RLS-0071
DrugRLS-0071 will be administered for 7 or 14 days according to the assigned dose group.
NCT Number: NCT06343792
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.
Interested in participating?
Request Info12 year and older
All sexes
Interventional
Phase 2
Site 3242, Freiburg im Breisgau, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
RLS-0071 will be administered for 7 or 14 days according to the assigned dose group.
Time frame: Day 1 to Day 180
Time frame: Day 1 to Day 28
Time frame: Days 7, 14, 28, 56, and 180
Time frame: Days 7, 14, 28, 56, and 180
Time frame: Day 1 - Day 180
Time frame: Days 7, 14, 28, 56, and 180
Time frame: Days 7, 14, 28, 56, and 180
Time frame: Day 0 - Days 7, 14, 28, 56, and 180.
Time frame: Day 1 - Day 180
Time frame: Day 1 - Day 180
Time frame: Day 1 - Day 180
Contact information is provided by the study sponsor or research team.
ReAlta Life Sciences, Inc.
Industry
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
Acronym: AURORA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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