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

Phase 2

Completed

Conditions: Alpha-1 Antitrypsin Deficiency

Interventions: Drug: Kamada-AAT for Inhalation, 80mg
Drug: Placebo
Drug: Kamada-AAT for Inhalation, 160mg

Registration Number: NCT02001688

Lead Sponsor: Kamada, Ltd.

Brief Summary: 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.

Detailed Description: Not available

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 36

Inclusion Criteria

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.

Exclusion Criteria

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.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Kamada-AAT for Inhalation, 80mg	Kamada-AAT for Inhalation, 80mg	Daily inhalation of Kamada-AAT for Inhalation, 80mg
Placebo	Placebo	Placebo administered by inhalation daily
Kamada-AAT for Inhalation, 160mg	Kamada-AAT for Inhalation, 160mg	Daily inhalation of Kamada-AAT for Inhalation, 160mg

Primary Outcome Measures

Name	Time	Method
Change From Baseline in the Concentration of Antigenic Alpha-1 Antitrypsin (AAT) in the Lung Epithelial Lining Fluid (ELF)	12 weeks from initiation of study drug	Patients underwent bronchoalveolar lavage (BAL) prior to initiation of drug and then again after 3 months. Concentration of AAT in the BAL was measured by an enzyme linked immunosorbent assay (ELISA) specific for the normal form of AAT (piM). Urea was also measured in order to determine the dilution factor of the BAL fluid and calculate the concentration of AAT in the ELF.
Change From Baseline to 12 Weeks in the Concentration of Functional AAT (Alpha-1 Antitrypsin) in ELF	12 weeks from initiation of study drug	ITT population with baseline and 12 week values. Patients underwent bronchoalveolar lavage (BAL) prior to initiation of drug and then again after 3 months. Concentration of AAT in the BAL was measured by an antineutrophil elastase capacity (ANEC) assay. Urea was also measured in order to determine the dilution factor of the BAL fluid and calculate the concentration of AAT in the ELF.

Secondary Outcome Measures

Name	Time	Method
Change From Baseline in Levels of M Specific AAT in Plasma (PiM)	12 weeks from initiation of study drug	Intention to treat (ITT) population with baseline and 12 week values.The median change from baseline to Week 12 in the levels of M-specific AAT (piM) in plasma was measured using a specific ELISA assay for M-specific AAT (piM)
Change From Baseline in AAT-neutrophil Elastase (NE) Complexes in ELF	12 weeks from initiation of study drug	Patients underwent a BAL procedure at baseline and 12 weeks and the fluid was analyzed to calculate the change from baseline in the concentration of complexes between AAT and neutrophil elastase in the ELF

Trial Locations

Locations (2): The University of Texas Health Science Center at Tyler Center for Clinical Research
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Tyler, Texas, United States
University of Florida, Pulmonary, Critical Care & Sleep Medicine
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Gainesville, Florida, United States