Long Term Safety of Alpha1-Proteinase Inhibitor in Subjects With Alpha1 Antitrypsin Deficiency

Enrolling by invitation · Phase 3

Conditions studied: Pulmonary Emphysema in Alpha-1 Antitrypsin Deficiency

In brief

This is a 2-year open-label, multicenter extension of the double-blind, placebo-controlled GTi1201 study. The purpose of this study is to obtain an additional 2 years of safety data for intravenously administered Alpha1-MP 60 mg/kg/week in subjects with alpha1-antitrypsin deficiency (AATD).

Key facts

Study ID

NCT02796937

Run by

Grifols Therapeutics LLC

People needed

290

Starts

2016-07-01

Expected to finish

2029-02-01

Last updated by the study team

2026-06-23

Who can join

Age: 20 and older, up to 72. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Has completed participation in Study GTi1201 (ie, completed Week 156 and Week 160/End-of-Study Visit) OR has experienced a decline in FEV1 at the annualized rate of ≥134.4 mL/year at or after the Week 104 Visit in GTi1201.
• Is willing and able to provide informed consent

You may not qualify if…

• Is unable to physically or mentally undergo a CT scan (eg, unable to fit inside the CT scanner, claustrophobic).
• Has severe concomitant disease including, but not limited to, congestive heart failure and liver cirrhosis.
• Has primary and/or secondary (metastatic disease) pulmonary malignancy or other current malignancy with <1 year predicted overall survival.
• Has a metal object (newly received since starting GTi1201) that might interfere with chest CT quality and quantification. Metal objects include, but are not limited to, cardiac pacemaker, defibrillator, metal prosthetic heart valve, metal projectile, metal weapon fragments, or metal shoulder prosthesis.
• Is a female who is pregnant, breastfeeding or, if of child-bearing potential, unwilling to practice a highly effective method of contraception (oral, injectable, or implanted hormonal methods of contraception; placement of an intrauterine device or intrauterine system; condom or occlusive cap with spermicidal foam/gel/film/cream/suppository; male sterilization; or abstinence) throughout the study.
• Has clinical signs and symptoms of viral infection requiring virus safety testing at the Week 160/End-of-Study Visit or Early Discontinuation Visit in Study GTi1201, and the virus safety test results are indicative of acute or chronic infection with hepatitis A virus (HAV), hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV), or parvovirus B19 (B19V). Note: If the virus safety test results are indicative of acute or chronic infection with HAV, HBV, HCV, HIV, or B19V, the subject will be considered a screen failure and must be withdrawn from the study.
• Has current evidence of smoking, which includes electronic/vapor cigarettes, or has a positive urine cotinine test at the Week 160/End-of- Study Visit in Study GTi1201 that is due to smoking.
• Has current evidence of chronic alcoholism or illicit drug abuse (addiction).
• Is currently participating in another investigational product (IP) study.
• Has a history of anaphylaxis or severe systemic response to any plasma- derived alpha1-PI preparation or other blood product(s).
• In the opinion of the investigator, is likely to have compliance problems with the protocol and the procedures of the protocol.
• Has any medical condition that the investigator feels might confound the results of the study or pose an additional risk to the subject during study participation.

Where it is running

• Grifols Investigative Site — Phoenix, Arizona, United States
• Grifols Investigative Site — Miami, Florida, United States
• Grifols Investigative Site — Wilmington, North Carolina, United States
• Grifols Investigative Site — Portland, Oregon, United States
• Grifols Investigative Site — Charleston, South Carolina, United States
• Grifols Investigative Site — Tyler, Texas, United States
• Grifols Investigative Site — Darlinghurst, New South Wales, Australia
• Grifols Investigative Site — Adelaide, Australia
• Grifols Investigative Site — Chermside, Australia
• Grifols Investigative Site — Fitzroy, Australia
• Grifols Investigative Site — Nedlands, Australia
• Grifols Investigative Site — Halifax, Canada
• Grifols Investigative Site — Toronto, Canada
• Grifols Investigative Site — Arhus C, Denmark
• Grifols Investigative Site — Hellerup, Denmark
• Grifols Investigative Site — Tallinn, Estonia
• Grifols Investigative Site — Turku, Finland
• Grifols Investigative Site — Bron, Rhone, France
• Grifols Investigative Site — Chisinau, Moldova
• Grifols Investigative Site — Auckland, New Zealand
• Grifols Investigative Site — Christchurch, New Zealand
• Grifols Investigative Site — Hamilton, New Zealand
• Grifols Investigative Site — Krakow, Poland
• Grifols Investigative Site — Warsaw, Poland
• Grifols Investigative Site — Barnaul, Russia

Full record on ClinicalTrials.gov

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