Phase II, Safety and Efficacy Study of Kamada-alpha-1-antitrypsin (AAT) for Inhalation"

Completed · Phase 2 · Has a placebo group

Conditions studied: Alpha-1 Antitrypsin Deficiency

In brief

To evaluate different doses of "Kamada-AAT for Inhalation" on the levels of alpha 1-proteinase inhibitor and other analytes in epithelial lining fluid (ELF) and serum and to assess the safety of the treatment in subjects with AAT Deficiency.

Key facts

Study ID

NCT02001688

Run by

Kamada, Ltd.

People needed

36

Starts

2014-04-01

Expected to finish

2016-05-01

Last updated by the study team

2020-01-18

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female patients between 18 and 65 years of age (inclusive).
• Able and willing to sign informed consent.
• Males, and non-pregnant, non-lactating females whose screening pregnancy test is negative and who are using contraceptive methods deemed reliable by the investigator or who are post-menopausal or surgically sterilized.
• Diagnosis of alpha1-antitrypsin deficiency [only individuals with a ZZ or Z null classification].
• Forced expiratory volume in one second (FEV1) ≥ 50% of predicted post bronchodilator
• No respiratory exacerbations within 6 weeks of baseline. Subjects can be re-screened if exacerbations exist at the time of enrollment.
• No signs of chronic and/or acute Hepatitis A, Hepatitis B, Hepatitis C, HIV infection and Parvovirus B19, by NAT (for Parvovirus B19, nucleic acid testing (NAT) result must be < 10\^4 IU/mL).
• No significant abnormalities in serum hematology, serum chemistry, serum inflammatory / immunogenic markers and urinalysis.
• No significant abnormalities in ECG.
• Not on intravenous augmentation therapy for at least 8 weeks prior to initial dosing with study drug/placebo and willing to forego intravenous augmentation therapy for the duration of the study.

You may not qualify if…

• Clinically significant intercurrent illnesses (except for respiratory or liver disease secondary to AAT deficiency), including: cardiac, hepatic, renal, endocrine, neurological, hematological, neoplastic, immunological, skeletal or other) that in the opinion of the investigator, could interfere with the safety, compliance or other aspects of this study. Patients with well-controlled, chronic diseases could possibly be included after consultation with the treating physician and the sponsor.
• History of life threatening allergy, anaphylactic reaction, or systemic response to human plasma derived products.
• History of life threatening transfusion reactions.
• History of lung transplant.
• Current or previous (up to 8 weeks from baseline) use of AAT augmentation therapy or by any other route
• Current use of oral or parenteral glucocorticoids in doses exceeding 10mg of prednisone daily or equivalent generics (substance and dose).
• Any lung surgery within the past two years.
• On any thoracic surgery waiting list.
• Active smoking during the last 12 months from screening date.
• Pregnancy or lactation.
• Woman of child-bearing potential not taking adequate contraception deemed reliable by the investigator.
• Presence of psychiatric/ mental disorder or any other medical disorder which might impair the patient's ability to give informed consent or to comply with the requirements of the study protocol.
• Evidence of alcohol abuse or history of alcohol abuse or illegal and/or legally prescribed drugs.
• Immunoglobulin A (IgA) Deficiency.
• Inability to undergo bronchoscopy.
• Allergy to lidocaine or any other medicines used in the bronchoscopy process
• Exacerbation of chronic obstructive pulmonary disease (COPD) in the previous 6 weeks.
• Participation in another clinical trial involving investigational medication or interventional treatment within 30 days prior to baseline visit.
• Participation in observational clinical trial which involves any invasive procedure scheduled to occur during the AAT inhaled study period. If participating in an observational clinical trial that already completed all diagnostic procedures (e.g. liver biopsy), any adverse events (AEs) experienced must have returned to baseline within 30 days prior to baseline visit.
• Inability to attend scheduled clinic visits and/or comply with the study protocol.
• Any other factor that, in the opinion of the investigator, would prevent the patient form complying with the requirements of the protocol.

Where it is running

• University of Florida, Pulmonary, Critical Care & Sleep Medicine — Gainesville, Florida, United States
• The University of Texas Health Science Center at Tyler Center for Clinical Research — Tyler, Texas, United States

Full record on ClinicalTrials.gov

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