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 range
18 Years
Sex
ALL
See this in plain English?
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 …
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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