RNA-based therapeutics developer Altamira Therapeutics Ltd (Nasdaq:CYTO) on Friday unveiled plans for a partial spin-off of its subsidiary Altamira Medica AG, in line with a strategic shift towards its core RNA delivery technology.
Altamira has entered into a binding agreement for the sale of a 51% stake in Medica to a Swiss private equity investor. Medica will continue operating under its current name and with current staff in collaboration with Altamira.
Medica's key asset is Bentrio, a drug-free over-the-counter nasal spray used for the treatment of allergic rhinitis, which has been cleared by the FDA and is being commercialised in several markets.
The transaction, valued at CHF2.04m (approximately USD2.3m) in cash, leaves Altamira with a 49% share in Medica and a 25% entitlement to Medica's future licensing income. Additionally, the deal includes the sale of Auris Medical Pty Ltd in Australia and a pro-rata cash contribution of CHF1m to Medica's capital by its two shareholders.
Set to close on 21 November 2023, subject to customary conditions, the transaction is expected to yield a financial gain of around USD5.2m for Altamira under International Financial Reporting Standards (IFRS).
Correction - DeepHealth expands FDA clearance for SmartMammo Dx with GE HealthCare integration
DeepHealth expands FDA clearance for SmartMammo Dx with GE HealthCare integration
Formosa Pharmaceuticals licenses eye drops for Switzerland and Liechtenstein
Galderma reports Phase III data for nemolizumab in prurigo nodularis published in JAMA Dermatology
AOP Health's Rapiblyk approved by FDA for atrial fibrillation and atrial flutter
PTC Therapeutics to sell Priority Review Voucher for USD150m
Novartis' Kisqali approved in EU for broader population of high-risk early breast cancer patients
Merck reports positive Phase 3 ZENITH results for WINREVAIR in PAH treatment
Alnylam's sNDA for vutrisiran accepted by FDA; PDUFA date set for March 2025
GSK plc announces US FDA acceptance of review for Blenrep combinations in multiple myeloma
Hanmi Pharmaceutical and Beijing Hanmi Pharmaceutical announce progress in BH3120 clinical trial
Johnson & Johnson seeks FDA approval for subcutaneous TREMFYA