Safety Dose Finding Study of ADVM-043 Gene Therapy to Treat Alpha-1 Antitrypsin (A1AT) Deficiency (NCT02168686) | Clinical Trial Compass
CompletedPhase 1/2
Safety Dose Finding Study of ADVM-043 Gene Therapy to Treat Alpha-1 Antitrypsin (A1AT) Deficiency
United States6 participantsStarted 2017-11-28
Plain-language summary
The ADVANCE study is being conducted by Adverum Biotechnologies, Inc. as an open-label, multicenter, dose-escalation study in order to assess the safety and protein expression of ADVM-043 following a single intravenous or intrapleural administration.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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 …
What they're measuring
1
Treatment-emergent Adverse Events Related to ADVM-043
Timeframe: From ADVM-043 infusion through End-of-Study visit at 52 weeks
2
Abnormal Changes in Clinical Laboratory Parameters
Timeframe: From ADVM-043 infusion through End-of-Study visit at 52 weeks