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NVK029

Presbyopia

Phase 2Active

Key Facts

Indication
Presbyopia
Phase
Phase 2
Status
Active
Company

About Vyluma

Vyluma is a clinical-stage biotech founded in 2020, headquartered in Bridgewater, New Jersey. Its lead candidate, NVK002, is a low-dose atropine eye drop in late-stage development to slow the progression of pediatric myopia, positioning it to potentially be the first FDA-approved pharmaceutical treatment for this condition. The company has a broader pipeline targeting other prevalent vision disorders like presbyopia and night vision disturbance, leveraging its expertise in topical ophthalmic formulations. Vyluma operates as a private, pre-revenue company aiming to transform the standard of care in ophthalmology.

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Other Presbyopia Drugs

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Presbyopia-Correcting ICLSTAAR SurgicalResearch & Development
LB-01Lento BioDiscovery/IND-Enabling
LB-02Lento BioDiscovery
Presbyopia-Correcting Contact LensesClerio VisionDevelopment
Intra-corneal ImplantMAG OpticsPre-clinical
ArtiPlusOphtecClinical Trials
BRIMOCHOL™ PFTenpoint TherapeuticsNDA Submitted
Qlosi™Orasis PharmaceuticalsApproved
TSH‑001TSH BiopharmPhase 1/2
DE-128ASanten PharmaceuticalPhase 2
YP-10ViatrisNDA Filed