Safety and Efficacy Study of OMS721 in Patients With Thrombotic Microangiopathies

NCT02222545 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2024-08-28

Study results available
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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).

Conditions

  • Thrombotic Microangiopathies

Interventions

BIOLOGICAL

OMS721

Sponsors & Collaborators

  • Omeros Corporation

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-02
Primary Completion
2020-01-30
Completion
2020-08-11

Countries

  • United States
  • Belgium
  • Bulgaria
  • Hong Kong
  • Italy
  • Lithuania
  • Malaysia
  • New Zealand
  • Poland
  • Singapore
  • Taiwan
  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02222545 on ClinicalTrials.gov