NL-OMON43030
Not yet recruiting
Phase 3
Prospective Follow-up Study for Patients who Completed Study ALX0681-C301 (HERCULES) to Evaluate Long-term Safety and Efficacy of Caplacizumab (Post-HERCULES) - Post-HERCULES
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Thrombotic Thrombocytopenic Purpura
- Sponsor
- Ablynx NV
- Enrollment
- 8
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Completed the Final (28 day) FU visit in Study ALX0681\-C301\.
- •2\. Is \>\= 18 years of age at the time of signing the informed consent form (ICF).
- •3\. Provided informed consent prior to initiation of any study specific activity/procedure.
Exclusion Criteria
- •1\. Not being able/willing to comply with the study protocol procedures.
- •2\. Currently enrolled in a clinical study with another investigational drug or device.
Outcomes
Primary Outcomes
Not specified
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