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Safety Dose Finding Study of ADVM-043 Gene Therapy to Treat Alpha-1 Antitrypsin (A1AT) Deficiency

Plain-language summary

This study evaluates a gene therapy (ADVM-043) in patients with Alpha-1 Antitrypsin (A1AT) Deficiency (an inherited disease caused by mutations in the SERPINA1 gene). It included patients over 18 with a ZZ or Z Null genotype. It was a Phase 1/Phase 2 study and has been completed.

The summary above is a plain-language rendering of the official record. The original English title is shown for reference.

Trial details

Phase
PHASE1/PHASE2
Status
Completed
Sponsor
Adverum Biotechnologies, Inc.
Intervention
ADVM-043 (AAVrh.10halpha1AT, AAVrh.10hA1AT)
Start date
11/28/2017
Estimated completion
8/29/2019
Countries
United States

Related genes

Locations

  • Gainesville, United States
  • Charleston, United States

Eligibility criteria

Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.

Key Inclusion Criteria:

* Capable of providing informed consent
* Alpha1AT genotype of ZZ or Z Null
* Males and females 18 years and older
* Ongoing treatment with A1AT augmentation is not required, however any subject receiving A1AT augmentation therapy must be willing to washout. Washout is defined as at least 8 weeks between last augmentation therapy and pre-treatment plasma A1AT level
* Willing to remain off PAT for at least 3 months following treatment
* Body mass index 18 to 35 kg/m2
* Fertile men and women of childbearing potential must agree to use barrier contraception for 3 months after treatment

Key Exclusion Criteria:

* FEV1 \<35 percent of predicted value at the Screening visit
* Receiving systemic corticosteroids or other immunosuppressive medications
* Immunodeficiency disease or evidence of active infection of any type, including human immunodeficiency virus
* Abnormal liver function tests
* Organ transplant recipient or awaiting transplantation
* Participation in another current or previous gene transfer study
* AAVrh.10 neutralizing antibody titer ≥ 1:5
* Female who is pregnant or lactating
* History of alcohol or drug abuse within the past 5 years
* Any history of allergies that may prohibit study-specific investigations
* Receiving an investigational medicinal product or participating in another investigational study within 3 months prior to consent
* Cigarette smoking, or any other tobacco use, e-cigarettes or other recreational inhalant within 1 year of the Screening Visit
This is not medical advice. Consult your specialist.
View the official record on ClinicalTrials.gov →