Supernus Pharmaceuticals Inc (NASDAQ:SUPN) has entered into an agreement to acquire Biscayne Neurotherapeutics, a privately-held company developing a novel treatment for epilepsy, the pharmaceutical company revealed on Tuesday.
Supernus focuses on developing and commercialising products for the treatment of central nervous system (CNS) diseases. It will pay an initial sum of USD15m for Biscayne, plus further payments including USD73m, contingent on achieving certain development milestones, and up to USD95m contingent upon achieving certain sales milestones.
Additionally, Supernus will pay a low single-digit royalty on net sales to Biscayne and any applicable royalties to third parties for the use of in-licensed intellectual property (IP). The maximum combined royalty Supernus will pay to all parties is approximately 12%.
Through this acquisition Supernus will obtain worldwide rights (excluding certain markets in Asia where rights have been out-licensed) to Biscayne's product candidate which is in Phase I clinical development and has received an Orphan Drug designation from the US Food and Drug Administration (FDA) for the treatment of Dravet Syndrome, a severe form of childhood epilepsy. Supernus will also obtain rights to all the product candidate's underlying and related IP.
The transaction is expected to close in the next few weeks.
MaaT Pharma reveals positive 18-month data for MaaT013 in GI-aGvHD
Innate Pharma advances Sanofi-developed NK cell engager to Phase 2 for blood cancer patients
Precision Epigenomics partners with TruDiagnostic
Illumina's GRAIL divestment plan receives EC approval
Soligenix receives orphan drug designation from FDA for active ingredient in SuVax
Candel Therapeutics granted FDA Orphan Drug Designation for CAN-2409 in pancreatic cancer treatment
Lipogems completes patient enrolment in ARISE I US FDA IDE study
Amylyx Pharmaceuticals' AMX0035 shows promising impact on Wolfram syndrome symptoms
Ondine Biomedical's Steriwave approved for use by HCA UK
Roche attains CE Mark for first companion diagnostic for HER2-low metastatic breast cancer
Cadrenal Therapeutics' tecarfarin receives US FDA Orphan Drug Designation
BioCity Biopharma's BC2027 Phase one study IND application receives US FDA approval
Seres Therapeutics completes patient enrollment for SER-155 Phase 1B trial
Syros receives Fast Track Designation from FDA for tamibarotene in AML