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Equity Research Biohaven Ltd. : Key Takeaways from AES 2024 & Mgmt Catch Up December 11, 2024 Biohaven Ltd. : Key Takeaways from AES 2024 & Mgmt Catch Up * Analysts * Print * PDF Biohaven Ltd. : Key Takeaways from AES 2024 & Mgmt Catch Up This document is being provided for the exclusive use of erickrueger@synovus.com. 11 December 2024 BIOHAVEN LTD. KEY TAKEAWAYS FROM AES 2024 & MGMT CATCH UP J.P. Morgan does and seeks to do business with companies covered in its research reports. As a result, investors should be aware that the firm may have a conflict of interest that could affect the objectivity of this report. Investors should consider this report as only a single factor in making their investment decision. Read full disclosures Overweight BHVN, BHVN US Price (10 Dec 24):$42.59 The authors wish to thank Adhiraj S Chauhan, of the J.P. Morgan Global Research Center, for contributions to this report. Over the weekend, we attended the AES Annual Meeting (Dec. 6-10, 2024; Los Angeles, CA) and we wanted to provide our key takeaways from the expanded phase 1 MAD safety results for BHV-7000 including the once-daily extended-release (ER) formulation which were presented in a poster as well as our brief catch up with mgmt (CMO, Irfan Qureshi) wherein we covered a number of topics relevant to the rest of the pipeline. At a high level, the ER formulation of BHV-7000 was safe and well-tolerated in healthy adults which we find important given the extended-release tablets are currently being evaluated in doses up to 75mg once daily in the ongoing phase 2 and 3 studies in focal epilepsy, idiopathic generalized epilepsy, bipolar mania, and major depressive disorder (MDD). In our catch up, mgmt expressed that they are very happy with the phase 1 profile of BHV-7000 and its clean safety and tolerability thus far including the low rates of CNS-related TEAEs and in particular the results with the ER formulation; moreover, they emphasized the potential opportunities for the asset in bipolar disorder and MDD. We agree with mgmt that these findings support the continued clinical development of BHV-7000 with the potential to reduce seizures while minimizing AEs; we have similarly heard from doctors in the past and at the conference that there remains a continued need for efficacious anti-seizure medications (ASMs) with minimal burden around AEs. Net-net, we continue to strongly recommend BHVN for investors looking for growth harboring a diverse set of opportunities and to the extent that some of them are derisked could drive the stock further as we round out 2024 and head into 2025 (see our latest view/further details in our biotech outlook here). * Details on the expanded phase 1 MAD safety results for BHV-7000, including the ER formulation.The update included data on the healthy adults who were randomized to receive the ER formulation of BHV-7000 (25mg, 50mg, or 75mg once daily) or placebo for up to 15 days (Poster 1.486). Of note, there were only 2 nervous system TEAEs reported in one patient each that were mild in severity with one being presyncope at the 25mg ER dose and the other being dysgeusia at the 50mg ER dose; in our catch up, mgmt was unconcerned by these events and stressed that they were mild and self-resolving. Of note, there were no severe or serious AEs and no cases of cognitive/mood disturbances or somnolence reported. Overall, this study demonstrated favorable safety and tolerability of BHV-7000 with no dose-limiting AEs. We have heard in our conversations that at the same time the doctors are eager to better understand how the drug performs with respect to seizure reduction in patients in this context. We are hosting a call with Dr. Kathryn Davis (University of Pennsylvania) on Dec. 12 at 2pm ET to discuss BHV-7000 clinical results and prospects as well as the epilepsy competitive landscape in more detail (please contact the team for details). * Other pipeline tidbits. Regarding the recent results from the phase 3 RESILIENT study for taldefgrobep alfa (t-alfa) in spinal muscular atrophy (SMA) which did not meet its primary endpoint (see our prior comments here), mgmt continues to look at the data and plans to engage with the FDA on a potential path forward. Despite the primary endpoint miss in RESILIENT, mgmt indicated they were really excited by the dual energy x-ray absorptiometry (DXA)/body composition data (i.e., fat mass, lean muscle mass and bone density) from the study in particular; recall, Biohaven cited the demonstrated target engagement (i.e., myostatin reduction) and taldefgrobep-associated changes in body composition as support for the decision to advance t-alfa into a placebo-controlled phase 2 obesity study in 4Q24. Further, they reaffirmed to us their plan to provide an update on BHV-1300 (see our prior comments here and deep dive here) and submit a total of 4 INDs from the MoDE platform in 2024 as well as re-submit the NDA for troriluzole in spincerebellar ataxia (SCA) in 4Q24. We think the positive topline BHV4157-206-RWE results set troriluzole for a potential broad label encompassing all SCA genotypes in the U.S. and a strong launch around mid-2025, if/when approved. In the EU, EMA marketing authorization remains under review. Show Disclosures Companies Discussed in This Report (all prices in this report as of market close on 10 December 2024, unless otherwise indicated)Biohaven Ltd.