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Monoclonal Antibodies
OMS721 for Hemolytic Uremic Syndrome (aHUS Trial)
Phase 3
Recruiting
Research Sponsored by Omeros Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 771 days post-dose
Awards & highlights
No Placebo-Only Group
Pivotal Trial
Summary
The purpose of this study is to evaluate the platelet count change from baseline and safety of OMS721 in adults and adolescents with atypical hemolytic uremic syndrome (aHUS). The study will also evaluate pharmacokinetics (PK), pharmacodynamics (PD), and anti-drug antibody response (ADA).
Eligible Conditions
- Hemolytic Uremic Syndrome
- Thrombotic Microangiopathy
- Atypical Hemolytic Uremic Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 771 days post-dose
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~771 days post-dose
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
The effect of OMS721 as measured by platelet count change from baseline
Secondary study objectives
Change from baseline in haptoglobin
Change from baseline in serum LDH
Change from baseline in serum creatinine
+7 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
1Treatment groups
Experimental Treatment
Group I: OMS721Experimental Treatment1 Intervention
Administration of OMS721
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Narsoplimab
Not yet FDA approved
Find a Location
Who is running the clinical trial?
Omeros CorporationLead Sponsor
28 Previous Clinical Trials
3,723 Total Patients Enrolled
Eckhard Leifke, M.D.Study DirectorOmeros Corporation
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