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Clinical Trials/NCT02222545
NCT02222545
Completed
Phase 2

A Phase 2, Uncontrolled, Three-Stage, Dose-Escalation Cohort Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, Immunogenicity, and Clinical Activity of OMS721 in Adults With Thrombotic Microangiopathies

Omeros Corporation1 site in 1 country58 target enrollmentNovember 2, 2014

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Thrombotic Microangiopathies
Sponsor
Omeros Corporation
Enrollment
58
Locations
1
Primary Endpoint
Number of Participants With HSCT-TMA Who Respond to OMS721
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to assess the safety, efficacy, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of OMS721 in patients with thrombotic microangiopathies (TMA).

Detailed Description

This is a Phase 2, uncontrolled, 3-stage, ascending-dose-escalation study in patients with 1 of 3 forms of TMA: atypical hemolytic uremic syndrome (aHUS), thrombotic thrombocytopenia (TTP), and hematopoietic stem cell transplant - associated TMA (HSCT-associated TMA). In Stage 1 of the study, OMS721 was administered to 3 cohorts, with dose escalation by cohort to identify the optimal dosing regimen. In Stage 2, the dose selected in the first stage was administered to expanded cohorts of patients with distinct etiologies (aHUS alone in 1 cohort and TTP or HSCT-TMA in the other cohort). Patients completing Stage 2 were eligible for continued treatment in Stage 3 if they tolerated OMS721 treatment and derived clinical benefit. Enrollment in the study has been completed.

Registry
clinicaltrials.gov
Start Date
November 2, 2014
End Date
August 11, 2020
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Are at least age 18 at screening (Visit 1)
  • Have a diagnosis of primary aHUS, persistent HSCT-associated TMA or TTP
  • No clinically apparent alternative explanation for thrombocytopenia and anemia

Exclusion Criteria

  • Had eculizumab therapy within three months prior to screening
  • Have STEC-HUS
  • Have a positive direct Coombs test
  • Have an active systemic bacterial or fungal infection requiring antimicrobial therapy (prophylactic antimicrobial therapy administered as standard of care is allowed)

Outcomes

Primary Outcomes

Number of Participants With HSCT-TMA Who Respond to OMS721

Time Frame: Day 1 to up to 2 years following the first dose of OMS721

Response defined as: Improvement in TMA laboratory markers of platelet count and lactate dehydrogenase (LDH) and improvement in clinical status

Assess the Safety and Tolerability of Multiple-dose Administration of OMS721 in Participants With TMA

Time Frame: Day 1 to 37 days after end of treatment, approximately up to 31 weeks.

Incidence of treatment-emergent adverse events (AEs): clinically significant changes in vital signs, ECG, and laboratory tests were reported as AEs.

Secondary Outcomes

  • Participants With HSCT-TMA Treated With OMS721: Freedom From Platelet Transfusion(Study Day -14 to 4 weeks following the last platelet transfusion)
  • Participants With HSCT-TMA Treated With OMS721: Freedom From Red Blood Cell (RBC) Transfusion(Study Day -14 to 4 weeks following the last RBC transfusion)
  • Participants With HSCT-TMA Treated With OMS721: Change From Baseline in Platelet Count(Study Day 1 to Day 97, approximately 13 weeks)
  • Participants With HSCT-TMA Treated With OMS721: 100-day Survival(Study Day of HSCT-TMA diagnosis to 100 days later)
  • Participants With HSCT-TMA: Pharmacokinetics (PK) of Multiple-dose Administration of OMS721(Pre-dose and up to 204 days post-dose)
  • Participants With HSCT-TMA Treated With OMS721: Overall Survival(Study Day of HSCT-TMA diagnosis to up to 2 years following first dose of OMS721)
  • Participants With HSCT-TMA Treated With OMS721: Duration of Response(Study Day 1 to up to 2 years following first dose of OMS721)
  • Participants With HSCT-TMA (ADA)(Pre-dose and up to 204 days post-dose)
  • Participants With HSCT-TMA Treated With OMS721: Change From Baseline in LDH(Study Day 1 to Day 97, approximately 13 weeks)
  • Participants With HSCT-TMA Treated With OMS721: Change From Baseline in Creatine(Study Day 1 to Day 97, approximately 13 weeks)
  • Participants With HSCT-TMA Treated With OMS721: Change From Baseline in Haptoglobin(Study Day 1 to Day 97, approximately 13 weeks)
  • Participants With HSCT-TMA Treated With OMS721: Change From Baseline in Hemoglobin(Study Day 1 to Day 97, approximately 13 weeks)
  • Participants With HSCT-TMA: Pharmacodynamics (PD)(Pre-dose and up to 204 days post-dose)

Study Sites (1)

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