A First-in-human Study of EPI-321 in Facioscapulohumeral Muscular Dystrophy

Last updated: May 8, 2025
Sponsor: Epicrispr Biotechnologies, Inc.
Overall Status: Active - Recruiting

Phase

1/2

Condition

Muscular Dystrophy

Treatment

EPI-321

Clinical Study ID

NCT06907875
EPI-321-02
  • Ages 18-75
  • All Genders

Study Summary

The goal of this clinical trial is to learn how safe and tolerable EPI-321 is and whether there may be early signs it is working in male or female adult (18 to 75 years) participants with facioscapulohumeral muscular dystrophy (FSHD) Type 1 condition. The main questions it aims to answer are:

How safe is EPI-321 and how well can people handle it over time? How does EPI-321 interact with its target and does it show early signs of working?

Participants will receive a single dose of EPI-321 through a vein while being closely watched in a hospital and visit the clinic regularly for tests and checkups for about 5 years after getting EPI-321.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Able and willing to provide informed consent

  • Male or female 18 to 75 years of age

  • Clinical diagnosis of FSHD with genetic Type 1

  • FSHD Ricci clinical severity score 2 to 4 (on 5-point scale)

  • Has adequate liver function

  • Has adequate kidney function

Exclusion

Exclusion Criteria:

  • Has an anti-AAVrh74 total binding antibody titer > 1:400

  • Requires a walker or wheelchair for ambulation

  • Pregnant and/or breastfeeding at baseline or is planning to become pregnant duringthe first 12 months following EPI-321 administration

  • Has FSHD Type 2

  • Has a body mass >90 kg

  • Has a concurrent or past medical conditions could jeopardize the safety of theparticipant

Study Design

Total Participants: 9
Treatment Group(s): 1
Primary Treatment: EPI-321
Phase: 1/2
Study Start date:
May 08, 2025
Estimated Completion Date:
April 30, 2032

Study Description

EPI-321 is an investigational drug product comprising a recombinant adeno-associated viral vector, serotype rh74 (AAVrh74), for the delivery of genetic material encoding an epigenetic editor designed to address the root case of FSHD. AAVrh74 has been shown to transduce human skeletal muscle efficiently in the clinical experience. EPI-321's transgene product, a non-cutting, nuclease-dead mini, clustered regularly interspaced short palindromic repeat (CRISPR)-associated protein (dCasONYX) with fuse epigenetic modulators, is designed to selectively bind the D4Z4 repeat region via the accompanying guide RNA, methylate CpG groups within the region near the DUX4 gene on chromosome 4q35, and thus repress the expression of toxic DUX4 protein, ameliorating the downstream pathology that drives FSHD. As it is under a muscle-specific promoter, the dCasONYX-fused protein is expected to be preferentially and actively expressed in muscle tissue following a single intravenous (IV) dose.

EPI-321-02 clinical trial is an open label dose ascending study of EPI-321 for safety and tolerability to determine the best dose for a future trial of drug activity. Two dose levels will be evaluated. In addition, this study will collect secondary outcome data on muscle function, imaging characteristics, and other markers of disease activity at the baseline and throughout the study to assess their utility as measures of drug activity in a future clinical trial.

Connect with a study center

  • Pacific Clinical Research Network

    Auckland, 0622
    New Zealand

    Site Not Available

  • Rare Disease Research

    Atlanta, Georgia 303329
    United States

    Active - Recruiting

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