NVK029
Presbyopia
Phase 2Active
Key Facts
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.
View full company profileTherapeutic Areas
Other Presbyopia Drugs
| Drug | Company | Phase |
|---|---|---|
| Presbyopia Treatment | Viatris (2) | NDA Submitted |
| Presbyopia-Correcting ICL | STAAR Surgical | Research & Development |
| LB-01 | Lento Bio | Discovery/IND-Enabling |
| LB-02 | Lento Bio | Discovery |
| Presbyopia-Correcting Contact Lenses | Clerio Vision | Development |
| Intra-corneal Implant | MAG Optics | Pre-clinical |
| ArtiPlus | Ophtec | Clinical Trials |
| BRIMOCHOL™ PF | Tenpoint Therapeutics | NDA Submitted |
| Qlosi™ | Orasis Pharmaceuticals | Approved |
| TSH‑001 | TSH Biopharm | Phase 1/2 |
| DE-128A | Santen Pharmaceutical | Phase 2 |
| YP-10 | Viatris | NDA Filed |