Somatoform Disorders

On track for August 15, 2025 FDA PDUFA goal date TNX-102 SL is a non-opioid analgesic; if approved, TNX-102 SL would become the first new drug for treating fibromyalgia in more than 15 years Commercial planning for TNX-102 SL underway for launch in the fourth quarter of 2025 March 24, 2025 -- Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (Tonix or the Company), a fully-integrated biopharmaceutical company with marketed products and a pipeline of development candidates, today announced that the U.S. Food and Drug Administration (FDA) will not require an Advisory Committee meeting to discuss the Company’s New Drug Application (NDA) for TNX-102 SL for the management of fibromyalgia. If approved, TNX-102 SL (cyclobenzaprine HCl sublingual tablets) would be the first new treatment option for fibromyalgia patients in 15 years. “We are pleased that FDA will not require an advisory committee meeting as part of the regulatory review process for TNX-102 SL,” said Seth Lederman, M.D., President, and Chief Executive Officer of Tonix Pharmaceuticals. “We believe that TNX-102 SL has the potential to be the first member of a new class of medicines for the management of fibromyalgia, a debilitating condition affecting over 10 million adults in the U.S. We believe we are well positioned to launch TNX-102 SL for the management of fibromyalgia in the fourth quarter of 2025 if approved by the FDA.” The FDA previously granted Fast Track designation to TNX-102 SL for the management of fibromyalgia in 2024, a designation intended to expedite FDA review of important new drugs to treat serious conditions and fill an unmet medical need. Fibromyalgia is a common chronic pain disorder that is understood to result from amplified sensory and pain signaling within the central nervous system, called central sensitization. Brain imaging studies have localized the functional disorder to the brain’s insula and anterior cingulate cortex. Fibromyalgia afflicts more than 10 million adults in the U.S., the majority of whom are women. Symptoms of fibromyalgia include chronic widespread pain, non-restorative sleep, fatigue, and brain fog (or cognitive dysfunction). Other associated symptoms include mood disturbances, including depression, anxiety, headaches and abdominal pain or cramps. Individuals suffering from fibromyalgia often struggle with their daily activities, have impaired quality of life, and frequently are disabled. Physicians and patients report common dissatisfaction with currently marketed products. Fibromyalgia is now recognized as the prototypic nociplastic syndrome and as a chronic overlapping pain condition (COPC) 1-3. Nociplastic pain is the third primary type of pain in addition to nociceptive pain and neuropathic pain. Many patients present with pain syndromes that are mixtures of the three primary types of pain. Nociplastic syndromes are associated with central and peripheral sensitization. Fibromyalgia can occur without any identifiable precipitating event. However, many fibromyalgia cases follow one or more precipitating event(s) including: post-operative pain, acute or chronic nociceptive or neuropathic pain states; recovery from an infectious illness; a cancer diagnosis or cancer treatment; a metabolic or endocrine stress; or a traumatic event. In the cases of recovery from an infectious illness, fibromyalgia is considered an Infection-Associated Chronic Condition. In addition to fibromyalgia cases associated with other conditions or stressors, the U.S. National Academies of Sciences, Engineering, and Medicine, has concluded that fibromyalgia is a diagnosable condition that can occur after recovery from COVID-19 in the context of Long COVID. Fibromyalgia is also recognized as a Chronic Overlapping Pain Condition, which is a group of related conditions that include chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME), irritable bowel syndrome, endometriosis, low back pain, post-concussive syndrome (also known as mild traumatic brain injury), chronic Lyme Disease, chronic diabetic neuropathy and chronic post-herpetic neuralgia. TNX-102 SL is a centrally acting, non-opioid investigational drug, designed for chronic use. The tablet is a patented sublingual formulation of cyclobenzaprine hydrochloride developed for bedtime dosing for the management of fibromyalgia. Cyclobenzaprine potently binds and acts as an antagonist at four different post-synaptic neuroreceptor subtypes: serotonergic-5-HT2A, adrenergic-α1, histaminergic-H1, and muscarinic-M1-cholinergic receptors. Together, these interactions are believed to target the non-restorative sleep characteristic of fibromyalgia identified by Professor Harvey Moldofsky in 1975. Cyclobenzaprine is not associated with risk of addiction or dependence. The TNX-102 SL tablet is based on a eutectic formulation of cyclobenzaprine HCl and mannitol that provides a stable product which dissolves rapidly and delivers cyclobenzaprine by the transmucosal route efficiently into the bloodstream. The eutectic protects cyclobenzaprine HCl from interacting with the basifying agent that is also part of the formulation and required for efficient transmucosal absorption. Patents based on TNX-102 SL’s eutectic composition and its properties have issued in the U.S., E.U., Japan, China and many other jurisdictions around the world and provide market protection into 2034. The European Patent Office’s Opposition Division maintained Tonix’s European Patent EP 2 968 992 in unamended form after an Opposition was filed against it by a Sandoz subsidiary, Hexal AG. Hexal AG did not appeal that decision. The formulation of TNX-102 SL was designed specifically for sublingual administration and transmucosal absorption for bedtime dosing to target disturbed sleep, while reducing the risk of daytime somnolence. Clinical pharmacokinetic studies indicated that relative to oral cyclobenzaprine, TNX-102 SL results in higher levels of exposure during the first 2 hours after dosing and in deceased levels of the long-lived active metabolite, norcyclobenzaprine in both single dose and multiple dose studies, consistent with bypassing first pass hepatic metabolism. At steady state after 20 days of dosing TNX-102 SL, the dynamic peak level of cyclobenzaprine is higher than the background level of norcyclobenzaprine. In contrast, after 20 days of dosing oral cyclobenzaprine, the simulated peak level of cyclobenzaprine is lower than the simulated background level of norcyclobenzaprine. 1Fitzcharles MA, et al. Lancet. 2021;397:2098-110 2Clauw DJ. Ann Rheum Dis. Published Online First: 2024 3Kaplan CM, et al. Nat Rev Neurol. 