogues and/or insulin 6. Human immunodeficiency virus or active hepatitis C virus or active hepatitis B virus infection 7. Active infection that is difficult to control 8. Vital organ function cannot tolerate transplantation 9. Other malignant tumors outside the blood system, except the following diseases: malignant tumors that have been cured for 3 years without active lesions; Adequate treatment of non-melanoma skin cancer without active foci of malignant amygdala and carcinoma in situ 10. There is evidence that may interfere with the study or make patients at risk of serious complications or medical conditions, including but not limited to serious cardiovascular diseases (such as New York heart association class III or IV heart disease over the past six months of myocardial infarction, unstable type of cardiac arrhythmias) or unstable angina and/or severe lung disease (e.g. History of severe obstructive pulmonary disease and symptomatic bronchospasm) 11. Pregnant or lactating women 12. Any life-threatening medical condition or organ system dysfunction considered by the investigator may endanger the patient's safety by interfering with the absorption or metabolism of sitagliptin or putting study results at unnecessary risk
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Acute-graft-versus-host disease are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
The First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology
Suzhou, Jiangsu, 215000, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can regional data improve bone marrow transplant results for blood cancers?
- Could a frailty score predict which older cancer patients survive intensive care?
- Why COVID-19 hits blood cancer patients harder: scientists map the immune clues
- Can a detailed health check predict who thrives after a stem cell transplant?
- Softer chemo before stem cell transplant aims to cure blood cancers in frail children
- Can a new drug stop the Body's attack after stem cell transplants?