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Truway Health HEAR-RESTORE exploratory inner-ear regenerative study
Also known as: Truway Health HEAR-RESTORE Regenerative Study, HEAR-RESTORE, TH-PRS-IEAR-2026-001, NCT07472023
Truway Health, Inc.
Company
Truway Health, Inc.
Program Type
Therapeutic
Modality
Regenerative Medicine
Stage
Phase 1
Status
Active
Target Gene
—
Route / Mode
Unspecified investigational regenerative interventions
Confidence
68%
Status Confidence
Status needs checking
Evidence Strength
Needs more support
Last Reviewed
2026-06-09
Geography
United States
Population
adult, tinnitus, sensorineural, noise-induced, sudden, regenerative-medicine
Trial IDs
1
Mechanism
Exploratory study describing broad investigational regenerative pharmacologic, stem-cell, and combination therapy concepts for inner-ear injury, tinnitus, and sensorineural hearing loss; specific product composition is not disclosed in the registry.
Indications
Notes
Verified only as a Truway-sponsored registry study record. ClinicalTrials.gov lists HEAR-RESTORE as enrolling by invitation, but the intervention descriptions are broad, product composition is unspecified, and completion dates extend to 2099. Present this as a low-confidence study-level record, not as a validated therapeutic product program.
Evidence & Sources
1 structured sourcesclinicaltrials
Supports: canonicalName, aliases, company, allCompanies, isIndustrySponsored, stage, status, indications...
IDs: NCT07472023, HEAR-RESTORE, TH-PRS-IEAR-2026-001
Key Events
Clinical Trials (1)
Data Checks
industry-sponsored-studybroad-unspecified-interventionsregistry-only-evidenceunusually-long-completion-dateverified-study-not-validated-product
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