2024;20, 347–363 Tonix is a fully-integrated biopharmaceutical company focused on transforming therapies for pain management and vaccines for public health challenges. Tonix’s development portfolio is focused on central nervous system (CNS) disorders. Tonix’s priority is to advance TNX-102 SL, a product candidate for the management of fibromyalgia, for which an NDA was submitted based on two statistically significant Phase 3 studies for the management of fibromyalgia and for which a PDUFA (Prescription Drug User Fee act) goal date of August 15, 2025 has been assigned for a decision on marketing authorization. The FDA has also granted Fast Track designation to TNX-102 SL for the management of fibromyalgia. TNX-102 SL is also being developed to treat acute stress reaction and acute stress disorder under a Physician-Initiated IND at the University of North Carolina in the OASIS study funded by the U.S. Department of Defense (DoD). Tonix’s CNS portfolio includes TNX-1300 (cocaine esterase), a biologic in Phase 2 development designed to treat cocaine intoxication that has FDA Breakthrough Therapy designation, and its development is supported by a grant from the National Institute on Drug Abuse. Tonix’s immunology development portfolio consists of biologics to address organ transplant rejection, autoimmunity and cancer, including TNX-1500, which is an Fc-modified humanized monoclonal antibody targeting CD40-ligand (CD40L or CD154) being developed for the prevention of allograft rejection and for the treatment of autoimmune diseases. TNX-1500 has completed a positive Phase I trial. Tonix’s infectious disease portfolio includes TNX-801, a vaccine in development for mpox and smallpox, as well as TNX-4200 for which Tonix has a contract with the U.S. DoD’s Defense Threat Reduction Agency (DTRA) for up to $34 million over five years. TNX-4200 is a small molecule broad-spectrum antiviral agent targeting CD45 for the prevention or treatment of infections to improve the medical readiness of military personnel in biological threat environments. Tonix owns and operates a state-of-the art infectious disease research facility in Frederick, Md. Tonix Medicines, our commercial subsidiary, markets Zembrace® SymTouch® (sumatriptan injection) 3 mg and Tosymra® (sumatriptan nasal spray) 10 mg for the treatment of acute migraine with or without aura in adults. The content above comes from the network. if any infringement, please contact us to modify.

Top-line results from a three-week trial of Biohaven’s bipolar disorder candidate reveal no statistically significant difference between comparator and treatment.\n Biohaven’s bipolar disorder candidate has failed to improve mania symptoms in a phase 2/3 trial.The registrational study assessed BHV-7000, a drug designed to selectively activate Kv7.2/Kv7.3, an ion channel involved in neuronal signaling and regulation. An estimated 250 participants with bipolar I disorder were enrolled, with participants randomized to receive 75 mg of the investigational drug or comparator once a day.Top-line results from the three-week trial reveal no statistically significant difference between comparator and treatment, as measured by change in Young Mania Rating Scale total score, according to the company’s quarterly earnings release shared March 3. The scale consists of 11 items used to evaluate symptoms of mania.Specific data were not shared. Biohaven said it is conducting additional analyses and expects to present the full data set at an upcoming scientific meeting, according to the release.BHV-7000 was well tolerated, with no serious treatment-emergent adverse events reported. Most adverse events were mostly mild and resolved spontaneously, the company said.The investigational treatment has \"shown an impressive tolerability profile,\" William Blair analysts wrote in a March 4 note, citing the lack of CNS adverse events, such as dizziness, that are often tied to other antiseizure and psychiatric meds. Biohaven designed BHV-7000 using its Kv7 platform and is considering the candidate as a potential treatment for pain disorders, according to the company’s website.The asset is currently being evaluated in three other phase 2/3 studies across major depressive disorder (MDD), focal epilepsy and generalized epilepsy. The MDD findings are slated for release in the second half of this year, while focal epilepsy results are expected in the first half of next year.The upcoming MDD data will be \"key for determining the overall competitive profile of the drug in an evolving Kv7-potentiator space,\" the William Blair analysts wrote. In a separate release, also posted March 3, Biohaven detailed early-stage clinical findings for its subcutaneous small molecule asset dubbed BHV-1300. The ongoing phase 1 study found that 1000 mg of BHV-1300 per week reduced total IgG by up to 84% for patients with Graves’ disease.The reduction slightly exceeds those seen in subcutaneously administered FcRN-targeted therapies, such as 600 mg weekly of Immunovant\'s IMVT-1402, which showed a mean reduction of 74% with weekly dosing in a phase 1 trial of healthy adults.Biohaven\'s four-week study found the asset to be safe and well tolerated, according to the company. A phase 2 trial will be launched in the same indication in mid-2025, with additional follow-on studies in other autoimmune diseases also expected.The protein degrader is designed to selectively target IgG1, 2 and 4 while sparing IgG3.“Biohaven\'s unique extracellular degrader technology leverages the body\'s natural hepatic clearance mechanism to remove targeted antibodies contributing to disease and promises to usher in a new era of tunable, selective and self-administered immune therapy,” Chief Translational Officer Tova Gardin, M.D., said in the release.Biohaven’s stock dropped 14% Monday, sinking from $36.95 at market open to $32 by the end of the day.Editor\'s note: This story was updated at 9:30 a.m. ET on March 4 to include analysis from William Blair.

Presents progress and new anticipated milestones across portfolio of more than 10 assets and 6 therapeutic areas. Announces multiple advancements across the MoDETM (molecular degraders of extracellular proteins) platform and the next generation TRAPTM (targeted removal of aberrant protein) degraders, including: IgA Nephropathy (IgAN) program: First-in-human dosing with BHV-1400, a next generation TRAP degrader, achieved rapi­d, deep, and selective lowering of only aberrant galactose-deficient IgA1 (Gd-IgA1), the antibody causing IgA nephropathy, while sparing normal IgA. This selective and rapid approach to immunoglobulin lowering represents a second-generation therapeutic approach to IgAN, potentially allowing for strong disease control with less acute or long-term safety risks associated with complement inhibition or broad antibody suppression. The first and lowest dose tested (125mg) of BHV-1400 in the ongoing Phase 1 achieved rapid lowering of Gd-IgA1 with a median reduction of 60% within four hours of administration after a single dose. Maximal reduction exceeding 70% was observed within eight hours. Reductions were sustained for days even after a single dose. This rapid reduction of Gd-IgA1 is unprecedented in drugs targeting Gd-IgA1 and could allow for potential indications in situations where rapid Gd-IgA1 lowering could be beneficial