MELT-300
Phase 2- Indications
- Anxiety, Pain
Company intelligence / Profile preview
Melt Pharmaceuticals recently reported positive topline efficacy results from a pivotal Phase 3 trial of its lead product candidate, MELT‑300, a non-IV, non-opioid sublingual tablet for procedural sedation in cataract surgery. The study met safety and efficacy endpoints under an FDA Special Protocol Assessment. The company plans to seek regulatory approval via the FDA’s 505(b)(2) pathway[6].
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