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Clinical Trials in the USA / NCT06343792
Recruiting Phase 2

Safety, PK, PD, Dosing, and Efficacy of RLS-0071for the Treatment of Hospitalized Patients With Steroid-Refractory Acute Graft-versus-Host Disease

NCT06343792 · tracked via the Priya Life Science USA tracker
Sponsor
ReAlta Life Sciences, Inc.
Phase
Phase 2
Started
2024-08-31
Last updated
2025-11-24

Condition(s) studied

Steroid Refractory GVHD

Investigational drug(s) / intervention(s)

RLS-0071

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

Sex
ALL
Min age
12 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Male or female adults or adolescents (\>12 years old). * Hospitalized with steroid-refractory aGvHD (grade II-IV) after allo-HSCT * Anticipated hospital length-of-stay of at least 1 week from the time of RLS-0071 initiation. * No plans to add additional GvHD treatment medications or to add, dose-adjust, or discontinue GvHD prophylactic medications during the 7-days of RLS-0071 treatment. * Neutrophil recovery following the stem-cell transplantation, defined as blood neutrophil count \>500/mL for at least 3 consecutive measurements and not supported by growth factor supplementation * Weight ≥40 kg and ≤ 140 kg at screening. Exclusion Criteria: * Has received more than 1 allo-HSCT * Current, previous, or planned use of any systemic treatment in addition to or other than corticosteroids or ruxolitinib for aGvHD * Previous failure of ruxolitinib treatment * Uncontrolled GI infection * Endoscopic and biopsy testing (if performed) that definitively rules out lower GI aGvHD * Chronic GvHD * Participants with evidence of relapsed primary disease, or participants who have been treated for relapse after the allo-HSCT was performed. * Unresolved toxicity or complications (other than aGvHD) due to the allo-HSCT * Any corticosteroid therapy for indications other than aGvHD at doses of methylprednisolone or equivalent \>1 mg/kg per day within 7 days of enrollment. * Severe organ dysfunction unrelated to underlying aGvHD * Known hypersensitivity, allergy, or anaphylactic reaction to polyethylene glycol (PEG) * Significant liver disease that is unrelated to GvHD * Severe kidney disease * Currently breast feeding. * Known pregnancy, a positive pregnancy test at screening, or lactation for WOCBP. * Active hepatitis B virus (HBV) or hepatitis C virus infection that requires treatment or human immunodeficiency virus (HIV)-1 or HIV-2. * Active sepsis

Primary outcome measure(s)

Trial sites (11)

FacilityCityRegionStatus
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

More ReAlta Life Sciences, Inc. trials in the USA

Official registry record

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 the USA