in addition to chronic active disease and long-term maintenance. BHV-1400 has been safe and well-tolerated in the Phase 1 study to date and demonstrated no clinically significant changes in innate or adaptive immunity, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM. There were no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. No dose limiting toxicities have been observed in the Phase 1 to date and further dose escalation is planned to explore the full range of Gd-IgA1 reductions possible with BHV-1400. A pivotal trial in IgA nephropathy is planned using an accelerated regulatory path forward upon completion of the Phase 1 trial. Peripartum cardiomyopathy (PPCM) program: First-in-human dosing with BHV-1600, a TRAP degrader of β1AR autoantibodies, was initiated and has been well-tolerated to date after the first two dose cohorts without clinically relevant changes in innate or adaptive immunity, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM. There were no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. β1AR autoantibodies are thought to cause peripartum cardiomyopathy, a rare form of heart failure that develops at the end of pregnancy or in the months following delivery and in severe cases, can be life-threatening. BHV-1600 has been shown to bind to β1AR autoantibodies in preclinical studies and biomarker levels will be measured in women with PPCM later in development. Completed INTERACT meeting with FDA regarding BHV-1600 in 4Q 2024; gained alignment for the study design to potentially pursue an accelerated approval pathway in PPCM. IgG degrader programs: BHV-1300: Advanced optimized subcutaneous formulation with deep reductions of targeted IgG >60% demonstrated in the lowest dose cohort of the MAD, in line with modeling projections and with differentiated safety profile. There were no clinically significant reductions in IgG3, IgA, IgE, IgM, or albumin, no liver function test abnormalities, nor increases in cholesterol compared to baseline. Phase 1 completing last remaining dose cohorts with the optimized subcutaneous formulation in 1H 2025. Lead indication for BHV-1300 announced in Graves' Disease, a common autoimmune disorder affecting approximately 80 million people globally. Graves' Disease is caused by IgG1 autoantibodies that hyperstimulate the TSH receptor, causing hyperthyroidism can result in the need for surgical removal, chemical ablation of the thyroid, or need for chronic anti-thyroid drugs. Additional programs in rheumatoid arthritis and myasthenia gravis also continue to be pursued with BHV-1300 and 1310. Study May Proceed letter received from FDA for BHV-1310 IND, a novel IgG degrader and Phase 1 initiating in 1H 2025. BHV-1300 and BHV-1310 are similar but will optimize therapeutic targeting and facilitate broader commercial development options. Next generation degrader targets advancing in 2025 include: IgG4 specific degrader, PLA2R autoantibody degrader for membranous nephropathy, pro-insulin autoantibody degrader for type 1 diabetes, and TSH receptor autoantibody degrader as a selective follow-on asset for Graves' Disease. IgA Nephropathy (IgAN) program: First-in-human dosing with BHV-1400, a next generation TRAP degrader, achieved rapi­d, deep, and selective lowering of only aberrant galactose-deficient IgA1 (Gd-IgA1), the antibody causing IgA nephropathy, while sparing normal IgA. This selective and rapid approach to immunoglobulin lowering represents a second-generation therapeutic approach to IgAN, potentially allowing for strong disease control with less acute or long-term safety risks associated with complement inhibition or broad antibody suppression. The first and lowest dose tested (125mg) of BHV-1400 in the ongoing Phase 1 achieved rapid lowering of Gd-IgA1 with a median reduction of 60% within four hours of administration after a single dose. Maximal reduction exceeding 70% was observed within eight hours. Reductions were sustained for days even after a single dose. This rapid reduction of Gd-IgA1 is unprecedented in drugs targeting Gd-IgA1 and could allow for potential indications in situations where rapid Gd-IgA1 lowering could be beneficial in addition to chronic active disease and long-term maintenance. BHV-1400 has been safe and well-tolerated in the Phase 1 study to date and demonstrated no clinically significant changes in innate or adaptive immunity, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM. There were no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. No dose limiting toxicities have been observed in the Phase 1 to date and further dose escalation is planned to explore the full range of Gd-IgA1 reductions possible with BHV-1400. A pivotal trial in IgA nephropathy is planned using an accelerated regulatory path forward upon completion of the Phase 1 trial. Peripartum cardiomyopathy (PPCM) program: First-in-human dosing with BHV-1600, a TRAP degrader of β1AR autoantibodies, was initiated and has been well-tolerated to date after the first two dose cohorts without clinically relevant changes in innate or adaptive immunity, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM. There were no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. β1AR autoantibodies are thought to cause peripartum cardiomyopathy, a rare form of heart failure that develops at the end of pregnancy or in the months following delivery and in severe cases, can be life-threatening. BHV-1600 has been shown to bind to β1AR autoantibodies in preclinical studies and biomarker levels will be measured in women with PPCM later in development. Completed INTERACT meeting with FDA regarding BHV-1600 in 4Q 2024; gained alignment for the study design to potentially pursue an accelerated approval pathway in PPCM. IgG degrader programs: BHV-1300: Advanced optimized subcutaneous formulation with deep reductions of targeted IgG >60% demonstrated in the lowest dose cohort of the MAD, in line with modeling projections and with differentiated safety profile. There were no clinically significant reductions in IgG3, IgA, IgE, IgM, or albumin, no liver function test abnormalities, nor increases in cholesterol compared to baseline. Phase 1 completing last remaining dose cohorts with the optimized subcutaneous formulation in 1H 2025. Lead indication for BHV-1300 announced in Graves' Disease, a common autoimmune disorder affecting approximately 80 million people globally. Graves' Disease is caused by IgG1 autoantibodies that hyperstimulate the TSH receptor, causing hyperthyroidism can result in the need for surgical removal, chemical ablation of the thyroid, or need for chronic anti-thyroid drugs. Additional programs in rheumatoid arthritis and myasthenia gravis also continue to be pursued with BHV-1300 and 1310. Study May Proceed letter received from FDA for BHV-1310 IND, a novel IgG degrader and Phase 1 initiating in 1H 2025. BHV-1300 and BHV-1310 are similar but will optimize therapeutic targeting and facilitate broader commercial development