Adverum Biotechnologies Begins Patient Enrollment in the ADVANCE Phase 1/2 Clinical Trial for A1AT Deficiency
- Category: DNA RNA and Cells
- Published on Tuesday, 05 December 2017 17:04
- Hits: 645
-- Patients to Receive Single-administration of Gene Therapy Candidate ADVM-043 --
-- Company Expects to Report Preliminary Data in the Second Half of 2018 --
MENLO PARK, CA, USA I December 05, 2017 I Adverum Biotechnologies, Inc. (Nasdaq:ADVM), a leading gene therapy company targeting unmet medical needs in serious rare and ocular diseases, today announced the initiation of patient enrollment in the ADVANCE Phase 1/2 clinical trial of ADVM-043 in patients with alpha-1 antitrypsin (A1AT) deficiency. The ADVANCE clinical trial is designed to evaluate the safety and protein expression following a single administration of ADVM-043, Adverum’s novel gene therapy candidate.
“Our team has been laser-focused on initiating the ADVANCE clinical trial, which is an important milestone that transforms Adverum into a clinical-stage company,” said Amber Salzman, Ph.D., president and chief executive officer of Adverum Biotechnologies. “We are thrilled to collaborate with The Alpha-1 Foundation and gain from their expertise and insight into patient needs. Given their reach and robust Patient Registry, we are grateful for their support in patient recruitment and look forward to working together to develop a new treatment option for patients living with A1AT deficiency.”
“Current approved therapy for A1AT deficiency patients with lung disease is weekly IV plasma-derived protein replacement,” said Henry Moehring, chief executive officer of the Alpha-1 Foundation. “Until new and innovative therapies become available, the weekly infusions unfortunately are lifelong for patients.”
“We are excited to see the ADVANCE clinical trial open for patient enrollment to be able to evaluate ADVM-043 as a novel, single-administration approach for treating A1AT deficiency,” added Jean-Marc Quach, chief executive officer of The Alpha-1 Project (TAP), a wholly-owned subsidiary of the Alpha-1 Foundation.
About the ADVANCE Phase 1/2 Clinical Trial of ADVM-043 for A1AT deficiency
The ADVANCE Phase 1/2 clinical trial is a multi-center, open-label, dose-escalation study of ADVM-043 in patients with A1AT deficiency. The study will include up to 20 patients across up to four dosing cohorts of up to 5 patients each. The first cohort will receive an intravenous (IV) low dose of ADVM-043 of 8E13 total vg (equivalent to approximately 1E12 vg/kg based on an 80-kg patient). The next two cohorts will receive an intermediate IV dose or high IV dose, with the fourth cohort potentially evaluating intrapleural (IP) delivery of ADVM-043.
The study will be conducted at 5 leading centers in the United States. The primary endpoint is safety and tolerability and secondary endpoints include changes in plasma concentrations of both total and M-specific A1AT levels. The Company expects to report preliminary data from this trial in the second half of 2018.
Additional information about this clinical trial can be found at ClinicalTrials.gov under trial identifier number NCT02168686.
ADVM-043 (AAVrh.10-A1AT) is a gene therapy candidate that has the potential to induce stable, long-term A1AT protein following a single administration. In a preclinical proof-of-concept study, ADVM-043 demonstrated robust protein expression above therapeutic levels in mice following either IV or IP administration. In another study in non-human primates, evidence of stable long-term expression of hA1AT mRNA was observed out to one year following IP administration of ADVM-043.
About Alpha-1 Antitrypsin (A1AT) Deficiency
A1AT deficiency is a fairly common orphan disease impacting approximately 100,000 individuals in the United States. It is estimated that 20 million people carry the gene for the disease, which unfortunately can be passed to their children. A1AT deficiency is associated with premature emphysema. The disease is caused by mutations in the SERPINA1 gene, resulting in very low levels of A1AT. The current standard-of-care treatment for patients with A1AT deficiency can be challenging, with weekly IV infusions of an alpha-1 proteinase inhibitor. The current treatment regimen can result in underdosing and lead to worsening lung function.
About Adverum Biotechnologies, Inc.
Adverum is a leading gene therapy company targeting unmet medical needs in serious rare and ocular diseases. Adverum has a robust pipeline that includes product candidates designed to treat rare diseases alpha-1 antitrypsin (A1AT) deficiency and hereditary angioedema (HAE) as well as wet age-related macular degeneration (wAMD). Leveraging a next-generation adeno-associated virus (AAV)-based directed evolution platform, Adverum generates product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum has collaboration agreements with Regeneron Pharmaceuticals to research, develop, and commercialize gene therapy products for ophthalmic diseases and Editas Medicine to explore the delivery of genome editing medicines for the treatment of inherited retinal diseases. Adverum’s core capabilities include clinical development and in-house manufacturing expertise, specifically in process development and assay development. For more information please visit www.adverum.com.
SOURCE: Adverum Biotechnologies