(BHVN/$42.59/OW) Analyst Certification: The Research Analyst(s) denoted by an “AC” on the cover of this report certifies (or, where multiple Research Analysts are primarily responsible for this report, the Research Analyst denoted by an “AC” on the cover or within the document individually certifies, with respect to each security or issuer that the Research Analyst covers in this research) that: (1) all of the views expressed in this report accurately reflect the Research Analyst’s personal views about any and all of the subject securities or issuers; and (2) no part of any of the Research Analyst's compensation was, is, or will be directly or indirectly related to the specific recommendations or views expressed by the Research Analyst(s) in this report. For all Korea-based Research Analysts listed on the front cover, if applicable, they also certify, as per KOFIA requirements, that the Research Analyst’s analysis was made in good faith and that the views reflect the Research Analyst’s own opinion, without undue influence or intervention. All authors named within this report are Research Analysts who produce independent research unless otherwise specified. In Europe, Sector Specialists (Sales and Trading) may be shown on this report as contacts but are not authors of the report or part of the Research Department. Important Disclosures * Market Maker/ Liquidity Provider: J.P. Morgan is a market maker and/or liquidity provider in the financial instruments of/related to Biohaven Ltd.. * Manager or Co-manager: J.P. Morgan acted as manager or co-manager in a public offering of securities or financial instruments (as such term is defined in Directive 2014/65/EU) of/for Biohaven Ltd. within the past 12 months. * Client: J.P. Morgan currently has, or had within the past 12 months, the following entity(ies) as clients: Biohaven Ltd.. * Client/Investment Banking: J.P. Morgan currently has, or had within the past 12 months, the following entity(ies) as investment banking clients: Biohaven Ltd.. * Client/Non-Investment Banking, Securities-Related: J.P. Morgan currently has, or had within the past 12 months, the following entity(ies) as clients, and the services provided were non-investment-banking, securities-related: Biohaven Ltd.. * Investment Banking Compensation Received: J.P. Morgan has received in the past 12 months compensation for investment banking services from Biohaven Ltd.. * Potential Investment Banking Compensation: J.P. Morgan expects to receive, or intends to seek, compensation for investment banking services in the next three months from Biohaven Ltd.. * Non-Investment Banking Compensation Received: J.P. Morgan has received compensation in the past 12 months for products or services other than investment banking from Biohaven Ltd.. * Debt Position: J.P. Morgan may hold a position in the debt securities of Biohaven Ltd., if any. Company-Specific Disclosures: Important disclosures, including price charts and credit opinion history tables, are available for compendium reports and all J.P. Morgan–covered companies, and certain non-covered companies, by visiting https://www.jpmm.com/research/disclosures, calling 1-800-477-0406, or e-mailing research.disclosure.inquiries@jpmorgan.com with your request. Date Rating Price ($) Price Target ($) 04-Jan-23 OW 13.50 23 25-Apr-23 OW 13.87 20 17-May-23 OW 13.87 21 15-Jun-23 OW 24.38 27 16-Aug-23 OW 20.75 24 06-Sep-23 OW 17.77 26 20-Nov-23 OW 30.09 32 23-Feb-24 OW 47.33 56 07-Mar-24 OW 58.13 57 19-May-24 OW 37.37 55 03-Oct-24 OW 47.99 68 The chart(s) show J.P. Morgan's continuing coverage of the stocks; the current analysts may or may not have covered it over the entire period. J.P. Morgan ratings or designations: OW = Overweight, N= Neutral, UW = Underweight, NR = Not Rated Explanation of Equity Research Ratings, Designations and Analyst(s) Coverage Universe: J.P. Morgan uses the following rating system: Overweight (over the duration of the price target indicated in this report, we expect this stock will outperform the average total return of the stocks in the Research Analyst’s, or the Research Analyst’s team’s, coverage universe); Neutral (over the duration of the price target indicated in this report, we expect this stock will perform in line with the average total return of the stocks in the Research Analyst’s, or the Research Analyst’s team’s, coverage universe); and Underweight (over the duration of the price target indicated in this report, we expect this stock will underperform the average total return of the stocks in the Research Analyst’s, or the Research Analyst’s team’s, coverage universe. NR is Not Rated. In this case, J.P. Morgan has removed the rating and, if applicable, the price target, for this stock because of either a lack of a sufficient fundamental basis or for legal, regulatory or policy reasons. The previous rating and, if applicable, the price target, no longer should be relied upon. An NR designation is not a recommendation or a rating. In our Asia (ex-Australia and ex-India) and U.K. small- and mid-cap Equity Research, each stock’s expected total return is compared to the expected total return of a benchmark country market index, not to those Research Analysts’ coverage universe. If it does not appear in the Important Disclosures section of this report, the certifying Research Analyst’s coverage universe can be found on J.P. Morgan’s Research website, https://www.jpmorganmarkets.com. Coverage Universe: Romero, Tessa T : ACADIA Pharmaceuticals (ACAD), Agios Pharmaceuticals (AGIO), Biohaven Ltd. (BHVN), Cytokinetics (CYTK), Dyne Therapeutics (DYN), Edgewise Therapeutics (EWTX), EyePoint Pharmaceuticals (EYPT), Generation Bio (GBIO), Lexeo Therapeutics (LXEO), Neumora Therapeutics (NMRA), Sana Biotechnology (SANA), Scholar Rock (SRRK), Seres Therapeutics (MCRB), Upstream Bio (UPB), Xenon Pharmaceuticals (XENE) J.P. Morgan Equity Research Ratings Distribution, as of October 05, 2024 Overweight(buy) Neutral(hold) Underweight(sell) J.P. Morgan Global Equity Research Coverage* 49% 38% 13% IB clients** 50% 46% 38% JPMS Equity Research Coverage* 46% 41% 13% IB clients** 71% 67% 54% *Please note that the percentages may not add to 100% because of rounding.**Percentage of subject companies within each of the "buy," "hold" and "sell" categories for which J.P. Morgan has provided investment banking services within the previous 12 months. 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