options. Next generation degrader targets advancing in 2025 include: IgG4 specific degrader, PLA2R autoantibody degrader for membranous nephropathy, pro-insulin autoantibody degrader for type 1 diabetes, and TSH receptor autoantibody degrader as a selective follow-on asset for Graves' Disease. This selective and rapid approach to immunoglobulin lowering represents a second-generation therapeutic approach to IgAN, potentially allowing for strong disease control with less acute or long-term safety risks associated with complement inhibition or broad antibody suppression. The first and lowest dose tested (125mg) of BHV-1400 in the ongoing Phase 1 achieved rapid lowering of Gd-IgA1 with a median reduction of 60% within four hours of administration after a single dose. Maximal reduction exceeding 70% was observed within eight hours. Reductions were sustained for days even after a single dose. This rapid reduction of Gd-IgA1 is unprecedented in drugs targeting Gd-IgA1 and could allow for potential indications in situations where rapid Gd-IgA1 lowering could be beneficial in addition to chronic active disease and long-term maintenance. BHV-1400 has been safe and well-tolerated in the Phase 1 study to date and demonstrated no clinically significant changes in innate or adaptive immunity, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM. There were no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. No dose limiting toxicities have been observed in the Phase 1 to date and further dose escalation is planned to explore the full range of Gd-IgA1 reductions possible with BHV-1400. A pivotal trial in IgA nephropathy is planned using an accelerated regulatory path forward upon completion of the Phase 1 trial. Completed INTERACT meeting with FDA regarding BHV-1600 in 4Q 2024; gained alignment for the study design to potentially pursue an accelerated approval pathway in PPCM. BHV-1300: Advanced optimized subcutaneous formulation with deep reductions of targeted IgG >60% demonstrated in the lowest dose cohort of the MAD, in line with modeling projections and with differentiated safety profile. There were no clinically significant reductions in IgG3, IgA, IgE, IgM, or albumin, no liver function test abnormalities, nor increases in cholesterol compared to baseline. Phase 1 completing last remaining dose cohorts with the optimized subcutaneous formulation in 1H 2025. Lead indication for BHV-1300 announced in Graves' Disease, a common autoimmune disorder affecting approximately 80 million people globally. Graves' Disease is caused by IgG1 autoantibodies that hyperstimulate the TSH receptor, causing hyperthyroidism can result in the need for surgical removal, chemical ablation of the thyroid, or need for chronic anti-thyroid drugs. Additional programs in rheumatoid arthritis and myasthenia gravis also continue to be pursued with BHV-1300 and 1310. Study May Proceed letter received from FDA for BHV-1310 IND, a novel IgG degrader and Phase 1 initiating in 1H 2025. BHV-1300 and BHV-1310 are similar but will optimize therapeutic targeting and facilitate broader commercial development options. Progresses ion channel programs for bipolar, depression, epilepsy and pain: BHV-7000, a selective activator of Kv7.2/7.3 potassium channels: Continues to advance in clinical trials for bipolar disorder, depression, and epilepsy with multiple readouts over the next year, including expected topline for bipolar in 1H 2025 and depression in 2H 2025. BHV-2100, a TRPM3 ion channel antagonist: Preliminary data from an innovative laser-evoked hyperalgesia study with BHV-2100 reduced laser heat-induced pain and brain evoked potentials in healthy volunteers. These exciting results with BHV-2100 represent the first clinical proof of concept for the novel TRPM3 inhibitor class in pain, recapitulating powerful preclinical evidence of efficacy for this approach across a spectrum of pain disorders. BHV-7000, a selective activator of Kv7.2/7.3 potassium channels: Continues to advance in clinical trials for bipolar disorder, depression, and epilepsy with multiple readouts over the next year, including expected topline for bipolar in 1H 2025 and depression in 2H 2025. BHV-2100, a TRPM3 ion channel antagonist: Preliminary data from an innovative laser-evoked hyperalgesia study with BHV-2100 reduced laser heat-induced pain and brain evoked potentials in healthy volunteers. These exciting results with BHV-2100 represent the first clinical proof of concept for the novel TRPM3 inhibitor class in pain, recapitulating powerful preclinical evidence of efficacy for this approach across a spectrum of pain disorders. Highlights expansion of Biohaven's antibody drug conjugate (ADC) portfolio in Oncology, including: BHV-1510, a Trop2-directed ADC using a novel topoisomerase 1 (TopoIx) payload: Demonstration of early Phase 1 clinical activity, including tumor shrinkage, and safety with BHV-1510 in advanced or metastatic epithelial tumors. Based upon these results, Biohaven has entered into an expanded collaboration agreement with GeneQuantum providing exclusivity to the TopoIx payload for up to 18 ADC targets. BHV-1530, a FGFR3-directed ADC using the TopoIx payload: US IND clearance received for BHV-1530, potential indications include urothelial cancers and other solid tumors driven by FGFR3 alterations and/or upregulated FGFR3 protein expression. The first-in-human study is planned to commence in 1H 2025. Announced a multi-target collaboration with Merus, an oncology-focused biotechnology company developing innovative, multi-specific (Biclonics® and Triclonics®) antibodies, to co-develop three programs encompassing highly differentiated next generation dual-targeted bispecific ADCs leveraging Biohaven's proprietary conjugation and payload technologies and Merus' leading Biclonics technology platform. BHV-1510, a Trop2-directed ADC using a novel topoisomerase 1 (TopoIx) payload: Demonstration of early Phase 1 clinical activity, including tumor shrinkage, and safety with BHV-1510 in advanced or metastatic epithelial tumors. Based upon these results, Biohaven has entered into an expanded collaboration agreement with GeneQuantum providing exclusivity to the TopoIx payload for up to 18 ADC targets. BHV-1530, a FGFR3-directed ADC using the TopoIx payload: US IND clearance received for BHV-1530, potential indications include urothelial cancers and other solid tumors driven by FGFR3 alterations and/or upregulated FGFR3 protein expression. The first-in-human study is planned to commence in 1H 2025. Announced a multi-target collaboration with Merus, an oncology-focused biotechnology company developing innovative, multi-specific (Biclonics® and Triclonics®) antibodies, to co-develop three programs encompassing highly differentiated next generation dual-targeted bispecific ADCs leveraging Biohaven's proprietary conjugation and payload technologies and Merus' leading Biclonics technology platform. Based upon these results, Biohaven has entered into an expanded