Arrowhead Files for Regulatory Permission to Begin Phase 1 Trial of RNAi Therapeutic ARC-AAT
Pending approval, Arrowhead intends to proceed with a double blind,
placebo-controlled dose escalation, Phase 1 study to determine the
safety, tolerability, pharmacokinetics and effect on circulating alpha-1
antitrypsin levels of ARC-AAT in healthy volunteers and patients with
alpha-1 antitrypsin deficiency. The study is planned to start in
The application was submitted to an ethics committee in compliance with
the Clinical Trial Notification process of the
About ARC-AAT
Arrowhead has developed ARC-AAT for the treatment of liver disease associated with Alpha-1 Antitrypsin Deficiency (AATD), a rare genetic disease that severely damages the liver and lungs of affected individuals. ARC-AAT employs a novel unlocked nucleobase analog (UNA) containing RNAi trigger molecule designed for systemic delivery using the Dynamic Polyconjugate delivery system. ARC-AAT is highly effective at knocking down the Alpha-1 antitrypsin (AAT) gene transcript and reducing the hepatic production of the mutant AAT (Z-AAT) protein. Reduction of liver production of the inflammatory Z-AAT protein, which has been clearly defined as the cause of progressive liver disease in AATD patients, is important as it is expected to halt the progression of liver disease and potentially allow fibrotic tissue repair.
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