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).
Carisma Therapeutics' CT-0525 IND application receives US FDA approval
Orexo's OX124 New Drug Application accepted for review by US Food and Drug Administration
GE HealthCare expands Critical Care Suite with FDA-cleared Pneumothorax detection algorithm
NanoVibronix initiates clinical study for UroShield at University of Michigan
Acrivon Therapeutics secures FDA Breakthrough Device designation for ACR-368 OncoSignature assay
Orexo's opioid overdose rescue medication, OX124, gains FDA acceptance for review
SpringWorks Therapeutics' Ogsiveo tablets receive US FDA approval
RedHill Biopharma granted five years' market exclusivity for Talicia by US FDA
Arcturus Therapeutics granted FDA Orphan Drug Designation for ARCT-032 to treat cystic fibrosis
Genelux secures FDA Fast Track designation for Olvi-Vec in ovarian cancer
EMA accepts Valneva's chikungunya vaccine application for accelerated assessment
Dupixent shows significant COPD exacerbation reduction in Phase 3 trial, accelerating FDA submission
Everest Medicines Nefecon receives Chinese regulatory approval