collaboration agreement with GeneQuantum providing exclusivity to the TopoIx payload for up to 18 ADC targets. Key late-stage programs advancing across important indications in 2025 also include: BHV-8000, a highly selective, brain-penetrant TYK2/JAK1 inhibitor that avoids class risks associated with JAK2/3 inhibition, expected to initiate pivotal trials in Parkinson's and Alzheimer's disease in 2025. Taldefgrobep alfa, a novel myostatin inhibitor optimized to block two key regulators of muscle and fat metabolism, continues to be developed in spinal muscular atrophy and obesity. New Drug Application (NDA) for troriluzole in all SCA genotypes was submitted to the FDA, following completion of pre-NDA meeting in 4Q 2024. Troriluzole has Orphan Drug and Fast-Track designations and qualifies for potential Priority Review. Awaiting filing decision from FDA and preparing for potential commercial launch in 2025 if approved. BHV-8000, a highly selective, brain-penetrant TYK2/JAK1 inhibitor that avoids class risks associated with JAK2/3 inhibition, expected to initiate pivotal trials in Parkinson's and Alzheimer's disease in 2025. Taldefgrobep alfa, a novel myostatin inhibitor optimized to block two key regulators of muscle and fat metabolism, continues to be developed in spinal muscular atrophy and obesity. New Drug Application (NDA) for troriluzole in all SCA genotypes was submitted to the FDA, following completion of pre-NDA meeting in 4Q 2024. Troriluzole has Orphan Drug and Fast-Track designations and qualifies for potential Priority Review. Awaiting filing decision from FDA and preparing for potential commercial launch in 2025 if approved. NEW HAVEN, Conn. , Jan. 13, 2025 /PRNewswire/ -- Biohaven Ltd. (NYSE: BHVN) (" Biohaven "), a global clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of innovative and transformative therapies to treat individuals with rare and common diseases, today highlighted broad portfolio progress at the 43rd Annual J.P. Morgan Healthcare Conference , including positive Phase 1 data for BHV-1400, its highly differentiated investigational therapeutic for IgA nephropathy. BHV-1400 is a second generation TRAP™ degrader from its proprietary MoDE™ platform. A copy of the slide presentation is available on the Events and Presentations section of the Biohaven website. Vlad Coric , M.D., Chairman and Chief Executive Officer of Biohaven , commented, "While we are excited about the significant progress across our entire portfolio, the first-ever data of a TRAP degrader in humans is monumental and unparalleled. The ability to only remove aberrant proteins causing disease while leaving all other immune functioning intact will usher in a new era of precision immunology. As quickly as science can identify new disease-causing proteins, our technology can quickly advance treatments for patients. I am proud of our dedicated, passionate and gifted team's unrelenting drive to transform medical care for patients suffering from severe diseases." Biohaven 2025 Portfolio Review and Anticipated Milestones Biohaven is positioned to achieve significant milestones in 2025 across a broad spectrum of early- and late-stage programs targeting indications with high unmet need: Molecular Degrader of Extracellular Proteins (MoDE) Platform: Biohaven's novel immune-modulating extracellular degrader platform harnesses selectivity, rapidity, and patient-friendly self-administration to remove disease-causing proteins from the body to potentially treat a wide range of diseases. Biohaven introduced next generation TRAP degraders, which are highly selective, each targeting a specific disease-causing protein for proteolysis. Four INDs for MoDE and next generation TRAP degrader molecules (targeting IgG1, IgG2, IgG4, Gd-IgA1, and β1AR autoantibodies) have been accepted by the FDA in 2024 with several additional investigational agents in development. Three assets have been dosed in Phase 1 trials with the fourth anticipated to be dosed in the first half of 2025. The first-of-its-kind molecule, BHV-1300 is being developed for the treatment of common immune-mediated diseases, such as Graves' Disease and Rheumatoid Arthritis. With patient-centered design, Biohaven has advanced a proprietary subcutaneous formulation of BHV-1300 and has entered into an agreement with Ypsomed, to develop and manufacture BHV-1300 in an easy-to-use, autoinjector for self-administration. This BHV-1300 proprietary formulation has demonstrated deep and targeted reductions of IgG, with reductions > 60% within four hours and 70% reduction within eight hours in the lowest subcutaneous dose tested in the MAD. Reductions were sustained even after just a single dose administration. Targeted IgG reductions (IgG1, IgG2, and IgG4, over IgG3) have been consistent with projected modeling. Phase 1 dose escalation is completing in 1H 2025, with Graves' Disease Phase 2 trial to initiate mid-year. BHV-1300 was rationally designed to spare IgG3 to preserve host immune defense. The selectivity of BHV-1300 demonstrated in the Phase 1 trial establishes a differentiated safety profile for the treatment of autoimmune disease relative to other IgG-lowering agents and validates the precision of the platform. BHV-1400 and BHV-1600, currently in Phase 1 clinical trials, represent the next generation TRAP degraders focused on selectively clearing very specific pathogenic antibodies, while sparing healthy immunoglobulin to preserve immune function. TRAP molecules commence a new age of immune-modulating treatments, targeted removal of disease-causing proteins for removal while sparing the normal function of the healthy immune system. Data from the first, and lowest, dose cohort of BHV-1400 demonstrated clear differentiation from competitors in the IgA nephropathy space, with rapid lowering of Gd-IgA1 within four hours and preservation of host immunoglobulins including IgG, IgA, IgE, and IgM. IgA nephropathy is a rare chronic kidney disease affecting young and middle-aged adults that is caused by Gd-IgA1 and leads to kidney failure in up to 40% of patients within 10-20 years. Taken in total, the selectivity of MoDE and TRAP degraders demonstrated to date refine immune-modulating treatment representing a clear next generation of drug development technology in immunoglobulin and extracellular protein lowering. Existing mechanisms, both pharmaceutical and device (plasmapheresis), broadly reduce immunoglobulins subclasses and/or isotypes, leading to inefficient dosing, safety risks, necessity of procedures, delays in therapy, and potential efficacy impacts. MoDE and TRAP's new paradigm builds off the prior successes of immune modulation, while also providing a novel technology to fine tune therapies for immune-mediated diseases. As described below, the implications and applications of this selective targeting could be multi-organ, multi-disease. IgA Nephropathy (IgAN) Program: First-in-human dosing with BHV-1400 achieved rapid, deep, and selective lowering of