Myelodysplastic Syndrome Clinical Trial

Extension Study of RA101495 for Patients With PNH Who Have Completed a Zilucoplan (RA101495) Clinical Study

Summary

The purpose of this study is to enable continued access to zilucoplan (RA101495) for patients with paroxysmal nocturnal hemoglobinuria (PNH) after they complete a zilucoplan clinical study.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Completion of a qualifying Ra Pharmaceuticals sponsored zilucoplan (RA101495) PNH study
Evidence of ongoing clinical benefit in the opinion of the Investigator

Exclusion criteria:

History of meningococcal disease
Current systemic infection or suspicion of active bacterial infection

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

19

Study ID:

NCT03225287

Recruitment Status:

Terminated

Sponsor:

Ra Pharmaceuticals, Inc.

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There are 2 Locations for this study

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Investigative Site 4
Los Angeles California, 90033, United States
Investigative Site 19
Dallas Texas, 75390, United States
Investigative Site 3
Gosford , , Australia
Investigative Site 5
Melbourne , , Australia
Investigative Site 10
Toronto , , Canada
Investigative Site 14
Helsinki , , Finland
Investigative Site 9
Ulm , , Germany
Investigative Site 17
Budapest , , Hungary
Investigative Site 13
Christchurch , , New Zealand
Investigative Site 12
Hamilton , , New Zealand
Investigative Site 6
Leeds , , United Kingdom
Investigative Site 7
London , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

19

Study ID:

NCT03225287

Recruitment Status:

Terminated

Sponsor:


Ra Pharmaceuticals, Inc.

How clear is this clinincal trial information?

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