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S 48168 (ARM 210) for the Treatment of RYR1-related Myopathies (RYR1-RM)

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: NCT04141670
Recruitment Status : Active, not recruiting
First Posted : October 28, 2019
Last Update Posted : July 19, 2022
Sponsor:
Collaborators:
National Institute of Neurological Disorders and Stroke (NINDS)
National Institute of Nursing Research (NINR)
Celerion
Information provided by (Responsible Party):
Armgo Pharma, Inc.

Brief Summary:
This study proposes to test S 48168 (ARM210) in a Phase 1 trial in RYR1-RM patients, specifically. The objectives of this study are to explore the safety and tolerability, pharmacokinetics (PK), pharmacodynamics (PD)/target engagement (TE) of S 48168 (ARM210), as well as effects on muscle/motor function, and fatigue in RYR1-RM patients. The study population will include adult patients (≥18 years of age) who have demonstrated leaky RyR1 channels that are responsive to S48168 (ARM210) ex vivo.

Condition or disease Intervention/treatment Phase
RYR-1 Myopathy Drug: S48168 Phase 1

Detailed Description:

RYR1- related myopathy comprises a group of rare neuromuscular diseases. Affected individuals generally present with delayed motor milestones, muscle weakness, impaired ambulation, and, in severe cases, scoliosis, ophthalmoplegia, and respiratory distress all due to skeletal muscle weakness.

Causative variants in RYR1, which encodes the major calcium (Ca2+) release channel in skeletal muscle, RyR1, exert different effects on the RyR1 channel. They generally disrupt the normal Ca2+ flow between the sarcoplasmic reticulum (SR) and muscle cell cytosol and commonly result in excessive Ca2+ leak into the cytosol. Persistent Ca2+ leaks reduce its availability in the SR that is necessary for excitation-contraction coupling leading to the muscle weakness characteristic of this disease.

This open-label study consists of ten participants, randomized to two dose groups. All participants will have a diagnosis of RYR1-RM. In addition they have a prior muscle biopsy demonstrating a leaky RYR1 channel which responds to S48168 (ARM210) ex vivo. The first group of three participants will receive a low dose of S 48168 (ARM210) daily for 28 days. The second group of seven participants will receive a higher dose for 28 days. The decision to escalate to the higher dose will be made by an independent Data and Safety Monitoring Board (DSMB) after review of safety, tolerability and PK of the low daily dose. Safety and tolerability will be the primary objective in this study. In addition, exploratory objectives will include PK, PD/TE as well as measures of muscle/motor function and fatigue.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 10 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Safety and Tolerability of S 48168 (ARM 210) for the Treatment of RYR1-related Myopathies (RYR1-RM)
Actual Study Start Date : August 25, 2020
Actual Primary Completion Date : June 30, 2022
Estimated Study Completion Date : September 30, 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Muscle Disorders

Arm Intervention/treatment
Experimental: Low dose group
Experimental: Low dose group Group of three participants who are treated with a low dose of S48168 (ARM210) for 28 days.
Drug: S48168
A novel oral small molecule which is designed to repair leaky RYR1 channels
Other Name: ARM 210

Experimental: High dose group
Experimental: High dose group Group of seven participants who are treated with a high dose of S48168 (ARM210) for 28 days.
Drug: S48168
A novel oral small molecule which is designed to repair leaky RYR1 channels
Other Name: ARM 210




Primary Outcome Measures :
  1. Safety and tolerability of S48168 (ARM210) treatment in RYR1-RM affected individuals [ Time Frame: 42 days ]
    Composite safety and tolerability profile of S48168 (ARM210)



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

INCLUSION CRITERIA:

Patients must meet all the following conditions to be eligible for enrollment into the study:

  1. Body mass index (BMI) ≥ 18.0 and ≤ 36.0 kg/m2 at screening.
  2. Confirmed genetic diagnosis of RYR1-RM and supporting clinical phenotype.
  3. Ambulatory. Able to walk ten meters (with or without assistance e.g. with a cane).
  4. Prior muscle biopsy with demonstrated leaky RyR1 channel.
  5. Must have a CYP2C8 extensive or intermediate metabolizer genotype.
  6. Daily use of medicines and dietary supplements need to be approved by the PI and Sponsor, or a drug/supplement-dependent wash-out prior to inclusion.
  7. For male subjects: is sterile or agrees to use an appropriate method of contraception, including a condom with spermicide, from study drug administration on the first day of dosing until 5 half-lives plus 90 days (approximately 94 days) after the last dose of study drug administration. No restrictions are required for a vasectomized male subject provided the subject is at least 1-year post-bilateral vasectomy procedure prior to study drug administration on first day of the first dose. A male subject whose vasectomy procedure was performed less than 1 year prior to study drug administration on the first day of dosing must follow the same restrictions as a non-vasectomized male. Appropriate documentation of surgical procedure should be provided.
  8. For male subjects: agrees to not donate sperm from study drug administration on the first day of dosing until 5 half-lives plus 90 days (approximately 94 days) after the last dose of study drug.
  9. For female subjects of childbearing potential: uses one of the following highly effective birth control methods:

    • Prescribed hormonal oral contraceptives, vaginal ring, or transdermal patch.
    • Intrauterine device (IUD).
    • Intrauterine hormone-releasing system (IUS).
    • Depot/implantable hormone (e.g., Depo-provera®, Implanon).
    • Bilateral tubal occlusion/ligation.
    • Sexual abstinence:
    • Refraining from heterosexual intercourse during the entire period of risk associated with the study requirements.
    • If the participant decides to become sexually active during the study, then one of the highly effective birth control methods must be used.
  10. For female subjects of non childbearing potential; defined by at least 1 of the following criteria:

    • Postmenopausal defined as 12 months of spontaneous amenorrhea and follicle stimulating hormone (FSH) serum level > 40mIU/mL. Appropriated documentation of FSH levels is required.
    • Surgically sterile by hysterectomy and/or bilateral oophorectomy with appropriate documentation of surgical procedure.
    • Has a congenital condition resulting in no uterus.
  11. Willingness and ability to comply with scheduled visits, drug administration plan, laboratory tests, study restrictions, and study procedures (muscle biopsies and PK sampling).
  12. Able to provide written informed consent and understands the study procedures in the informed consent form (ICF).