only Gd-IgA1, the aberrant antibody that causes IgA nephropathy, while sparing normal IgA. The first and lowest dose tested (125 mg) of BHV-1400 in Phase 1 achieved rapid lowering of Gd-IgA1 with a median reduction of 60% within four hours of administration. Maximal reduction exceeding 70% was observed within eight hours. Even after just a single dose administration of BHV-1400, reductions in Gd-IgA1 were sustained for days. The rapid reduction of Gd-IgA1 by BHV-1400 is unprecedented in drugs targeting Gd-IgA1 and could allow for potential indications in situations where rapid Gd-IgA1 lowering could be beneficial in addition to chronic active disease and long-term maintenance. The selective and rapid approach to Gd-IgA1 lowering of BHV-1400 represents a second-generation therapeutic approach to IgAN, potentially allowing for effective disease control with less acute- or long-term safety risks associated with B-cell directed therapy, complement inhibitors, or broad immunosuppression. BHV-1400 has been safe and well-tolerated in the Phase 1 study to date and demonstrated no clinically significant changes in innate or adaptive immune systems, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM, and no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. There have been no dose limiting toxicities observed in the Phase 1 study and dose escalation continues to explore the full range of Gd-IgA1 reductions possible with BHV-1400. A pivotal trial in IgA nephropathy is planned using an accelerated regulatory path upon completion of the Phase 1 trial. Additional opportunities in situations when rapid Gd-IgA1 reduction could be beneficial may also be feasible given the demonstrated dosing kinetics in the Phase 1 study. Biohaven further expands its renal franchise with the degrader platform, developing several investigational TRAPs for the treatment of immune-mediated renal disease, including a TRAP degrader to target PLA2R autoantibodies for the treatment of membranous nephropathy among others. The first and lowest dose tested (125 mg) of BHV-1400 in Phase 1 achieved rapid lowering of Gd-IgA1 with a median reduction of 60% within four hours of administration. Maximal reduction exceeding 70% was observed within eight hours. Even after just a single dose administration of BHV-1400, reductions in Gd-IgA1 were sustained for days. The rapid reduction of Gd-IgA1 by BHV-1400 is unprecedented in drugs targeting Gd-IgA1 and could allow for potential indications in situations where rapid Gd-IgA1 lowering could be beneficial in addition to chronic active disease and long-term maintenance. The selective and rapid approach to Gd-IgA1 lowering of BHV-1400 represents a second-generation therapeutic approach to IgAN, potentially allowing for effective disease control with less acute- or long-term safety risks associated with B-cell directed therapy, complement inhibitors, or broad immunosuppression. BHV-1400 has been safe and well-tolerated in the Phase 1 study to date and demonstrated no clinically significant changes in innate or adaptive immune systems, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM, and no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. There have been no dose limiting toxicities observed in the Phase 1 study and dose escalation continues to explore the full range of Gd-IgA1 reductions possible with BHV-1400. A pivotal trial in IgA nephropathy is planned using an accelerated regulatory path upon completion of the Phase 1 trial. Additional opportunities in situations when rapid Gd-IgA1 reduction could be beneficial may also be feasible given the demonstrated dosing kinetics in the Phase 1 study. Biohaven further expands its renal franchise with the degrader platform, developing several investigational TRAPs for the treatment of immune-mediated renal disease, including a TRAP degrader to target PLA2R autoantibodies for the treatment of membranous nephropathy among others. Peripartum cardiomyopathy (PPCM) program: First-in-human dosing with BHV-1600 has been safe and well-tolerated to date after two dose cohorts without clinically relevant changes in innate or adaptive immune systems, including white blood cells and immunoglobulins IgG, IgA, IgE, and IgM, and no clinically significant reductions in albumin, liver function test abnormalities, or increases in cholesterol compared to baseline. β1AR autoantibodies are thought to cause peripartum cardiomyopathy, a rare form of heart failure with no approved therapy that occurs at the end of pregnancy or following delivery and in severe cases, can be life-threatening. BHV-1600 has been shown to bind to β1AR autoantibodies in preclinical studies and biomarker levels will be measured in women with PPCM later in development. Completed INTERACT meeting with FDA regarding BHV-1600 in 4Q 2024 and gained alignment for the study design to potentially pursue an accelerated approval pathway in PPCM, a rare autoimmune life-threatening disease with no approved therapy. Completed INTERACT meeting with FDA regarding BHV-1600 in 4Q 2024 and gained alignment for the study design to potentially pursue an accelerated approval pathway in PPCM, a rare autoimmune life-threatening disease with no approved therapy. IgG MoDE degrader program: BHV-1300 Phase 1 is completing the last remaining dose cohorts with expected completion in 1H 2025. Study May Proceed letter received from the FDA for the BHV-1310 IND and Phase 1 initiating in 1H 2025. Lead indication for BHV-1300 announced in Graves' Disease, a common autoimmune disorder affecting approximately 3 million in the US and 80 million globally. Graves' Disease is caused by IgG1 autoantibodies that hyperstimulate the TSH receptor, causing hyperthyroidism and can result in the need for surgical removal, chemical ablation of the thyroid, or need for chronic anti-thyroid drug therapy. Additional programs in rheumatoid arthritis and myasthenia gravis also to be pursued with BHV-1300 and 1310. Study May Proceed letter received from FDA for BHV-1310 IND, a next generation IgG degrader and Phase 1 initiating in 1H 2025. BHV-1300 and BHV-1310 are similar but will optimize therapeutic targeting and facilitate broader commercial development options. Lead indication for BHV-1300 announced in Graves' Disease, a common autoimmune disorder affecting approximately 3 million in the US and 80 million globally. Graves' Disease is caused by IgG1 autoantibodies that hyperstimulate the TSH receptor, causing hyperthyroidism and can result in the need for surgical removal, chemical ablation of the thyroid, or need for chronic anti-thyroid drug therapy. Additional programs in rheumatoid arthritis and myasthenia gravis also to be pursued with BHV-1300 and 1310. Study May Proceed letter received from FDA for BHV-1310 IND, a next generation IgG degrader and Phase 1 initiating in 1H 2025. BHV-1300 and BHV-1310 are similar but will optimize therapeutic targeting and facilitate broader commercial development options. Next generation MoDE