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Biohaven and SK Biopharmaceuticals Enter into Strategic Global Licensing Agreement for Novel Kv7 Ion Channel Platform and Opakalim, Lead Candidate for Epilepsy

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Biohaven (NYSE: BHVN) and SK Biopharmaceuticals signed a strategic global licensing and collaboration agreement granting SK Biopharmaceuticals an exclusive worldwide license to Biohaven's Kv7 ion channel platform, led by opakalim (BHV-7000), a selective Kv7.2/7.3 activator in Phase 2/3 development for focal epilepsy.

According to Biohaven, the deal includes up to $795 million in upfront and milestone payments related to the Kv7 platform, $400 million in near-term cash ($350 million at closing and $50 million in 2027), and an additional $150 million in development and regulatory milestones, plus tiered royalties on global net sales of opakalim. SK Biopharmaceuticals will assume future Kv7 program costs, including up to $245 million of specified obligations to Knopp Biosciences, while leveraging its established epilepsy commercial infrastructure. Closing is subject to antitrust and other customary regulatory reviews.

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Positive

  • $400 million near-term non-dilutive cash to Biohaven ($350 million at closing, $50 million in 2027)
  • Total potential Kv7-related payments up to $795 million plus $150 million in additional milestones
  • Tiered U.S. opakalim royalties to Biohaven in the mid-teens to low twenties percentage range
  • SK Biopharmaceuticals assumes up to $245 million in specified Knopp and future Kv7 milestone obligations
  • SK Biopharmaceuticals funds Kv7 program costs going forward, reducing Biohaven’s development spend
  • Partnership leverages SK Biopharmaceuticals’ established epilepsy commercial platform, including XCOPRI experience

Negative

  • Biohaven grants SK Biopharmaceuticals an exclusive worldwide license to its Kv7 ion channel platform, including opakalim
  • Closing of the agreement is contingent on regulatory and antitrust reviews and other customary conditions
  • Opakalim remains in Phase 2/3 development, so clinical and regulatory success is still required before commercialization

News Explained

The royalty economics are geographic: Biohaven is to receive tiered royalties ranging from the mid-teens to low twenties on U.S. net sales of opakalim and a mid-single-digit royalty on sales outside the U.S.

Market Context

An effective S-3ASR dated May 4, 2026, remains on record for BHVN. Against the agreement's non-dilut...
Analysis

An effective S-3ASR dated May 4, 2026, remains on record for BHVN. Against the agreement's non-dilutive structure, that shelf is relevant financing context; closing remains contingent on regulatory and antitrust review.

Key Figures

Upfront and milestone payments: up to $795 million U.S. royalties: mid-teens to low twenties Cash consideration: $400 million +5 more
8 metrics
Upfront and milestone payments up to $795 million Kv7 platform agreement
U.S. royalties mid-teens to low twenties U.S. net sales of opakalim
Cash consideration $400 million $350 million at closing and $50 million in 2027
Closing payment $350 million payable at transaction closing
2027 payment $50 million additional cash consideration payable in 2027
Development and regulatory milestones $150 million additional payments to Biohaven
Assumed Kv7 obligations $245 million specified Knopp Biosciences and future Kv7 obligations
Participants studied more than 1,200 participants opakalim across multiple clinical trials

Historical Context

5 past events · Latest: Aug 10 (Neutral)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Aug 10 2Q26 earnings report Neutral -0.3% Quarterly results and pipeline updates were followed by a 0.34% decline.
Aug 06 Board appointment Positive +5.8% Technology investor joined the board, followed by a 5.8% gain.
Jul 27 Jury verdict Positive +1.3% Federal jury awarded Biohaven and Yale $4 million in damages.
Jul 20 Clinical data Positive -3.8% Early BHV-1530 data and a Regeneron supply agreement preceded a 3.76% decline.
Jul 09 Leadership transition Neutral -7.4% Scientific leadership changes were followed by a 7.39% decline.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

BHVN's recent positive announcements produced mixed reactions, with two aligned gains and three divergent declines or losses.

