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ClinicalTrials.gov 1 recruiting now early-phase tilt small index

Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF): early-phase trial registry

1 of 1 indexed Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) trials are currently recruiting, with more weight in Phase 1-2.

Corpus placement: #11,370 of 28,707 conditions by registered trial count.

1 US clinical trials · 1 currently recruiting · #11,370 of 28,707 conditions by registered trial count

Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF): 1 US clinical trial tracked, 1 recruiting.

Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) is the subject of 1 registered US clinical trials on ClinicalTrials.gov, 1 of them currently open to new participants. 0 are in Phase 3-4 (later-stage) and 1 in Phase 1-2 (earlier-stage). The most active sponsor is Regeneron Pharmaceuticals, running 1 of these trials.

Enrollment posture brief

Registry condition congenital-hearing-loss-secondary-to-biallelic-mutations-of-the-otoferlin-gene-o

OPEN 1 | RECR 100% | LATE 0 | EARLY 1 | RANK #11370 | SPON 1

Nearest open-share peer: Aortic Arch Aneurysm (100% recruiting · 5 trials)

Congenital Hearing Loss (th…100%Ablation80%ACL Reconstruction80%Abuse, Drug60%Acceptability60%
Open-enrollment share among volume-matched conditions near Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF)

Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) lists 1 open slots (100% of 1 indexed trials). Peers are matched on registered volume, not therapeutic-area browse lists. How peer matching works →

Key findings

What ClinicalTrials.gov does not surface for Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) on its own pages , computed from the registry mirror as of 2026-08-08. Each line carries its own denominator so it can be quoted as it stands.

  1. Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) is recruiting above its size-band peers.

    1 of 1 indexed trials (100%) are open to enrollment, against a 46.5% average across 27,806 conditions with fewer than 20 trials. The peer set uses the same ClinicalTrials.gov-derived counts as this page.

Phase 11

Phase Distribution

PhaseTrial count
Phase 1 1

Top Sponsors

Named interventions

Most-linked intervention names on Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) records (sponsor-reported on ClinicalTrials.gov). Counts are trial links, not unique products.

DB-OTO Genetic
1 trials

US sites by state

Facility locations filed on Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) trials. A trial with sites in several states counts in each.

Wisconsin 1 trials
Washington 1 trials
Ohio 1 trials
New York 1 trials
Massachusetts 1 trials
Florida 1 trials
California 1 trials

Source: ClinicalTrials.gov, National Library of Medicine. Data is informational only.

What to do with this Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) page

1 registered trials, 1 currently recruiting, is a starting point for a conversation, not a diagnosis or a recommendation.

  • 1 Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) trials are currently recruiting, check eligibility criteria before contacting a site. Browse recruiting trials
  • Regeneron Pharmaceuticals sponsors the most Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) trials on record, review their full trial history before evaluating a specific study. See Regeneron Pharmaceuticals's trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF) condition card totals 1 registered trials; most-linked intervention DB-OTO; top US site state Wisconsin. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.