degrader targets advancing in 2025 include: IgG4 specific degrader PLA2R autoantibody degrader for membranous nephropathy Pro-insulin autoantibody degrader for type 1 diabetes TSH receptor autoantibody degrader as a selective follow-on asset for Graves' Disease IgG4 specific degrader PLA2R autoantibody degrader for membranous nephropathy Pro-insulin autoantibody degrader for type 1 diabetes TSH receptor autoantibody degrader as a selective follow-on asset for Graves' Disease Upcoming milestones in the degrader program include: IgG MoDE Degraders (1300/1310): BHV-1300 Phase 1 completing last remaining dose cohorts with the optimized subcutaneous formulation with expected completion in 1H 2025. BHV-1310 first-in-human study anticipated to initiate 1H 2025. Phase 2 study in Graves' Disease expected to initiate mid-2025 and additional programs in rheumatoid arthritis and myasthenia gravis continue to be pursued with BHV-1300/1310. Phase 1 with BHV-1400 and BHV-1600 expected to be completed in 1H 2025. Four molecules moving towards development candidate in 2025 including: IgG4 degrader, PLA2R autoantibody degrader, insulin autoantibody degrader, and TSH receptor autoantibody degrader. Tova Gardin , M.D., M.P.P, Biohaven Chief Translational Officer, reflected on the recent results from the MoDE degrader platform, "With the advancements across our degrader platform, including the highly selective TRAP molecules, Biohaven inaugurates a new age of immune-modulating treatment – one which opens the potential of treating the pathogenesis of disease with precision to restore healthy homeostasis. The results of BHV-1400 from the first and lowest SAD cohort highlight the speed, precision, and patient-centered innovation that drives development of each of our molecules. Lowering Gd-IgA1 by 60% within hours of dose administration, BHV-1400 realizes the precision possible with MoDE degraders: The possibility of selectively degrading the pathogenic driver of disease, leaving host immunity unperturbed. Innovation extends across the MoDE platform, with new programs launched for the treatment of Graves' Disease, peripartum cardiomyopathy, and other selective TRAP degraders advancing towards development candidate nominations to potentially treat membranous nephropathy, IgG4-mediated disease, and diabetes." BHV-2100: First-in-clinic, oral, selective TRPM3 antagonist that offers a novel, non-addictive treatment for migraine and neuropathic pain. Based on favorable pharmacokinetic and safety data from the Phase 1 studies in healthy subjects, a Phase 1b laser-evoked hyperalgesia trial was performed and a proof-of-concept in the acute treatment of migraine is ongoing. Preliminary data from the laser-evoked hyperalgesia study demonstrated that BHV-2100 reduced laser heat-induced pain and brain evoked potentials in healthy volunteers. This exciting result is a culmination of years of laboratory research and represents a powerful entree into the field. It provides the first indication of potential clinical efficacy in pain with the novel TRPM3 mechanism recapitulating antinociceptive preclinical efficacy across a spectrum of pain models. Data from the laser-evoked potential study and proof-of-concept migraine study expected in 1H 2025. BHV-7000: Selective activator of Kv7.2/7.3 potassium channels, a breakthrough target in neurology and neuropsychiatry with blockbuster potential. Kv7 activation is a clinically validated target for treating mood disorders and epilepsy. Registrational studies ongoing in bipolar disorder, major depressive disorder, focal epilepsy, and generalized epilepsy. Upcoming milestones in the BHV-7000 program include: Pivotal bipolar and major depressive disorder topline results expected in 1H 2025 and 2H 2025, respectively. Focal epilepsy study topline results expected in 1H 2026. Troriluzole: Troriluzole is a novel glutamate modulator currently in Phase 3 development for Spinocerebellar ataxia (SCA) and obsessive-compulsive disorder (OCD). A new drug application (NDA) was submitted to US FDA for troriluzole in all SCA genotypes, following completion of pre-NDA meeting in 4Q 2024. Troriluzole has Orphan Drug and Fast-Track designations and qualifies for potential Priority Review. EU marketing authorization application also under review for troriluzole in all SCA genotypes. There are no FDA-approved treatments for SCA. Additionally, two Phase 3 trials with troriluzole in OCD are ongoing. Upcoming milestones in the troriluzole program include: Preparing for commercial launch in SCA in 2025, while awaiting filing decision from FDA on the troriluzole all-genotype SCA NDA resubmission. Topline data from two Phase 3 OCD trials in 1H 2025 and 2H 2025, respectively. Taldefgrobep alfa: Taldefgrobep is a novel myostatin inhibitor that is optimized to block both myostatin and activin A signaling, two key regulators of muscle and fat metabolism. Biohaven is studying taldefgrobep in a global Phase 3 expansion study in Spinal Muscular Atrophy (SMA), as an adjunctive therapy to enhance muscle mass and function in patients treated with standard-of-care therapies. Analyses of prespecified subgroups by race and ethnicity demonstrated that the largest study population (87% Caucasian; n=180) showed clinically meaningful improvements on the MFM-32 at all timepoints, including Week 48, compared to the corresponding placebo+SOC group (p < 0.05), though the overall primary endpoint was not met. Robust target engagement (myostatin reduction) and beneficial impacts on body composition parameters (fat mass, lean muscle mass, and bone density) were noted, offering a potential paradigm shift in the treatment of obesity with opportunity to improve quality of weight loss; lower total body weight by specifically reducing fat mass while also preserving or increasing lean muscle mass. Upcoming milestones in the taldefgrobep program include: Expected FDA meeting to discuss SMA registrational path in 1H 2025. Initiate taldefgrobep Phase 2 study in obesity in 1H 2025. BHV-8000: BHV-8000 is a highly selective, oral, brain-penetrant, selective TYK2/JAK1 inhibitor with broad potential for neurodegenerative and neuroinflammatory disorders. In the Phase 1 SAD/MAD study in healthy participants, BHV-8000 was generally safe and well-tolerated while producing significant reductions in inflammatory biomarkers relative to placebo. Target indications for BHV-8000 include Parkinson's disease, Alzheimer's disease, prevention of amyloid-related imaging abnormalities (ARIA), and multiple sclerosis (MS). In 2024, Biohaven completed interactions with FDA enabling registrational programs for Parkinson's disease and the prevention of ARIA. Upcoming milestones in the BHV-8000 program include: Initiate BHV-8000 Phase 2/3 study in Parkinson's disease in 1H 2025 Advance Alzheimer's, MS and ARIA programs in 2025. Oncology antibody drug conjugate (ADC) portfolio: BHV-1510 (Trop2 ADC): Preliminary data from the initial Phase 1 study dosing cohorts of BHV-1510 