Skip to content
MedsAcross

Molecule

Lunsotogene parvec

Available on requestBiologicCold chain
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Lunsotogene parvec is a prescription medicine. It is available as injection for intracochlear use. MedsAcross supplies Lunsotogene parvec for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

US FDA first approval
Not recorded
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intracochlear
Dosage forms
Injection
Biologic
Yes
Identifiers
UNII P6ZNU67HPU

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

OTARMENI is indicated for the treatment of pediatric and adult patients with severe-to-profound and profound sensorineural hearing loss (any frequency >90 dB HL) associated with molecularly confirmed biallelic variants in the OTOF gene, preserved outer hair cell function, and no prior cochlear implant in the same ear. This indication is approved under accelerated approval based on the improvement of hearing sensitivity assessed by average pure tone audiometry (PTA) at Week 24. Continued approval for this indication may be contingent upon verification and description of clinical benefit in the confirmatory clinical trial.

Source: US FDA prescribing information

How it works

Intracochlear infusion of OTARMENI results in expression of the OTOF gene primarily in inner hair cells (IHCs), which facilitates production of functional otoferlin protein and restores synaptic transmission to the auditory nerve as shown in animal studies in mice.

Source: US FDA prescribing information

Dosing overview

For intracochlear infusion only. Recommended dose of OTARMENI for each ear is 7.2 × 10 12 vector genomes (vg) in a total volume of 0.24 mL, administered by a single-dose intracochlear infusion.

Source: US FDA prescribing information

Warnings and precautions

Procedure-Related Risks: Monitor patients for procedure-related adverse reactions with OTARMENI administration. Procedure-Related Risks Procedure-related adverse reactions may occur with OTARMENI administration including vertigo, tinnitus, cerebral spinal fluid leak, ipsilateral facial paresis, ipsilateral change in taste, meningitis, wound infection, mastoiditis, numbness around the ear, blood or fluid collection at surgical site, and labyrinthitis. Monitor patients for procedure-related adverse reactions with OTARMENI administration and manage accordingly.

Source: US FDA prescribing information

Side effects

The most common adverse reactions (incidence ≥5%) include otitis media, vomiting, nausea, dizziness, procedural pain, gait disturbance, and nystagmus.

Source: US FDA prescribing information

Storage

Store and transport OTARMENI (package 1) frozen at -80°C (-112°F). Thaw OTARMENI at room temperature prior to administration. If not used immediately, the unpunctured thawed vial can be stored in the refrigerator (2°C to 8°C [36°F to 46°F]) for up to 24 hours or at room temperature (up to 25°C [77°F]) for up to 8 hours. Administration Kit for use with OTARMENI: Store at room temperature in original carton separately from OTARMENI until time of use. Do not freeze.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

1 presentations of Lunsotogene parvec, sorted by availability.

MedicineManufacturerRegisterAvailability
Otarmeni 30000000000000 GC/mL injectionIntracochlear Cold chainRegeneron PharmaceuticalsUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDANot recorded—
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Lunsotogene parvec available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Lunsotogene parvec and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Lunsotogene parvec have?

The catalogue lists 1 brand names for Lunsotogene parvec, including Otarmeni.

Does Lunsotogene parvec need cold chain shipping?

At least one listed presentation of Lunsotogene parvec must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

References

  1. OTARMENI prescribing information (Regeneron Pharmaceuticals). U.S. National Library of Medicine, DailyMed. Retrieved 27 April 2026

Request Lunsotogene parvec for export supply

Tell us the strength, quantity and destination country. Our team replies with availability, lead time and the import documents needed.