Safety, PK, PD, Dosing, and Efficacy of RLS-0071for the Treatment of Hospitalized Patients With Steroid-Refractory Acute Graft-versus-Host Disease
Condition(s) studied
Investigational drug(s) / intervention(s)
RLS-0071: RLS-0071 will be administered for 7 or 14 days according to the assigned dose group.
Study 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.
Eligibility
Primary outcome measure(s)
- Number of participants with treatment-related adverse events (TEAEs) and Treatment-Emergent Serious Adverse Events (TESAEs) — Day 1 to Day 180
- Overall Response Rate (ORR) of RLS-0071 — Day 1 to Day 28
Trial sites (11)
| Facility | City | Region | Status |
|---|---|---|---|
| Site 1091 | Duarte | California | Active Not Recruiting |
| Site 1343 | Los Angeles | California | Active Not Recruiting |
| Site 1318 | Atlanta | Georgia | Active Not Recruiting |
| Site 1068 | St Louis | Missouri | Active Not Recruiting |
| Site 1100 | Cincinnati | Ohio | Active Not Recruiting |
| Site 1382 | Columbus | Ohio | Active Not Recruiting |
| Site 3242 | Freiburg im Breisgau | Germany | Recruiting |
| Site 3101 | Seville | SE | Recruiting |
| Site 3360 | Madrid | Spain | Recruiting |
| Site 3227 | Salamanca | Spain | Recruiting |
| Site 3101 | Seville | Spain | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06343792 on ClinicalTrials.gov ↗ ← All trials in Spain