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NCT05509933

Budesonide Prophylaxis for Engraftment Syndrome After Hematopoietic Cell Transplantation

Recruiting now Phase 3 Last updated 29 April 2025
What this trial tests

Phase 3 trial testing Budesonide in Engraftment Syndrome in 110 participants. Currently enrolling.

Timeline
9 November 2022
Primary endpoint
30 December 2026
30 December 2026

Quick facts

Lead sponsorHenry Ford Health System
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment110
Start date9 November 2022
Primary completion30 December 2026
Estimated completion30 December 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Henry Ford Health System — full company profile →

Who can join

Adults 18 to 80, any sex, with Engraftment Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine if budesonide prophylaxis starting day 5 after transplant reduces engraftment fever in autologous and allogeneic stem cell transplant recipients.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The Development of New Agents for Post-Hematopoietic Stem Cell Transplantation Non-Infectious Complications in Children.
    Ilan U, Brivio E, Algeri M, Balduzzi A, et al · · 2023 · cited 2× · PMID 36983151 · DOI 10.3390/jcm12062149

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Other trials of Budesonide

Trials testing the same drug.

Other Henry Ford Health System trials

Trials by the same sponsor.

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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/NCT05509933.

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