Key Terms

kv7.2/7.3 potassium channel activator, tiered royalties, non-dilutive capital, nda submission, +1 more
5 terms
kv7.2/7.3 potassium channel activator technical
"a next-generation, selective Kv7.2/7.3 potassium channel activator"
A Kv7.2/7.3 potassium channel activator is a drug or molecule that increases the opening or effectiveness of specific nerve cell ion channels made from Kv7.2 and Kv7.3 proteins, which help limit neurons' electrical firing. By acting like a dimmer switch that calms excessive nerve activity, these compounds are relevant to investors because their clinical progress, safety, and regulatory approval can affect the commercial value of companies developing treatments for epilepsy, neuropathic pain and other nervous-system disorders.
tiered royalties financial
"plus tiered royalties to Biohaven ranging from the mid-teens"
Tiered royalties are a payment structure where the percentage of earnings paid as royalties changes based on different levels of sales or production. For example, a company might pay a smaller percentage on initial sales and a higher percentage as sales increase beyond certain points. This system encourages higher sales by adjusting payments, making it important for investors to understand how revenue sharing may vary as a product or project grows.
non-dilutive capital financial
"The transaction delivers non-dilutive capital"
Funding that does not require a company to issue new shares or reduce existing owners’ percentage of ownership, such as grants, certain loans, licensing deals, or customer prepayments. It matters to investors because it preserves each shareholder’s stake and per-share value—like getting a loan or a gift instead of selling part of the company—while still carrying obligations (repayment, milestones, or restrictions) that can affect future cash flow and growth.
nda submission regulatory
"through NDA submission and beyond"
An NDA submission is the formal application a drug developer files with a medicines regulator seeking permission to market a new prescription drug. Think of it as the final product pitch that compiles all clinical trial results, safety data and manufacturing details so the regulator can decide whether the drug can be sold. For investors, an NDA submission is a major milestone because acceptance or approval can unlock sales and revenue, while delays or rejections create uncertainty and financial risk.
open-label extension study medical
"along with an open-label extension study"
An open-label extension study is a follow-on clinical trial where participants continue receiving a treatment and both patients and researchers know what is being given (no blind or placebo). It gathers longer-term safety, tolerability and effectiveness information beyond the initial trial, like turning a short test drive into a longer lease to see how the product performs over time. Investors watch these studies for evidence that a treatment is safe and durable, which can affect regulatory approval, market adoption and sales forecasts.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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  • SK Biopharmaceuticals to provide upfront and milestone payments related to the Kv7 platform up to $795 million, along with tiered royalties to Biohaven ranging from the mid-teens to low twenties on U.S. net sales of opakalim.

  • Opakalim, the lead candidate from Biohaven's Kv7 platform, is a next-generation, selective Kv7.2/7.3 potassium channel activator currently in Phase 2/3 development for focal epilepsy, with topline results from the RISE3 trial expected in 2H 2026. It is designed to offer an easy-to-use, once-daily oral treatment without the need for titration and a low incidence of burdensome CNS side effects.

  • The agreement pairs Biohaven's innovative, wholly owned Kv7 platform with the proven epilepsy commercial platform of SK Biopharmaceuticals, the team that launched XCOPRI®.  The deal gives opakalim an established path to patients worldwide through SK Biopharmaceuticals' commercial capabilities without Biohaven building its own capital-intensive infrastructure.

  • The transaction delivers non-dilutive capital, while retaining meaningful long-term upside in opakalim through milestones and royalties, materially strengthening Biohaven's balance sheet and extending its runway to advance a differentiated pipeline.

NEW HAVEN, Conn. and SEOUL, South Korea, Aug. 26, 2026 /PRNewswire/ -- Biohaven Ltd. and/or its wholly owned subsidiaries ("Biohaven") (NYSE: BHVN) and SK Biopharmaceuticals Co., Ltd. ("SK Biopharmaceuticals") today announced a strategic global licensing and collaboration agreement under which SK Biopharmaceuticals will obtain an exclusive worldwide license to Biohaven's Kv7 ion channel platform, led by opakalim (BHV-7000), a next-generation, selective Kv7.2/7.3 potassium channel activator in Phase 2/3 development for focal epilepsy, with RISE3 trial topline results expected in 2H 2026. Following the close of the transaction, the companies will collaborate to advance opakalim through development and U.S. Food and Drug Administration (FDA) approval, combining Biohaven's innovative Kv7 platform with SK Biopharmaceuticals' global development and regulatory capabilities and its proven commercial track record of bringing antiseizure medicines to patients worldwide.

