Alvelestat (MPH966) for the Treatment of ALpha-1 ANTitrypsin Deficiency (ATALANTa)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT03679598|
Recruitment Status : Active, not recruiting
First Posted : September 20, 2018
Last Update Posted : April 26, 2023
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|Condition or disease||Intervention/treatment||Phase|
|Alpha-1 Antitrypsin Deficiency (AATD) Pi*ZZ, Pi*SZ, Pi*Null, Another Rare Phenotype/Genotype Known to be Associated With Either Low or Functionally Impaired AAT Including F or I Mutations Emphysema or COPD||Drug: Alvelestat (MPH966) Other: Placebo||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||63 participants|
|Intervention Model:||Parallel Assignment|
|Intervention Model Description:||randomized (1:1), placebo-controlled|
|Masking:||Triple (Participant, Investigator, Outcomes Assessor)|
|Masking Description:||double blind|
|Official Title:||A First in Class Disease Modifying Therapy to Treat Alpha-1 Antitrypsin Deficiency a Genetically Linked Orphan Disease|
|Actual Study Start Date :||April 8, 2019|
|Estimated Primary Completion Date :||June 2023|
|Estimated Study Completion Date :||August 2023|
Active Comparator: Alvelestat (MPH966)
Alvelestat (MPH966) 120mg (4 30mg tablets) twice daily by mouth for 12 weeks
Drug: Alvelestat (MPH966)
Alvelestat was developed as treatment for lung diseases like Chronic Obstructive Pulmonary Disease. Alevelestat works by blocking certain proteins in the body that are responsible for inflammation and damage to the lungs that can lead to COPD symptoms.
Placebo Comparator: Placebo
4 Placebo tablets twice daily by mouth for 12 weeks
Placebo is a pill or tablet that does not contain any study drug.
- Within-individual % change in plasma desmosine/isodesmosine [ Time Frame: baseline, week 12 ]To evaluate the effect of alvelestat (MPH966) administered twice daily (bid) for 12 weeks on blood markers of neutrophil elastase activity, within-individual % change in plasma desmosine/isodesmosine will be measured.
- Numbers and % of subjects who experience at least 1 treatment-emergent adverse event [ Time Frame: baseline, week 16 ]To evaluate the safety and tolerability of alvelestat (MPH966) administered twice daily (bid) for 12 weeks treatment numbers and % of subjects who experience at least 1 treatment-emergent adverse event will be measured.
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|Ages Eligible for Study:||18 Years to 80 Years (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
Participants are eligible to be included in the study only if ALL of the following criteria apply:
- Capable of giving signed informed consent as described in Appendix 3, which includes compliance with the requirements and restrictions listed in the informed consent form and in this protocol
- Age ≥18 and ≤80 years
- Patients with a confirmed diagnosis of AATD: Pi*ZZ, Pi*SZ, Pi*null, or another rare phenotype/genotype known to be associated with either low (serum AAT level <11 μM or <57.2 mg/dL) or functionally impaired AAT including "F" or "I" mutations.
- FEV1 ≥25% predicted
- Patients will be eligible if they are either a) are not currently receiving augmentation treatment and have not received augmentation in the 12 weeks prior to screening or b) have received weekly infusions of augmentation at 60 mg/kg for at least 12 weeks prior to screening and intend to continue augmentation through the study period.
- Male or female sex a. Male participants must agree to use a highly effective contraception as detailed in Appendix 5 during the treatment period and for at least 4 days after the last dose of study treatment and refrain from donating sperm during this period b. Female participants are eligible to participate if not pregnant; not breastfeeding; and at least one of the following conditions is met: i. Not a woman of childbearing potential as defined in Appendix 5 OR ii. A woman of childbearing potential who agrees to follow the contraceptive guidance in Appendix 5. During the treatment phase and for at least 4 days after the last dose of study medication.
Participants are excluded from the study if ANY of the following criteria apply:
Excluded Medical Conditions
- Subjects with Pi*MZ, Pi*FM, Pi*MS, Pi*SS, or other AATD phenotypes/genotypes not known to be independently associated with emphysema.
- Any clinically diagnosed lung disease other than COPD such as diffuse interstitial lung diseases, cystic fibrosis, or clinically significant bronchiectasis as determined by the Investigator
- Acute exacerbation of underlying lung disease requiring oral steroids and/or antibiotics within 4 weeks of baseline
- Acute or chronic hepatitis, including hepatitis B, hepatitis C (positive serologies, including hepatitis B and C antibody)
- HIV infection or other immunodeficiency or with an absolute neutrophil count ≤1.0 × 109/L
- Abnormal liver biochemistry (alanine aminotransferase, aspartate aminotransferase, gamma-glutamyl transferase) >1.5 × upper limit of normal or total bilirubin > upper limit of normal (unless Gilbert's disease with normal conjugated bilirubin)
Any of the following laboratory abnormalities are present at baseline:
- Platelet count <150×109/L
- Serum albumin ≤ 3.5 g/dL
- INR ≥1.2
- CPK ≥ ULN.
