Ketamine ANDA
PharmaTher's FDA-approved ketamine ANDA, sold in December 2025, has the potential to generate more than US$25 million over time, subject to commercial performance, with payments expected to begin in Q1 2027.
Available to license, sell, partner or spin out
Four assets ready for the right partner.
KetaVault™
CMC package, INDs, protocols and five orphan designations.
Ketamine microneedle patch
IND-enabling study complete; Phase 1-ready.
KetaMist® collaboration
Needle-free, patient-controlled ketamine; collaboration signed July 2026 toward an FDA pathway.
Sairiyo Therapeutics Inc.
PharmaTher's 49% interest in a company developing oral cepharanthine.
Request a non-confidential summary
Business development and licensing teams can request a summary of any asset.
Request a summaryInvestors
The corporate presentation covers every asset and its potential value.
Download the deck (PDF)Potential ANDA payments depend on the purchaser's commercial performance and are not assured. The licensing, sale, partnering or spin-out of strategic assets may not occur on acceptable terms. KetaMist® is a trademark of its owner. Forward-looking information; see Forward-looking statements.
