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Safety and Efficacy of P-188 NF in DMD Patients

key information

study id #: NCT03558958

condition: Duchenne Muscular Dystrophy

status: recruiting

purpose:

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.

intervention: P-188 NF

mechanism of action: Membrane-sealing poloxamer to repair membrane instabilities

results: https://clinicaltrials.gov/ct2/show/results/NCT03558958

last updated: September 09, 2019

study details

start date: August 8, 2018

estimated completion: September 2020

phase of development: Phase 2

size / enrollment: 10

study 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.

primary outcomes:

  • Forced vital capacity (FVC) [ Time Frame: Baseline, Days 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)

secondary outcomes:

  • Maximal inspiratory pressure (MIP) [ Time Frame: Baseline, Days 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Maximal expiratory pressure (MEP) [ Time Frame: Baseline, Days 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Peak cough flow (PCF) [ Time Frame: Baseline, Days 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Left ventricular end-diastolic volume (LVEDV) [ Time Frame: Baseline, Days 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Ejection Fraction (EF) [ Time Frame: Baseline, Days 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Degree of fibrosis as assessed by cardiac MRI [ Time Frame: Baseline, Days 182, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Performance of upper limb (PUL) test [ Time Frame: Baseline, Days 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Cardiac troponin I [ Time Frame: Baseline, Days 28, 56, 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)
  • Muscle creatine kinase [ Time Frame: Baseline, Days 28, 56, 91, 182, 273, 364 ]
    Change from baseline (pre-treatment) to end of treatment (52 weeks)

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

study contacts

sponsor: Phrixus Pharmaceuticals, Inc.

investigators: Thomas Ryan (MD); Children's Hospital Medical Center, Cincinnati

locations: United States