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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 15 August 2022
Main ID:  NCT03030183
Date of registration: 20/01/2017
Prospective Registration: Yes
Primary sponsor: Ra Pharmaceuticals
Public title: Phase 2 Safety and Efficacy Study of Zilucoplan (RA101495) to Treat PNH Patients Who Have an Inadequate Response to Eculizumab
Scientific title: A Phase 2 Multicenter, Open-Label, Uncontrolled Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of RA101495 in Subjects With Paroxysmal Nocturnal Hemoglobinuria Who Have an Inadequate Response to Eculizumab
Date of first enrolment: April 17, 2017
Target sample size: 3
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT03030183
Study type:  Interventional
Study design:  Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).  
Phase:  Phase 2
Countries of recruitment
United States
Contacts
Name:     Dr. Anita Hill
Address: 
Telephone:
Email:
Affiliation:  St James' Institute of Oncology
Key inclusion & exclusion criteria
Health Condition(s) or Problem(s) studied
Intervention(s)
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Secondary Sponsor(s)
Ethics review
Results
Results available: Yes
Date Posted: 26/02/2020
Date Completed:
URL: https://clinicaltrials.gov/ct2/show/results/NCT03030183
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