have demonstrated promising clinical activity, including tumor shrinkage, with a tolerable safety profile of the novel topoisomerase 1 (TopoIx) payload. The Phase 1/2 study of BHV-1510 is progressing with robust enrollment in dose escalation and optimization, both as monotherapy and in combination with the anti-PD1 monoclonal antibody Libtayo® (cemiplimab-rwlc) through a clinical supply agreement with Regeneron. Preclinically, TopoIx has shown increased immunogenic cell death and synergistic activity when combined with anti-PD1/L1 checkpoint inhibitors, and a differentiated nonclinical toxicity profile; Clinical activity has been seen across dose cohorts tested to date, including the lowest dose tested of 2mg/kg Q3W; Early PK data demonstrates a stable ADC with very low serum concentrations of free payload; Preliminary safety data demonstrates a favorable profile, with no payload-associated interstitial lung disease, gastrointestinal toxicities, or significant hematological toxicities observed in early cohorts. The main toxicity observed thus far in Phase 1 study has been stomatitis, an expected on-target Trop2 class toxicity that has been manageable; Combination cohorts of BHV-1510 with Libtayo® have initiated. Based on these encouraging early results, Biohaven has entered into an expanded collaboration agreement with GeneQuantum, which provides broad target exclusivity for up to 18 ADC targets incorporating the novel topoisomerase 1 inhibitor (TopoIx) payload. Biohaven has incorporated the TopoIx payload into its next clinical-stage investigational agent, BHV-1530. BHV-1530 is an FGFR3-directed ADC with potential indications in cancers driven by FGFR3 alterations and/or upregulated FGFR3 protein expression, including urothelial cancers and other solid tumors. While FGFR3 has been clinically validated as a target in oncology, there are no other FGFR3 ADCs currently in clinical development. Biohaven retains global rights for BHV-1530 under the agreement via an exclusive license with GeneQuantum and Aimed Bio. The US IND has been opened, and a first-in-human study for solid tumors is planned for 1H 2025. In addition, Biohaven today announced a multi-target collaboration with Merus, an oncology-focused biotechnology company developing innovative, multi-specific (Biclonics® and Triclonics®) antibodies. This collaboration will co-develop three programs encompassing highly differentiated next generation dual-targeted bispecific ADCs leveraging Biohaven's proprietary conjugation and payload technologies along with Merus' leading Biclonics technology platform. Together, the announced milestones and collaborations represent a significant expansion of Biohaven's ADC portfolio, positioning the Company with potential to deliver highly differentiated therapeutics and address significant unmet needs in Oncology. Nushmia Khokhar , M.D., Biohaven Chief Medical Officer of Oncology, commented, "These are exciting times for Biohaven's oncology pipeline as we are well-positioned to introduce differentiated, next generation ADCs to the clinic. The early Phase 1 data with BHV-1510 is promising, showing not only signs of clinical activity but also minimal toxicities related to the free payload. This affirms the advantages of our conjugation technology, which provides high ADC stability. The distinct profile of the novel TopoIx payload, and its potential to synergize with checkpoint inhibitor therapy, could significantly benefit patients across various cancer types. Furthermore, our collaboration with Merus and the expanded partnership with GeneQuantum—utilizing the TopoIx payload for multiple targets—demonstrate the potential of Biohaven's upcoming innovative ADCs. This includes dual-targeting ADCs, which are exciting for their potential to address challenges like tumor heterogeneity and delivery of stable ADCs with an improved therapeutic index." Upcoming milestones in the oncology program include: Interim Phase 1 data with BHV-1510 and dose optimization as monotherapy and combination therapy with Libtayo® in epithelial tumors in 2025. Initiate Phase 1 trial of BHV-1530 in 1H 2025. Advance Merus collaboration ADCs (undisclosed targets) and TopoIx ADCs in 2025. About Biohaven Biohaven is a biopharmaceutical company focused on the discovery, development, and commercialization of life-changing treatments in key therapeutic areas, including immunology, neuroscience, and oncology. Biohaven is advancing its innovative portfolio of therapeutics, leveraging its proven drug development experience and multiple proprietary drug development platforms. Biohaven's extensive clinical and nonclinical programs include Kv7 ion channel modulation for epilepsy and mood disorders; extracellular protein degradation for immunological diseases; TRPM3 antagonism for migraine and neuropathic pain; TYK2/JAK1 inhibition for neuroinflammatory disorders; glutamate modulation for OCD and SCA (spinocerebellar ataxia); myostatin inhibition for neuromuscular and metabolic diseases, including SMA and obesity; antibody recruiting bispecific molecules and antibody drug conjugates for cancer. For more information, visit www.biohaven.com. Forward-looking StatementsThis news release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The use of certain words, including "continue", "plan", "will", "believe", "may", "expect", "anticipate" and similar expressions, is intended to identify forward-looking statements. Investors are cautioned that any forward-looking statements, including statements regarding the future development, timing and potential marketing approval and commercialization of development candidates, are not guarantees of future performance or results 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 US regulatory requirements; the potential commercialization of Biohaven's product candidates; and the effectiveness and safety of Biohaven's product candidates. Additional important factors to be considered in connection with forward-looking statements are described in Biohaven's filings with the Securities and Exchange Commission , including within the sections titled "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 any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law. MoDE is a trademark of Biohaven Therapeutics Ltd.TRAP is a trademark of Biohaven Therapeutics Ltd. Biclonics and Triclonics are registered trademarks of Merus NV.Libtayo® is a registered trademark of Regeneron. Investor Contact: Jennifer Porcelli Vice President, Investor Relationsjennifer.porcelli@biohavenpharma.com+1 (201) 248-0741 Media Contact: Mike Beyer Sam Brown Inc. mikebeyer@sambrown.com+1 (312) 961-2502 View original content to download multimedia:https://www.prnewswire.com/news-releases/biohaven-highlights-portfolio-progress-innovation-and-anticipated-milestones-at-the-43rd-annual-jp-morgan-healthcare-conference-reports-positive-degrader-data-with-rapid-deep-and-selective-lowering-of-galactose-deficient-ig-302349336.html SOURCE Biohaven Ltd.