A Safety and Biomarker Study of ALZT-OP1a in Subjects With Mild-Moderate ALS Disease

Amyotrophic Lateral Sclerosis Clinical Trial

Official title:

A Phase IIa, Randomized, Open-label, Multi-Center, Multi-Dose Study to Evaluate the Effects of ALZT-OP1a in Subjects With Mild-Moderate Stage Amyotrophic Lateral Sclerosis (ALS)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04428775
• Other study ID #: AZT-006
• Status: Terminated
• Phase: Phase 2
• Start date: September 8, 2020
• Est. completion date: October 1, 2021

Study information

• Verified date: June 2021
• Source: AZTherapies, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase IIa, randomized, open-label, multi-center, multi-dose study for subjects with mild to moderate ALS. The protocol is designed to determine whether ALZT-OP1a treatment will positively impact neuro-inflammatory biomarkers and slow down or arrest functional decline in subjects with mild to moderate ALS.

Description:

This Phase IIa study is designed as a randomized, open-label, multi-center, multi-dose study for subjects with mild to moderate ALS. The study will evaluate 1) safety, 2) tolerability, 3) changes in physical function measured using the ALSFRS-R, 4) two doses of ALZT-OP1a in order to determine an optimal and effective dose that could positively impact neuro-inflammatory biomarkers, and 5) to demonstrate preliminary evidence if this treatment could potentially slow down or arrest functional decline in subjects with mild to moderate ALS. Up to 80 evaluable subjects will be randomly assigned to one of two treatment groups: Group I (n=40) will consist of low dose ALZT-OP1a, administered via dry powder inhalation; OR Group II (n=40), which will consist of high dose ALZT-OP1a, administered via dry powder inhaler. Subjects will dose for 12 weeks and will be asked to return to the site for scheduled visits and biomarker collection at Week 4, Week 8, and Week 12.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 12
• Est. completion date: October 1, 2021
• Est. primary completion date: October 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Male or female subjects aged 18-75 years, both inclusive;
• Must provide written informed consent before any study related procedures;
• Should be capable to complete all trial related procedures, assessments and visits in the judgement of Investigator;
• Familial or sporadic ALS diagnosed as possible, laboratory-supported probable, probable, or definite as defined by revised El Escorial criteria;
• Disease duration from ALS diagnosis =24 months;
• ALSFRS-R total score = 36 at screening visit;
• ALSFRS-R Breathing sub-score should be =9 at the time of screening;
• ALSFRS-R Bulbar sub-score should be =9 at the time of screening;
• Peak inspiratory flow rate (PIFR) = 100 L/minute;
• Forced vital capacity (FVC) >70% of predicted value;
• Participant must be receiving treatment with stable dose of standard of care treatment for =30 days prior to signing informed consent.

Exclusion Criteria:

• Subjects with bulbar-onset ALS;
• Any use of non-invasive ventilation (e.g., continuous positive airway pressure, non-invasive bi-level positive airway pressure or non-invasive volume ventilation) for any portion of the day, or mechanical ventilation via tracheostomy, or on any form of oxygen supplementation;
• Any other significant neurological disorder which can interfere with study assessments, e.g., significant cognitive impairment and/or clinical dementia;
• Significant psychiatric illness like schizophrenia, bipolar disorder etc. Subjects with depression can be included, only if the depression has been stable and no episode of major depression has occurred in past one year;
• Severe cardiac disease (e.g.,corrected QT interval > 500ms), Torsade de Pointes, evidence of significant heart failure (New York Heart Association [NYHA] Class 3 or greater, myocardial infarction or unstable angina in the 6 months prior to screening);
• Any moderate-to-severe pulmonary disease or difficulty taking inhaled drugs;
• Inability to tolerate the administration of an oral inhaled powder via dry powder inhaler (DPI);
• Has taken any investigational study drug within 30 days or five half-lives of the drug, whichever is longer, prior to dosing;
• Currently taking cromolyn, or has taken cromolyn, within the past 12 months;
• Allergy to cromolyn or cromolyn products, such as Intal®, Nasalcrom®, Opticrom®, Gastrocrom®, etc.;
• Taking inhaled protein products on a chronic basis (such as insulin, parathyroid hormone [PTH], etc.);
• Subjects who weigh 88 lb (40 kg) or less, or, body mass index (BMI) of <17.5 or >35.0 at screening;
• Moderate-to-severe liver disease: aspartate aminotransferase (AST), alanine aminotransferase (ALT), or bilirubin concentrations >3 times the upper limit of normal; patients with hepatic diseases such as hepatic cirrhosis, hepatic cancer and active hepatitis
• Moderate-to-severe renal disease: creatinine clearance <45 mL/min/1.73 m2 (by Cockcroft-Gault calculation);
• Any clinically significant disorder or laboratory abnormality that, in the investigator's opinion, could interfere with the subject's participation in the study, place the subject at increased risk, or confound interpretation of the study results;
• Pregnant or breast-feeding females or sexually active females with childbearing potential, if no adequate contraceptive measures are used.