SK biopharmaceuticals

Vlad Coric, M.D., Chairman and Chief Executive Officer of Biohaven, commented, "This is a landmark partnership that has the potential to deliver a novel treatment for millions of patients with epilepsy who still need better seizure control without exacerbating CNS adverse effects. Opakalim is one of the most exciting assets we have advanced; a selective Kv7.2/7.3 activator designed to deliver meaningful efficacy without the burdensome central nervous system side effects, including sedation and dizziness, associated with so many antiseizure medicines. SK Biopharmaceuticals is an ideal partner having launched XCOPRI and is the only company to bring a new antiseizure medicine for partial-onset (focal) seizures to patients in the U.S. since 2016. Pairing our scientific innovation with SK Biopharmaceuticals' established epilepsy development and commercialization expertise gives opakalim, if approved, its fastest and strongest path to patients worldwide. This partnership also brings $400 million in near-term, non-dilutive capital to Biohaven while preserving substantial long-term upside for our shareholders."

Under the terms of the agreement, SK Biopharmaceuticals to make upfront and milestone payments up to $795 million related to the Kv7 platform plus tiered royalties to Biohaven ranging from the mid-teens to low twenties on U.S. net sales of opakalim. Biohaven will receive $400 million in cash consideration, consisting of $350 million payable at closing and an additional $50 million payable in 2027, and Biohaven is eligible to receive an additional $150 million in development and regulatory milestone payments plus royalties on global net sales of opakalim. In addition, SK Biopharmaceuticals will assume responsibility for Kv7 program costs going forward under the terms of the agreement, including certain specified Knopp Biosciences and Kv7 future milestone obligations totaling $245 million and mid-single digit royalty obligations to Knopp Biosciences.

Donghoon Lee, President and Chief Executive Officer of SK Biopharmaceuticals, commented, "Our experience building XCOPRI into a therapy for epilepsy patients worldwide, from clinical development through global commercialization, has given us a deep understanding of what it takes to bring a differentiated CNS medicine to patients. We see opakalim as a highly complementary addition to our epilepsy portfolio, with a mechanism and tolerability profile that could extend our ability to serve patients who may benefit from additional treatment options. We look forward to a close, collaborative partnership with the Biohaven team through NDA submission and beyond."

With a history of more than 30 years, SK Biopharmaceuticals is the first global biopharmaceutical company in more than a decade, as well as the first Korean company, to independently discover, develop, and commercialize a novel antiseizure medicine. Through its U.S. subsidiary SK Life Science, Inc., the company markets XCOPRI® (cenobamate) for partial-onset (focal) seizures in adults in the U.S., where it has built a dedicated epilepsy commercial organization with a purpose-built neurology field force of over 150 professionals and established epilepsy-center and neurologist coverage. That mature infrastructure, paired with SK Biopharmaceuticals' global development, regulatory, and commercialization capabilities, has led to the steady, double-digit growth of XCOPRI and expanded its reach to patients worldwide.

Dr. Coric added, "Beyond opakalim, this transaction validates Biohaven's strategy of building differentiated, novel platforms that create value for patients and investors while pursuing monetization pathways beyond typical public-market equity raises. With such a robust pipeline, Biohaven has the potential to create value in numerous ways, including an outright sale, license agreements and partnerships with companies looking to expand their clinical-stage pipelines. Rather than stand up a commercial organization of our own for opakalim, we structured a partnership with a leading strategic partner in epilepsy to drive long-term revenue potential of this novel mechanism. This structure allows Biohaven to receive an upfront payment for our development efforts while sharing in future upside of opakalim through milestones and royalties. A strengthened balance sheet, coupled with a meaningfully lower go-forward burn and a world-class partner, lets us sharpen our focus and invest in the next wave of Biohaven innovation, from our MoDE and TRAP extracellular protein degraders in immunology to our programs in neuroscience, metabolic conditions, and rare diseases. We are building a diversified, self-sustaining engine for long-term value creation."

