Last reviewed · How we verify

NCT06334367

Prophylaxis of Graft-versus-host Disease With Anti-CD25 Antibody in Patients Underwent HSCT

Status unknown Phase 2 Last updated 28 March 2024
What this trial tests

Phase 2 trial testing CD25 treatment in GVHD in 40 participants. Status unknown.

Timeline
26 March 2024
Primary endpoint
26 March 2026
26 March 2026

Quick facts

Lead sponsorWang Xin
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment40
Start date26 March 2024
Primary completion26 March 2026
Estimated completion26 March 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Wang Xin — full company profile →

Who can join

Adults 18 to 60, any sex, with GVHD. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The risk of Graft-versus-host Disease(GVHD) is significantly associated with the mortality rate of patients undergoing allogeneic hematopoietic stem cell transplantation. The occurrence of GVHD increases the hospitalization rate and economic burden of patients. In order to explore better methods for controlling GVHD, we designed a clinical trial using CD25 monoclonal antibody for GVHD prevention. Our previous studies have shown that reduced-dose anti-thymocyte globulin(ATG) in the conditioning regimen can achieve the same effect as full-dose ATG. Here, we try to explore the preventive effect of CD25 antibody on acute and chronic GHVD under low-dose ATG pretreatment condition.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for GVHD

Currently open trials in the same condition.

Other Wang Xin trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06334367.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing