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Clinical Trial Summary

The purpose of this study is to evaluate the effect of subcutaneous givosiran (ALN-AS1), compared to placebo, on the rate of porphyria attacks in patients with Acute Hepatic Porphyrias (AHP).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03338816
Study type Interventional
Source Alnylam Pharmaceuticals
Contact
Status Completed
Phase Phase 3
Start date November 16, 2017
Completion date May 31, 2021

See also
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Completed NCT02949830 - A Study to Evaluate Long-term Safety and Clinical Activity of Givosiran (ALN-AS1) in Patient With Acute Intermittent Porphyria (AIP) Phase 1/Phase 2
Completed NCT02943213 - Assessment of Intra-subject Variability in the Bioavailability of Chlorpromazine Hydrochloride Phase 1
Completed NCT02082860 - Phase I Gene Therapy Clinical Trial Using the Vector rAAV2/5-PBGD for the Treatment of Acute Intermittent Porphyria Phase 1
Completed NCT02452372 - A Phase 1 Study of Givosiran (ALN-AS1) in Patients With Acute Intermittent Porphyria (AIP) Phase 1
Completed NCT00418795 - Porphozym in the Treatment of Acute Attacks in AIP Phase 2/Phase 3
Active, not recruiting NCT01617642 - Dental Health, Diet, Inflammation and Biomarkers in Patients With Acute Intermittent Porphyria(AIP)
Completed NCT02076763 - Observational Study of Acute Intermittent Porphyria Patients N/A
Active, not recruiting NCT02935400 - Acute Porphyria Biomarkers for Disease Activity