Safety and Efficacy of P-188 NF in DMD Patients

Phrixus Pharmaceuticals

Status and phase

Terminated

Phase 2

Conditions

Duchenne Muscular Dystrophy

Treatments

Drug: P-188 NF

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT03558958

P-004

Details and patient eligibility

About

This is an open-label study to evaluate the safety, tolerability and efficacy of daily, subcutaneous dosing with P-188 NF (Carmeseal-MD™) in non-ambulatory boys with Duchenne Muscular Dystrophy (DMD). This study will determine if continuous treatment with Carmeseal-MD™ can maintain or improve pulmonary function, and skeletal and cardiac muscle function, compared to baseline, in boys 12-25 years of age.

Full description

Based on a large number of studies conducted in pre-clinical models of muscular dystrophy and heart failure, this study is being undertaken to explore the safety and efficacy of Carmeseal-MD™ (P-188 NF) on endpoints associated with cardiovascular, pulmonary and musculoskeletal function. These preclinical studies indicate that Carmeseal-MD™ acts to stabilize fragile cell membranes thus maintaining cell function and preventing fibrosis, necrosis and apoptosis in animal models of muscular dystrophy.

This is a single arm, open label trial that is designed to provide a first evaluation of Carmeseal-MD™ in non-ambulatory patients with DMD. It assigns up to ten (10) patients to receive a fixed dose of 5 mg of P-188 NF per Kg patient body weight (adjusted individually for each patient at baseline visit) injected subcutaneously once-a-day for 52 weeks. The first 3 enrolled subjects (Group 1) will be at least 18 years of age and up to 25 years of age. Enrollment of Group 2 will begin after a review of Group 1 safety data through 28 days of dosing of Carmeseal-MD™. Group 2 will include subjects that are at least 12 years of age and up to 25 years old. Evaluations will be for Carmeseal-MD™ administered in addition to the current standard of care therapies and interventions such as corticosteroids, ACE inhibitors, ARBs, beta blockers, bronchodilator medications and airway clearance, cough assist and non-invasive ventilation devices.

The major hypothesis for the trial is that measures of function of skeletal and cardiac muscle that decline over the course of the disease will either remain stable or improve with P-188 NF treatment when a decline would be expected. To assess these possible beneficial effects, comparisons are planned between pre- and post-treatment on measures of function for the various body systems affected by DMD.

Enrollment

2 patients

Sex

Male

Ages

12 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male
12 - 25 years of age
Have phenotypic evidence of DMD
Have documentation of the presence of a deletion, duplication or point mutation in the dystrophin gene
Willingness to receive daily subcutaneous (SC) injections of up to 3 mL
Have LVEDV that is ≥100% of normal corrected for body mass when measured by cardiac MRI
Have impaired respiratory function (percent predicted PEF ≤80%)
Have ability to perform PEF within 15% of first assessment
Have mild to moderate fibrosis of the heart as assessed by MRI
Have left ventricular ejection fraction fractions of <50%
Have been non-ambulatory for at least six months
Be on corticosteroids, with a stable treatment regimen for at least six months
Have been on a stable treatment regimen for cardiac dysfunction for at least 3 months prior to baseline (ACE inhibitors, beta blockers and/or ARBs)
Have clinically acceptable screening values, including serum creatinine levels blood urine nitrogen, cystatin C
Have willingness and ability to comply with scheduled visits, drug administration, drug administrative plan, study procedures, laboratory tests, and treatment restrictions
Be likely to survive for the duration of the treatment in the investigator's opinion
Have ability to provide written informed consent (parent/guardian consent if applicable)/assent (if <18 years of age).

Exclusion criteria

Exposure to another investigational drug within 90 days prior to start of study treatment
Have DMD-related hypoventilation for which daytime assisted ventilation is needed
Unable to perform pulmonary function testing
Have respiratory failure
Unable or unwilling to undergo scan with gadolinium as contrast agent
Unable or unwilling to undergo echocardiography
Have severe fibrosis of the heart as assessed by MRI
Used carnitine, creatine, glutamine, oxatomide, coenzyme Q10 or vitamin E or any herbal medicines with 30 days prior to baseline
Have a history of major surgical procedure within 30 days prior to start of study treatment
Have ongoing immunosuppressive therapy (other than corticosteroids)
Are participating in a therapeutic clinical trial
Are on any concomitant medication with a depressive or stimulating effect on respiration or the respiratory tract
Have a diagnosis of chronic lung disease
Chronic use of beta-2 agonists or any other bronchodilating medication (chronic use is daily intake for more than 14 days within the last 6 months)
Have moderate or severe hepatic impairment or moderate to severe renal impairment
Have expectation of major surgical procedure during the conduct of the study
Have prior or ongoing medical conditions that makes it unlikely that the course of treatment or follow-up would be completed, or could impair the assessment of the treatment results
Have ever previously received P-188 NF as a therapeutic agent