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Safety, PK, PD, Dosing, and Efficacy of RLS-0071for the Treatment of Hospitalized Patients With Steroid-Refractory Acute Graft-versus-Host Disease
Sponsor: ReAlta Life Sciences, Inc.
Summary
This study is a Open Label Prospective Dose-Ranging Escalation and Expansion Trial to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Dosing, and Efficacy of RLS-0071 for the secondary treatment of acute Graft-versus-Host Disease (aGvHD) in hospitalized patients who are steroid-refractory.
Official title: Phase 2 Open Label Prospective Dose-Ranging Clinical Trial With Escalation and Expansion Cohorts to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Dosing, and Efficacy of RLS-0071 for the Treatment of Hospitalized Patients With Steroid-Refractory Acute Graft-versus-Host Disease
Key Details
Gender
All
Age Range
12 Years - Any
Study Type
INTERVENTIONAL
Enrollment
66
Start Date
2024-08-31
Completion Date
2026-12
Last Updated
2025-11-24
Healthy Volunteers
No
Conditions
Interventions
RLS-0071
RLS-0071 will be administered for 7 or 14 days according to the assigned dose group.
Locations (11)
Site 1091
Duarte, California, United States
Site 1343
Los Angeles, California, United States
Site 1318
Atlanta, Georgia, United States
Site 1068
St Louis, Missouri, United States
Site 1100
Cincinnati, Ohio, United States
Site 1382
Columbus, Ohio, United States
Site 3242
Freiburg im Breisgau, Germany
Site 3101
Seville, SE, Spain
Site 3360
Madrid, Spain
Site 3227
Salamanca, Spain
Site 3101
Seville, Spain