Related Conditions & MeSH terms

• Amyotrophic Lateral Sclerosis
• Motor Neuron Disease
• Sclerosis

Intervention

Drug:
• ALZT-OP1a (cromolyn)
Mast cell stabilizer Neuroinflammatory microglial modulator anti-inflammatory

Locations

Country	Name	City	State
United States	Mayo Clinic	Jacksonville	Florida
United States	UCSD Altman Clinical and Translational Research Institute	La Jolla	California
United States	Columbia University Medical Center	New York	New York
United States	Hospital for Special Surgery	New York	New York
United States	Oregon Health & Science University	Portland	Oregon
United States	Wake Forest School of Medicine	Winston-Salem	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
AZTherapies, Inc.

Country where clinical trial is conducted

United States, 

References & Publications (1)

Granucci EJ, Griciuc A, Mueller KA, Mills AN, Le H, Dios AM, McGinty D, Pereira J, Elmaleh D, Berry JD, Paganoni S, Cudkowicz ME, Tanzi RE, Sadri-Vakili G. Cromolyn sodium delays disease onset and is neuroprotective in the SOD1(G93A) Mouse Model of amyotrophic lateral sclerosis. Sci Rep. 2019 Nov 27;9(1):17728. doi: 10.1038/s41598-019-53982-w. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Plasma Biomarkers	To measure the effect of ALZT-OP1a treatment on selected plasma biomarkers in ALS patients.; Candidate biomarkers in ng/mL include: Beta-tryptase, Beta-Hexosaminidase; Candidate biomarkers in pg/mL include: CXCL1, interferon-y, interleukin (IL)-1a, IL-1b, IL-2, IL-5, IL-6, IL-8, IL-10, IL-15, IL-17, macrophage inflammatory protein (MIP)-1a, MIP-1b, monocyte chemoattractant protein (MCP)-1, neurofilament light protein (NfL), tumor necrosis factor (TNF)-a, and vascular endothelial growth factor (VEGF)	up to 12 weeks
Secondary	Changes from baseline in ALS disease progression	Measured by ALS Functional Rating Scale-Revised (ALSFRS-R) - Questionnaire	up to 12 weeks
Secondary	Time to Event Requiring Respiratory Support	Measured by the time to event requiring full-time or nearly full-time respiratory support from baseline by treatment arm.	up to 12 weeks
Secondary	Changes from baseline in pulmonary function (forced vital capacity)	Measured by changes in forced vital capacity (FVC) in percent predicted value from baseline by treatment arm.	up to 12 weeks
Secondary	Changes from baseline in pulmonary function (peak inspiratory flow rate)	Measured by changes in peak inspiratory flow rate (PIFR) in liters per minute from baseline by treatment arm.	up to 12 weeks
Secondary	Incidence of adverse event (tolerability) related to ALZT-OP1a	Evaluated by number and percentage of unexpected adverse events by treatment arm.	up to 12 weeks
Secondary	Number of participants with abnormal vital signs	Measured by changes in systolic / diastolic blood pressure, pulse rate, respiratory rate, and body temperature from baseline by treatment arm.; The data will also be presented in shift tables as within normal limits, clinically significant, not clinically significant.	up to 12 weeks
Secondary	Number of participants with abnormal physical or neurological examinations	Review of all body systems and changes evaluated for clinical significance from baseline by treatment arm.; The data will also be presented in shift tables as within normal limits, clinically significant, not clinically significant.	up to 12 weeks
Secondary	Number of participants with abnormal electrocardiograms (ECGs)	Measured by changes in heart rate, PR interval, QRS complex, and QT interval from baseline by treatment arm.; The data will also be presented in shift tables as within normal limits, clinically significant, not clinically significant.	up to 12 weeks
Secondary	Number of participants with treatment emergent clinically significant laboratory assessments	The abnormal values will be presented by treatment arm from baseline.; The data will also be presented in shift tables as within normal limits, clinically significant, not clinically significant.	up to 12 weeks
Secondary	Changes from baseline in suicidal ideation and behavior	Measured by changes in Columbia Suicide Severity Rating Scale (C-SSRS) from baseline; minimum score: 0 maximum score: 10; lower values represent a better outcome.	up to 12 weeks
Secondary	The number of study dropouts due to serious, unanticipated treatment emergent adverse events	The dropouts will be presented by treatment arm from baseline.	up to 12 weeks