rAAVrh74.MHCK7.DYSF.DV for Treatment of Dysferlinopathies

Phase 1

Completed

• Conditions: Dysferlinopathy
• Interventions: Drug: rAAVrh74.MHCK7.DYSF.DV

• Registration Number: NCT02710500
• Lead Sponsor: Sarepta Therapeutics, Inc.

Brief Summary

The proposed clinical trial is a double-blind, randomized controlled study with direct intramuscular injection of rAAVrh.74.MHCK7.DYSF.DV gene vector to the extensor digitorum brevis muscle (EDB). Two cohorts of subjects with dysferlin deficiency, each with proven mutations will undergo gene transfer. A minimum of three subjects will be enrolled into each cohort.

Detailed Description

This is a phase I safety and tolerability study with a direct intramuscular injection of rAAVrh.74.MHCK7.DYSF.DV transferred to the extensor digitorum brevis muscle (EDB). The study is designed as a randomized, controlled, dose escalation trial with one EDB receiving the rAAVrh.74.MHCK7.DYSF.DV and the other side receiving saline alone. It will follow the previously safe and effective IM gene transfer to EDB for LGMD2D.2, 3 The first cohort, inclusive of three Dysferlinopathy subjects, will receive a gene transfer total dose of 2 x 10\^12 vector genomes. Muscle biopsies will be performed at Day 45 (two subjects) and Day 90 (one subject). If there are no safety concerns, three additional subjects will be enrolled and receive an escalated dose at 6 X 10\^12 vg (total dose). Muscle biopsies in the second cohort will be performed at Day 90 (one subject) and Day 180 (two subjects). This protocol design gives us a maximum period of observation ranging from 6 weeks to 6 months to capture both transient and delayed gene expression, and to recognize sustained expression.

Study Timeline

• Study First Submitted: 2016-02-11
• Study Start: 2016-03
• Study First Submitted QC: 2016-03-11
• Study First Posted: 2016-03-16
• Primary Completion: 2019-07
• Study Completion: 2019-07
• Status Verified: 2021-05
• Last Update Submitted: 2021-05-11
• Last Update Posted: 2021-05-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 2

Inclusion Criteria

• Must be Non-ambulant (cannot walk 10 meters in ≤ 30 sec) and age 18 years or older
• Established mutations of the dysferlin gene on both alleles
• Impaired muscle function but with sufficient muscle preservation to ensure muscle transfection based on magnetic resonance image of the EDB showing sufficient muscle preservation to permit transfection
• Willingness of sexually active subjects with reproductive capacity to practice reliable method of contraception (If appropriate), during the first six months after gene transfer (females) or until two negative sperm samples are obtained post gene transfer (males).

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Exclusion Criteria

• Active viral infection based on clinical observations or serological evidence of HIV, or Hepatitis A, B or C infection
• The presence of a Dysferlin mutations without weakness or loss of function
• Symptoms or signs of cardiomyopathy, including:
• Dyspnea on exertion, pedal edema, shortness of breath upon lying flat, or rales at the base of the lungs
• Echocardiogram with ejection fraction below 40%
• Diagnosis of (or ongoing treatment for) an autoimmune disease
• Persistent leukopenia or leukocytosis (WBC ≤ 3.5 K/µL or ≥ 20.0 K/µL) or an absolute neutrophil count < 1.5K/µL
• Concomitant illness or requirement for chronic drug treatment that in the opinion of the PI creates unnecessary risks for gene transfer
• Pregnancy
• AAVrh74 or AAV8 binding antibody titers > 1:50 as determined by ELISA immunoassay
• Abnormal laboratory values in the clinically significant range in the table below, based upon normal values in the Nationwide Children's Hospital Laboratory: GGT, Total Bilirubin, Cystatine, Hemoglobin, White Blood Cells

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Cohort 2 (High Dose)	rAAVrh74.MHCK7.DYSF.DV	Three (n=3) dysferlin deficiency subjects will receive bilateral injections with one extensor digitorum brevis muscle (EDB) receiving the rAAVrh74.MHCK7.DYSF.DV and the other side receiving saline alone.Subjects will receive a total dose of 6 x 10\^12 vg in one muscle. Intervention Drug: rAAVrh74.MHCK7.DYSF.DV
Cohort 1 (Low Dose)	rAAVrh74.MHCK7.DYSF.DV	Three (n=3) dysferlin deficiency subjects will receive bilateral injections with one extensor digitorum brevis muscle (EDB) receiving the rAAVrh74.MHCK7.DYSF.DV and the other side receiving saline alone.Subjects will receive a total dose of 2 x 10\^12 in one muscle. Intervention Drug: rAAVrh.MHCK7.DYSF.DV

Primary Outcome Measures

Name	Time	Method
Determination of safety based on the development of unacceptable toxicity	2 Years	Defined as the occurrence of any one Grade III or higher, unanticipated, treatment-related toxicity

Secondary Outcome Measures

Name	Time	Method
Number of participants showing dysferlin protein expression in muscle tissue	2 Years	More than 3 fold increase in dysferlin protein expression in muscle compared to control side by western blot or more than 30% increase in dysferlin-expressing fibers; Dysferlin protein expression as demonstrated with N -terminal anti-dysferlin antibodies will be quantified using BioQuant
Number of inflammatory cells in muscle	2 Years	Number of inflammatory cells per mm2 area
Leukocyte marker counts including CD45, CD3, CD4, CD8, and MAC 387.	2 Years	Number of CD4+ cells/ mm2 area; Number of CD8+ cells/ mm2 area; Number of muscle fibers expressing MHCI staining / mm2 area; Number of muscle fibers expressing MHCII staining / mm2 area
Binding antibodies counts and ELISpot counts to both rAAVrh74 capsid and dysferlin protein.	2 Years	AAVrh74 or AAV8 binding antibody titers \> 1:50 as determined by ELISA immunoassay

Trial Locations

Locations (1)

Nationwide Children's Hosptial; 🇺🇸 Columbus, Ohio, United States