Summary of Financial Terms

  • Near-Term Cash Consideration to Biohaven: $400 million$350 million payable at closing and $50 million payable in 2027
  • Development and Regulatory Milestones to Biohaven: $150 million
  • U.S. Royalties: Tiered royalties on U.S. net sales of opakalim ranging from the mid-teens to low twenties
  • Ex-U.S. Royalties: Mid-single digit royalty on net sales of opakalim outside the U.S.
  • Assumption of Knopp and Future Kv7 Obligations: SK Biopharmaceuticals will assume certain specified Biohaven obligations, including upto $185 million payable to Knopp Biosciences upon U.S and EU approval, plus a mid-single digit worldwide royalty — separate from, and in addition to, SK Biopharmaceuticals' milestone and royalty obligations to Biohaven. SK Biopharmaceuticals will also assume up to $60 million in additional obligations for milestones related to future Kv7 pipeline programs.

All figures are expressed in U.S. dollars. Closing of the licensing and collaboration agreement is contingent on completion of review under applicable regulatory and antitrust laws, including the Hart-Scott-Rodino (HSR) Antitrust Improvements Act of 1976 in the U.S., and other customary closing conditions.

Advisors

J.P. Morgan Securities LLC is serving as exclusive financial advisor and Sullivan & Cromwell LLP is serving as legal advisor to Biohaven. Nomura Securities International, Inc. is serving as exclusive financial advisor and Paul Hastings LLP is serving as legal counsel to SK Biopharmaceuticals.

About Opakalim and Biohaven's Kv7 Ion Channel Platform

The lead asset in Biohaven's Kv7 platform is opakalim (BHV-7000), a next-generation, selective Kv7.2/7.3 potassium channel activator targeting a clinically validated mechanism of action for the treatment of epilepsy. Opakalim is differentiated from both first- and second-generation Kv7 activators by its selectivity for the Kv7.2/7.3 heteromeric channels that are the predominant regulators of neuronal excitability, with substantially less activity at GABA receptors. This selectivity profile is hypothesized to contribute to opakalim's favorable tolerability, including the low rates of somnolence, dizziness, and fatigue observed in clinical studies to date. Opakalim has been studied in more than 1,200 participants across multiple clinical trials. Biohaven is currently conducting two Phase 2/3 randomized, double-blind, placebo-controlled studies (NCT06132893 and NCT06309966) evaluating opakalim versus placebo as adjunctive therapy for refractory focal onset epilepsy, along with an open-label extension study (NCT06443463) assessing long-term efficacy and safety.

About Biohaven

Biohaven Ltd. (NYSE: BHVN) is a biopharmaceutical company focused on the discovery, development, and commercialization of life-changing treatments across immunology, neuroscience, and oncology. Biohaven is advancing an innovative portfolio of therapeutics built on proven drug development experience and multiple proprietary platforms, including Kv7 ion channel modulation for epilepsy; MoDE™ and TRAP™ extracellular protein degradation for immunological diseases; and myostatin inhibition for neuromuscular and metabolic diseases, including obesity. For more information, visit www.biohaven.com.

About SK Biopharmaceuticals

SK Biopharmaceuticals Co., Ltd., together with its U.S. subsidiary SK Life Science, Inc., is a global biopharmaceutical company focused on the discovery, development, and commercialization of treatments for central nervous system disorders. The company independently developed and commercializes XCOPRI (cenobamate) for the treatment of partial-onset seizures in adults, and continues to build a global pipeline spanning CNS disorders and oncology. For more information, visit https://www.skbp.com/eng.do.

