Exploratory Study of NS-065/NCNP-01 in DMD

Exploratory Study of NS-065/NCNP-01 in Duchenne Muscular Dystrophy

This study is designed to assess the safety, tolerability, efficacy and pharmacokinetics (PK) of NS-065/NCNP-01 in subjects diagnosed with Duchenne muscular dystrophy (DMD).

Study Overview

• Status: Completed
• Conditions: Duchenne Muscular Dystrophy
• Intervention / Treatment: Drug: NS-065/NCNP-01

• Study Type: Interventional
• Enrollment (Actual): 10
• Phase: Phase 1

Contacts and Locations

Study Locations

• Japan
  • Tokyo
    • Kodaira, Tokyo, Japan, 1878551
      • National Center of Neurology and Psychiatry

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 1 year to 14 years (Child, Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Male

Description

Inclusion Criteria:

Subject with Duchenne muscular dystrophy eligible for enrolment in the study must meet all of the following criteria:

1. Has an out of frame deletion(s) that could be corrected by skipping exon 53 as confirmed by any of methodology at the time of visit 1. If not confirmed by any of methodology that evaluates the relative copy number of all exons (i.e. MLPA, CGH etc), must be confirmed through these techniques by the time of visit 4.
2. DNA sequencing of exon 53 confirms that no DNA polymorphisms occur that could compromise duplex formation between NS-065/NCNP-01 and pre-mRNA.
3. There is confirmation of detection of dystrophin mRNA with skipping of exon 53 and dystrophin production after in vitro exposure of NS-065/NCNP-01 to subject-derived cells.
4. Male and >= 5 years and < 18 years of age at the time of obtaining informed consent and/or assent.
5. Able to give informed consent in writing signed by parent(s) or legal guardian who is able to understand all of the study procedure requirements. If applicable, able to give informed assent in writing signed by the subject.
6. Life expectancy of at least 1 year
7. Unable to ambulate. Ambulant subject can be enrolled according to the circumstances.
8. Have intact muscles, which have adequate quality for biopsy. (No lacks or severe atrophy of tibialis anterior muscle)
9. QTc <450 msec (based on 12-lead ECGs), or <480 msec for subject with Bundle Branch Block.
10. If taking glucocorticosteroids, no significant change in total daily dosage or dosing regimen after the time of visit 1.

Exclusion Criteria:

Subject with Duchenne muscular dystrophy meeting any of the following criteria must not be enrolled in the study:

1. Has participated in other pharmacological clinical trial that might recover dystrophin protein by the readthrough or the exon-skipping therapy, and/or upregulate the dystrophin-associated proteins such as utrophin.
2. A forced vital capacity (FVC) < 50% of predicted.
3. A left ventricular ejection fraction (EF) < 40% or fractional shortening (FS) < 25% based on echocardiogram (ECHO).
4. Surgery within the last 3 months prior to the first anticipated administration of study medication or planned for anytime during the duration of the study.
5. Positive hepatitis B surface antigen (HbsAg), hepatitis C antibody test (HCV), or human immunodeficiency virus (HIV) test at screening.
6. Current diagnosis of any immune deficiency or autoimmune disease.
7. Current diagnosis of any active or uncontrolled infection, cardiomyopathy, or liver or renal disease.
8. Use of any other investigational agents and/or experimental agents within 3 months prior to the first anticipated administration of study medication.
9. History of any severe drug allergy.
10. Unable to give informed consent about using adequate contraception from the first administration until at least 6 months after the last dose of study medication, by parent(s) or legal guardian.

11. Subject considered by the investigator (or sub-investigator), for any reason, to be an unsuitable candidate for the study.

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Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: NS-065/NCNP-01	Drug: NS-065/NCNP-01; NS-065/NCNP-01 for Infusion is packaged as 25 mg/mL in phosphate buffered saline with 1 mL per vial. Study dosages will be infused over a 1 hour period with Normal saline as follows: Cohort 1: 1.25mg/kg once weekly for 12 weeks; Cohort 2: 5.0mg/kg once weekly for 12 weeks; Cohort 3: 20.0mg/kg once weekly for 12 weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Safety and tolerability (adverse event and adverse drug reaction)	Up to 15-17 weeks (12 weeks treatment period and 3-5 weeks follow up period)

Secondary Outcome Measures

Outcome Measure	Time Frame
Expression of dystrophin protein	At 14-15 weeks (2-3 week after from 12 weeks treatment period)
Detection of exon53 skipped mRNA of dystrophin	At 14-15 weeks (2-3 week after from 12 weeks treatment period)
NS-065/NCNP-01 concentration of the blood plasma	12 weeks
NS-065/NCNP-01 concentration of the urine	12 weeks
Serum Creatine kinase concentration	14 weeks

Collaborators and Investigators

• Sponsor: National Center of Neurology and Psychiatry, Japan
• Collaborators: Nippon Shinyaku Co., Ltd.
• Investigators: Study Director: Shin'ichi Takeda, MD, PhD, National Center of Neurology and Psychiatry; Principal Investigator: Hirofumi Komaki, MD, PhD, National Center of Neurology and Psychiatry

Study record dates

Study Major Dates

• Study Start: June 1, 2013
• Primary Completion (Actual): November 1, 2014
• Study Completion (Actual): August 1, 2015

Study Registration Dates

• First Submitted: March 5, 2014
• First Submitted That Met QC Criteria: March 5, 2014
• First Posted (Estimate): March 7, 2014

Study Record Updates

• Last Update Posted (Actual): February 26, 2020
• Last Update Submitted That Met QC Criteria: February 24, 2020
• Last Verified: February 1, 2020

More Information

Terms related to this study

• Keywords: Duchenne muscular dystrophy; NS-065/NCNP-01; exon 53 skipping; morpholino
• Additional Relevant MeSH Terms: Nervous System Diseases; Genetic Diseases, Inborn; Genetic Diseases, X-Linked; Musculoskeletal Diseases; Muscular Diseases; Neuromuscular Diseases; Muscular Disorders, Atrophic; Muscular Dystrophies; Muscular Dystrophy, Duchenne
• Other Study ID Numbers: NCNP/DMT01; UMIN000010964 (Other Identifier: UMIN-CTR)