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SK Bio taps up Biohaven for Kv7 platform and epilepsy drug in USD 795m deal

SK Bio taps up Biohaven for Kv7 platform and epilepsy drug in USD 795m deal

SK Biopharmaceuticals has agreed to acquire an exclusive worldwide license to Biohaven Ltd.'s (NYSE: BHVN) Kv7 ion channel platform, including lead asset opakalim (BHV-7000), a selective Kv7.2/7.3 potassium channel activator in pivotal Phase II/III development for focal epilepsy, in a deal worth up to USD 795 million plus tiered royalties.

Under the terms, Biohaven receives USD 400 million in near-term cash — USD 350 million at closing and USD 50 million in 2027 — plus up to USD 150 million in development and regulatory milestones. SK also assumes up to USD 245 million in future Kv7 program costs, including milestone and royalty obligations owed to Knopp Biosciences, the platform's originator. Biohaven retains tiered royalties on US net sales ranging from the mid-teens to low twenties percent. The license covers the full Kv7 discovery platform and all related compounds, not solely opakalim.

Biohaven completed enrollment in the RISE3 Phase II/III focal epilepsy study on June 30, 2026, with topline results expected in the second half of this year. SK is paying USD 350 million at closing without seeing those results, betting on the clinical signals accumulated across more than 1,200 participants to date. Opakalim is described by the company as differentiated from earlier Kv7 activators by its selectivity for Kv7.2/7.3 heteromeric channels, which Biohaven attributes to the compound's reported low rates of somnolence, dizziness, and fatigue in clinical studies. In May 2026, Biohaven reported clinical data showing seizure control alongside a tolerability profile the company characterized as markedly differentiated.

Through its US subsidiary SK Life Science, the South Korea-based company markets cenobamate (Xcopri) for partial-onset seizures in adults, with a dedicated neurology field force of more than 150 professionals. SK targets a US commercial launch for opakalim as early as 2029, according to its own announcement of the deal. The company describes opakalim as the second innovative drug it plans to launch directly in the US.

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The company acquired the Kv7 platform from Knopp Biosciences in 2022, advanced it through pivotal trials, and is now out-licensing before a binary data readout. The USD 400 million upfront Biohaven commands now compares with the USD 100 million in initial consideration Biohaven agreed to pay Knopp. The USD 350 million at closing provides immediate non-dilutive capital as Biohaven simultaneously advances a Phase III trial of its MoDE extracellular protein degrader BHV-1300 in Graves' disease, a Phase II/III Parkinson's program, and an FGFR3-directed antibody-drug conjugate with early ESMO data.

Xenon Pharmaceuticals' azetukalner, also a Kv7.2/7.3 opener in Phase III for focal onset seizures, has reported positive topline data from its X-TOLE2 study and the company has indicated plans to submit a new drug application to the US FDA in Q3 2026. If approved before opakalim completes its regulatory pathway, azetukalner would establish the class standard in the market SK is entering. Closing of the Biohaven-SK agreement remains subject to Hart-Scott-Rodino (HSR) Antitrust Improvements Act review and other customary conditions.


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