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NCT05973630 · ClinicalTrials.gov registry record · Phase 1

ATA-200 Gene Therapy Trial in Patients With LGMDR5

A Phase 1 study of LGMD2C, sponsored by Atamyo Therapeutics.

Active
Registry status
Phase 1
Development phase
4
Enrollment target
1
Study location

NCT05973630: Active Phase 1 study of LGMD2C, sponsored by Atamyo Therapeutics.

NCT05973630 is a Phase 1 study of LGMD2C that is active but no longer recruiting, run by Atamyo Therapeutics. The registered enrollment target is 4 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05973630, a Phase 1 study of LGMD2C, is active but no longer recruiting, sponsored by Atamyo Therapeutics.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
4 participants
Enrollment target
1
Study location

Study Summary

The purpose of ATA-003-GSAR study is to evaluate the safety and tolerability of a single intravenous infusion of ATA-200 in pediatric patients with limb girdle muscular dystrophy type 2c/R5 (LGMD R5).

Primary Outcome

Collection of adverse events at each visit

Conditions Studied

Interventions

  • BIOLOGICAL ATA-200

Study Locations (1)

Florida

  • Child Health Research Institute - Gainsville

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2025-02-15
Est. Completion 2031-01-31
Phase Phase 1
Atamyo Therapeutics

1 total trials

What the registry record for NCT05973630 still lists

NCT05973630 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower).

The record links to 1 condition, with LGMD2C appearing as the primary indexed condition, and to 1 intervention - of which ATA-200 is the first listed.

NCT05973630 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT05973630 about?

NCT05973630 is a clinical study titled "ATA-200 Gene Therapy Trial in Patients With LGMDR5". The purpose of ATA-003-GSAR study is to evaluate the safety and tolerability of a single intravenous infusion of ATA-200 in pediatric patients with limb girdle muscular dystrophy type 2c/R5 (LGMD R5).

What is the current status of trial NCT05973630?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2025-02-15. Estimated completion is 2031-01-31.

What conditions does trial NCT05973630 study?

This clinical trial studies the following conditions: LGMD2C.

What interventions are being tested in trial NCT05973630?

The interventions under investigation include: ATA-200 (BIOLOGICAL).

Who is sponsoring clinical trial NCT05973630?

This trial is sponsored by Atamyo Therapeutics, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05973630 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for LGMD2C

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05973630's enrollment target sits among peer trials

4 1995th of 2000 higher than 2 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05973630, the US trial registry maintained by the National Library of Medicine. NCT05973630 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.