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RECRUITING
NCT06343792
PHASE2

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.

View on ClinicalTrials.gov

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

Interventions

DRUG

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