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Xenon Q1 Loss Narrower Than Expected, Pipeline Development in Focus
XENEXenon(XENE) ZACKS·2025-05-13 17:10

Core Viewpoint - Xenon Pharmaceuticals reported a narrower loss per share in Q1 2025 compared to estimates, while also generating modest revenue from collaborations, indicating ongoing development in its pipeline despite financial challenges [1][2]. Financial Performance - The company reported a loss of 83 cents per share for Q1 2025, which is an improvement from the loss of 94 cents estimated by Zacks and a loss of 62 cents in the same quarter last year [1]. - Revenues for the first quarter were 7.5million,slightlybelowtheZacksConsensusEstimateof7.5 million, slightly below the Zacks Consensus Estimate of 8 million, with no revenues reported in the year-ago quarter [2]. - Research and development (R&D) expenses increased by 38.1% year over year to 61.2million,primarilyduetocostsassociatedwithlatestageepilepsystudiesandtheinitiationofaphaseIIIstudyformajordepressivedisorder(MDD)[4].Generalandadministrativeexpensesroseto61.2 million, primarily due to costs associated with late-stage epilepsy studies and the initiation of a phase III study for major depressive disorder (MDD) [4]. - General and administrative expenses rose to 19 million, up 28.4% year over year, attributed to increased personnel-related costs [5]. - As of March 31, 2025, the company had cash, cash equivalents, and marketable securities totaling 691.1million,downfrom691.1 million, down from 754.4 million at the end of 2024, which is expected to fund ongoing clinical developments through 2027 [6]. Pipeline Developments - Xenon's lead candidate, azetukalner, is undergoing late-stage studies for focal onset seizures (FOS), with two phase III studies (X-TOLE2 and X-TOLE3) evaluating different doses [8]. - The first top-line data readout from the X-TOLE2 study is now anticipated in early 2026, delayed from the previously expected second half of 2025 [8]. - The company is also evaluating azetukalner for primary generalized tonic-clonic seizures in a phase III study and has initiated a phase III study for MDD following a successful phase II study [9]. - Plans for a late-stage bipolar depression program are set to begin by mid-2025, addressing significant unmet medical needs [10]. - The company is advancing multiple preclinical candidates targeting various indications, with plans to file an investigational new drug application for its Nav1.7 candidate, XEN1701, in Q3 2025 [11].