NCT02796937
Long Term Safety of Alpha1-Proteinase Inhibitor in Subjects With Alpha1 Antitrypsin Deficiency
Enrolling by Invitation
PHASE3Ages 20–72InterventionalTreatmentGrifols Therapeutics LLC
~290 participants
Updated 2026-06-23 on ClinicalTrials.gov
What's tested:Alpha-1 MP
At a glance
Recruiting sites
0 of 28 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Adverse events (AEs)
Measured over Week 1 through Week 108
+2 more outcomes measured
Conditions
Where it's being run
28 sites across 18 statesAustralia4
New Zealand3
Sweden3
Canada2
Denmark2
Poland2
Arizona1
Florida1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
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
Exclusion
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.
What this trial measures
- Adverse events (AEs)Week 1 through Week 108
Monitoring of AEs
- Serious AEs (SAEs)Week 1 through Week 108
Monitoring of SAEs
- Discontinuations from the study due to AEsWeek 1 through Week 108
Monitoring of discontinuations due to AEs