Nektar Therapeutics (Nasdaq: NKTR), a biotechnology company focused on the discovery and development of novel therapies to treat autoimmune disorders, announced on Monday that it has signed a definitive agreement with Ampersand Capital Partners, a Boston-based private equity firm, to sell its Huntsville, Alabama manufacturing facility and reagent supply business.
Under the agreement, Ampersand will acquire Nektar's commercial-scale manufacturing facility and PEGylation reagent supply business for a total consideration of USD90m, which includes USD70m in cash proceeds and USD20m in a retained equity position for Nektar in a newly-created Ampersand portfolio company. Ampersand is also planning to invest additional growth equity capital in the new portfolio company. Following the closing of the deal, Nektar will be qualified to appoint a representative to the board of the new Ampersand portfolio company.
Nektar will retain all rights to current and future royalty streams and milestones related to existing PEGylated product licence agreements.
Subject to customary closing conditions and costs, the transaction is is expected to be completed by 2 December 2024.
Organon adds VTAMA cream to dermatology portfolio with acquisition of Dermavant
Redwire partners with Bristol Myers Squibb for space-based drug research
Accord Healthcare wins CHMP approval for Stelara biosimilar Imuldosa
Adicet Bio receives FDA clearance to expand ADI-001 trials to additional autoimmune diseases
Cantargia reports positive safety and biomarker results in CAN10 phase 1 trial
Lundbeck launches clinical trial for CD40L blocker Lu AG22515
Merck acquires CN201 from Curon Biopharmaceutical
Adicet Bio announces enrollment for Phase 1 trial to evaluate ADI-001 in autoimmune diseases
Alvotech launches confirmatory study for Entyvio biosimilar
Biocon BIologics unveils new dermatology data at EADV Congress 2024
Nektar Therapeutics showcases rezpegaldesleukin at EADV 2024
UCB and Biogen report positive Phase 3 results for dapirolizumab pegol in SLE
Priovant Therapeutics enrols first patients in brepocitinib CLARITY study
AstraZeneca's Fasenra recommended for EU approval in EGPA
Sareum Holdings secures patent allowance for SDC-1801 in China