Amyloidosis, Hereditary Clinical Trial
Official title:
Expanded Access Program for Inotersen (ISIS 420915) in Patients With Hereditary Transthyretin Amyloidosis (hATTR)
The purpose of this program is to provide expanded access to Inotersen for up to 100 Patients with Hereditary Transthyretin Amyloidosis (hTTR).
The Program is intended to provided expanded access to Inotersen for eligible patients with hATTR who have limited or no available treatment options. ;
Status | Clinical Trial | Phase | |
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Not yet recruiting |
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Southeastern ATTR Amyloidosis Consortium: SEATTRAC Family Registry
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Recruiting |
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Prospective Evaluation of NfL as a Biomarker in ATTRv
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Recruiting |
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Completed |
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APOLLO: The Study of an Investigational Drug, Patisiran (ALN-TTR02), for the Treatment of Transthyretin (TTR)-Mediated Amyloidosis
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Phase 3 | |
Active, not recruiting |
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Phase 3 | |
Completed |
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ENDEAVOUR: Phase 3 Multicenter Study of Revusiran (ALN-TTRSC) in Patients With Transthyretin (TTR) Mediated Familial Amyloidotic Cardiomyopathy (FAC)
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Phase 3 | |
Recruiting |
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Myocardial Effects in Patients With ATTRv With Polyneuropathy Treated With Patisiran or Vutrisiran
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Approved for marketing |
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Expanded Access Protocol of Patisiran for Patients With Hereditary ATTR Amyloidosis (hATTR)
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