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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
Trial Status: active
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.
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
Additional locations may be listed on ClinicalTrials.gov for NCT06343792.