- History or current evidence of cirrhosis (on biopsy or imaging), esophageal varices, ascites or hepatic encephalopathy.
- Evidence of other forms of chronic liver disease based on diagnostic testing as per the guidelines (i.e. autoimmune liver disease, primary biliary cirrhosis, primary sclerosing cholangitis, Wilson's disease, Hemochromatosis or iron overload).
- Patients with nonalcoholic fatty liver disease (NAFLD) as diagnosed by any imaging modality (or use of drugs associated with NAFLD for more than 2 weeks in the year prior to screening).
- Subjects with a history of significant alcohol consumption for a period of more than 3 consecutive months within 1 year prior to screening, defined as average of >20g/ day in female subjects and >30g/ day in male subjects.
- Fibrosis-4 (FIB-4) score >3.25
Any of the following cardiovascular conditions within 6 months prior to the screening visit:
- Myocardial infarction or unstable angina
- Coronary artery bypass surgery, balloon angioplasty, percutaneous coronary intervention, or carotid revascularization procedure
- Uncontrolled hypertension
- Stroke or transient ischemic attack
- Congestive heart failure (New York Heart Association III/IV) with left ventricular ejection fraction < 40%
- Any clinically significant 12-lead electrocardiogram abnormalities at screening or baseline, including corrected QT interval by Fridericia's correction method >450 ms or history of significant cardiac dysrhythmia, including long QT syndrome
- History of cancer within the last 5 years, except for well-treated basal cell carcinoma and squamous cell carcinoma of the skin
Other documented comorbidities or laboratory abnormalities that in the opinion of the Investigator could affect the outcome of the study assessments, participant safety, or ability of the participant to comply with the requirements of the protocol
Excluded Prior/Concomitant Therapy
- Daily use of prednisone (>10mg daily), or other systemic glucocorticoids at comparable or higher equivalent dose, or use of other immunosuppressant therapies are prohibited
- Immunomodulating monoclonal antibodies within 6 months prior to screening are prohibited
- Daily use of non-steroidal anti-inflammatory drugs (NSAIDs) is prohibited. Daily use of acetaminophen up to 2 g per day and aspirin up to 325 mg per day is permitted.
Initiation of drugs known for hepatotoxic potential within the 28 days prior to screening including but not limited to: statins, NSAIDS, amoxicillin/clavulanate, PDE inhibitors (theophylline, roflumilast), and anti-epileptics. Subjects on established treatment for more than 28 days prior to screening will not be excluded. Requirement for medications mainly metabolized by CYP2C9 and with narrow therapeutic index (eg, warfarin, phenytoin) is prohibited
Excluded Prior/Concurrent Clinical Study Experience
- Participation in any clinical investigation using medical devices or non-biologic treatments within 4 weeks or 5 half-lives of the drug (whichever is longer) prior to the initial dosing (or longer if required by local regulations) is prohibited
- Participation in any clinical investigation using biologic treatment within 6 months of screening is prohibited
Previous participation in a gene therapy study for AATD at any time is prohibited
- History of hypersensitivity to alvelestat (MPH966) or any of its excipients or the class of neutrophil elastase inhibitors
- Known hypersensitivity to medications used in the study procedures (e.g. midazolam, fentanyl, and lidocaine for bronchoscopy)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03679598
|United States, Alabama|
|The University of Alabama at Birmingham Lung Health Center|
|Birmingham, Alabama, United States, 35294|
|United States, California|
|Los Angeles, California, United States, 90095|
|United States, Colorado|
|National Jewish Health|
|Denver, Colorado, United States, 80206|
|United States, New York|
|New York, New York, United States, 10032|
|United States, North Carolina|
|University of North Carolina at Chapel Hill|
|Chapel Hill, North Carolina, United States, 27517|
|United States, Ohio|
|Cleveland, Ohio, United States, 44195|
|United States, Pennsylvania|
|Philadelphia, Pennsylvania, United States, 19140|
|United States, South Carolina|
|Medical University of South Carolina|
|Charleston, South Carolina, United States, 29425-6300|
|United States, Texas|
|The University of Texas Health Science Center at Tyler|
|Tyler, Texas, United States, 75708|
|United States, Utah|
|University of Utah|
|Salt Lake City, Utah, United States, 84108|
|Principal Investigator:||Mark T Dransfield, MD||University of Alabama at Birmingham|
|Responsible Party:||Mark Dransfield, MD, Professor, University of Alabama at Birmingham|
|Other Study ID Numbers:||
4UH3TR002450-02 ( U.S. NIH Grant/Contract )
|First Posted:||September 20, 2018 Key Record Dates|
|Last Update Posted:||April 26, 2023|
|Last Verified:||April 2023|
|Studies a U.S. FDA-regulated Drug Product:||Yes|
|Studies a U.S. FDA-regulated Device Product:||No|
Alpha 1-Antitrypsin Deficiency
Respiratory Tract Diseases
Digestive System Diseases
Genetic Diseases, Inborn