Forward-Looking Statements

This news release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The use of certain words, including "will," "believe," "may," "expect," "on track," "potential," and similar expressions, is intended to identify forward-looking statements. Investors are cautioned that any forward-looking statements, including statements regarding the expected timing, conduct, and outcomes of Biohaven's ongoing and planned clinical trials of opakalim; the potential therapeutic benefits, efficacy, safety, and tolerability of opakalim; the anticipated closing of the transaction and satisfaction of closing conditions; the ability to achieve milestones and earn royalties; and the timing of planned regulatory interactions and filings, are not guarantees of future performance and involve substantial risks and uncertainties. Actual results, developments, and events may differ materially from those in the forward-looking statements as a result of various factors, including: the expected timing, commencement, and outcomes of Biohaven's planned and ongoing clinical trials; the timing of planned interactions and filings with the FDA; the timing and outcome of expected regulatory filings; complying with applicable U.S. regulatory requirements; the potential commercialization of Biohaven's product candidates; the cost of Biohaven's development and commercialization initiatives; and the effectiveness and safety of Biohaven's product candidates. Additional important factors are described in Biohaven's filings with the Securities and Exchange Commission, including under "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations." The forward-looking statements are made as of the date of this news release, and Biohaven does not undertake any obligation to update them, whether as a result of new information, future events, or otherwise, except as required by law.

XCOPRI is a registered trademark of SK Biopharmaceuticals Co., Ltd.

MoDE and TRAP are trademarks of Biohaven Therapeutics Ltd.

Contacts

Biohaven Investor Contact:
Jennifer Porcelli, Vice President, Investor Relations
jennifer.porcelli@biohavenpharma.com |  +1 (201) 248-0741

Biohaven Media Contact:
Mike Beyer, Sam Brown Healthcare Communications
mikebeyer@sambrown.com |  +1 (312) 961-2502

SK Biopharmaceuticals Media Contact:
Soohui Lim, Head of Public Relations
siri@skbp.com

 

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SOURCE Biohaven Ltd.

FAQ

What is the Biohaven (BHVN) and SK Biopharmaceuticals global licensing agreement announced on August 26, 2026?

The agreement grants SK Biopharmaceuticals an exclusive worldwide license to Biohaven’s Kv7 ion channel platform, led by opakalim. According to Biohaven, the companies will jointly advance opakalim through development and FDA approval, combining Biohaven’s Kv7 expertise with SK Biopharmaceuticals’ global development and epilepsy commercialization capabilities.

How much cash will Biohaven (BHVN) receive from the SK Biopharmaceuticals Kv7 licensing deal?

Biohaven expects $400 million in near-term cash, including $350 million at closing and $50 million in 2027. According to Biohaven, total potential payments tied to the Kv7 platform reach up to $795 million, plus $150 million in additional development and regulatory milestone payments.

What royalty rates will Biohaven (BHVN) earn on opakalim sales under the SK Biopharmaceuticals deal?

Biohaven will receive tiered U.S. royalties on net sales of opakalim ranging from the mid-teens to low twenties percentage range. According to Biohaven, it will also earn a mid-single digit royalty on net sales of opakalim outside the U.S., providing ongoing revenue participation.

What stage of development is opakalim (BHV-7000) in, and when are RISE3 trial results expected?

Opakalim is in Phase 2/3 development for focal epilepsy, being evaluated in randomized, double-blind, placebo-controlled studies. According to Biohaven, topline results from the RISE3 trial are expected in the second half of 2026, with an open-label extension assessing long-term safety and efficacy.

What obligations will SK Biopharmaceuticals assume in the Biohaven (BHVN) Kv7 licensing agreement?

SK Biopharmaceuticals will assume Kv7 program costs and specified Biohaven obligations totaling up to $245 million to Knopp and future Kv7 milestones. According to Biohaven, this includes up to $185 million upon U.S. and EU approvals and up to $60 million for future Kv7 pipeline milestones.

How might the SK Biopharmaceuticals partnership impact Biohaven’s (BHVN) balance sheet and cash runway?

The deal provides $400 million in near-term, non-dilutive capital and shifts future Kv7 costs to SK Biopharmaceuticals. According to Biohaven, these terms materially strengthen its balance sheet, extend its runway, and lower burn while preserving upside through milestones and royalties on opakalim.

What conditions must be met before the Biohaven (BHVN) and SK Biopharmaceuticals Kv7 deal closes?

Closing is contingent on completion of reviews under applicable regulatory and antitrust laws, including the U.S. Hart-Scott-Rodino Act. According to Biohaven, the transaction is also subject to other customary closing conditions that must be satisfied before the agreement becomes effective.