EXCLUSION CRITERIA:

The presence of any of the following conditions will exclude a patient from study enrollment:

  1. Patient is mentally or legally incapacitated at the time of the screening visit or during the conduct of the study.
  2. History or presence of alcoholism or drug abuse within the past 2 years prior to the first dose of study drug.
  3. History or presence of hypersensitivity or idiosyncratic reaction to the study drug, related compounds, or inactive ingredients.
  4. Positive urine drug or alcohol results at screening.
  5. Positive results at screening for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV).
  6. Patients with baseline ALT levels three times above the upper limits of normal (ULN) or baseline AST levels five times the ULN (isolated elevations of total bilirubin <2 X ULN with direct bilirubin below the ULN will be included).
  7. Patients with severe pulmonary dysfunction at screening (Forced Vital Capacity (FVC) < 50% predicted) or evidence of pulmonary exacerbation. Pulmonary exacerbations refer to an acute worsening of respiratory symptoms that result from a decline in lung function.
  8. Patients with a history of a seizure.
  9. Subject has a history of cancer (malignancy) Exceptions: (1) Subjects with adequately treated non-melanomatous carcinoma or carcinoma in situ of the cervix may participate in the trial (2) Subjects with other malignancies who have been successfully treated > 10 years prior to the screening where in the judgment of the investigator has revealed no evidence of recurrence from the time of treatment through the time of the screening except those identified at the beginning of the exclusion criterion or (3) Subjects who in the opinion of the investigator are highly unlikely to sustain a recurrence for the duration of the trial.
  10. Patients with uncontrolled diabetes defined as HbA1c > 7% or diabetic neuropathy.
  11. Estimated creatinine clearance <40 mL/minute at screening, which may be calculated using the Chronic Kidney Disease Epidemiology Collaborative method (CKD-EPI), due to reduced muscle mass often seen in RYR1-RM patients.
  12. Patients with a clinically significant abnormality on their ECG other than hypertensive related, or heart failure (ejection fraction <30%) or other clinically significant structural heart disease on echocardiogram.
  13. Patients with a history of myocardial infarction in the last five years, or evidence of congestive heart failure.
  14. Pregnant and breastfeeding women.
  15. Patients who have taken Aspirin, Ibuprofen, or Naproxen within the 3 days prior to the muscle biopsy procedure, and/or patients who have taken Plavix (clopidogrel) or Brilinta (ticagrelor) 5 days prior to the muscle biopsy.
  16. Unable to refrain from or anticipates the use of:

    • Any non-approved medicines and/or dietary supplements beginning 14 days prior to the first dose of study drug and throughout the study. Thyroid hormone replacement medication may be permitted if subject has been on same stable dose for the last 3 months prior to the first dose of study drug. Medicines that would contraindicate the skeletal muscle needle biopsy procedure, and therefore would be considered non- approved, include but are not limited systemic anticoagulants or oral direct thrombin inhibitors.
    • Any drugs known to be significant inducers or inhibitors of CYP2C8 enzymes for 28 days prior to the first dose of study drug and throughout the study. Any substrates of breast cancer resistance protein (BCRP).
  17. Is currently taking any drug which raises gastric pH, including proton pump inhibitors or H2 antagonists. Antacids may be used if taken at night.
  18. Donation of blood or significant blood loss within 56 days prior to the first dose of study drug.
  19. Plasma donation within 7 days prior to the first dose of study drug.
  20. Participation in clinical trials for other therapeutic investigational drugs simultaneously or within the 4 weeks prior to the first dose of study drug.
  21. Ongoing medical condition that is deemed by the Principal Investigator to interfere with the conduct or assessments of the study or safety of the subject.
  22. Is an NIH employee who is a subordinate/relative/coworker of a study investigator.

Information from the National Library of Medicine

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): NCT04141670


Locations
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United States, Maryland
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Sponsors and Collaborators
Armgo Pharma, Inc.
National Institute of Neurological Disorders and Stroke (NINDS)
National Institute of Nursing Research (NINR)
Celerion
Investigators
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Principal Investigator: Payam Mohassel, M.D. National Institute of Neurological Disorders and Stroke (NINDS)
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Responsible Party: Armgo Pharma, Inc.
ClinicalTrials.gov Identifier: NCT04141670    
Other Study ID Numbers: 200005
1ZIANS003129-08 ( U.S. NIH Grant/Contract )
Bench-to-bedside award 551673 ( Other Grant/Funding Number: Intramural NINR )
First Posted: October 28, 2019    Key Record Dates
Last Update Posted: July 19, 2022
Last Verified: July 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: all IPD that underlie results in a publication
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Clinical Study Report (CSR)
Time Frame: six months after publication
Access Criteria: published results and associated data will be available to academic medical researchers and patient advocacy groups upon request from ARMGO Pharma, INC

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Armgo Pharma, Inc.:
RYR1
Myopathy
Additional relevant MeSH terms:
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Muscular Diseases
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases