Expanded Access Protocol of Givosiran for Patients With Acute Hepatic Porphyria

NCT04056481 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2024-05-20

No results posted yet for this study

Summary

The purpose of this study is to provide expanded access of givosiran to patients with Acute Hepatic Porphyria (AHP).

Conditions

  • Acute Hepatic Porphyria

Interventions

DRUG

Givosiran

givosiran (ALN-AS1) administered as a subcutaneous (SC) injection

Sponsors & Collaborators

Principal Investigators

  • Medical Director · Alnylam Pharmaceuticals

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04056481 on ClinicalTrials.gov