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Patients can engage in gamified versions of objective behavioural activities on a tablet. Credit: © 2025 Department of Psychiatry, Warneford Hospital, Oxford, OX3 7JX. Boehringer Ingelheim, the University of Oxford and Cumulus Neuroscience have launched a study to monitor brain activity in individuals with borderline personality disorder (BPD) using new technology. The study will offer insights into the daily experiences of individuals with psychiatric disorders. It aims to assess the acceptability of new technology designed to quantify the mood, behaviour and activity of the brain, and aid new therapeutic research and development. The NeuLogiq neuroassessment platform from Cumulus will be leveraged in the BPD patient population for the first time. It allows for brain function tracking over time, both in clinical settings and in patients’ homes. The NeuLogiq headset enables individuals to engage in gamified versions of objective behavioural activities on a tablet. GlobalData Strategic Intelligence US Tariffs are shifting - will you react or anticipate? Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis. By GlobalData Learn more about Strategic Intelligence The headset measures electroencephalogram (EEG) brain wave patterns that are accurately synchronised with the activities. The goal is to capture data that offers a clearer understanding of the activity within the brain’s networks. The Department of Psychiatry at the University of Oxford will carry out the study at Warneford Hospital, gathering frequent EEG and behavioural evaluations and remote metrics of mood and activity. The study targets young adults aged 18 to 35 years and aims to evaluate the Cumulus platform’s feasibility in this population to offer a dataset for in-depth analysis of brain activity and behaviour in BPD. 30 BPD subjects and 20 subjects who have not been diagnosed with mental health disorders will be recruited. Boehringer Ingelheim neuroscience and mental health global head and senior vice-president Dr Hugh Marston stated: “If this platform is successfully validated in this patient population, it could be a game-changer for studies investigating novel precision psychiatry treatments. It could help us identify biomarkers for stratification and provide a rich dataset for reverse translation.” Boehringer recently entered a strategic research partnership with Cue Biopharma to develop and commercialise Cue’s CUE-501 product candidate for autoimmune conditions.

Ingelheim, Germany, Oxford and Belfast, UK, April 29, 2025 – Boehringer Ingelheim, the University of Oxford, and Cumulus Neuroscience are joining forces to provide insights into the day-to-day experiences of people living with psychiatric disorders, and how these experiences relate to their brain activity. The first-of-its-kind study will use novel technology to quantify brain activity, mood, and behavior at home in people who have been diagnosed with borderline personality disorder (BPD), an often neglected group of patients. The aims are to explore the acceptability of this technology in patients and gain quantitative, fine-grained, insights that could potentially guide the research and development of much-needed new therapies. Current clinical and lab-based assessments rely on retrospective recall of symptoms. They are thus limited by how accurately patients remember past events and only provide a snapshot in time of an individual’s clinical state. Moreover, self-reported questionnaires lack objectivity. This can lead to an incomplete or inaccurate picture of the overall experience of the individual and the failure of new medicines in clinical studies. This new study aims to change that. It will use Cumulus´ NeuLogiq® neuroassessment platform for the first time in people diagnosed with borderline personality disorder. This platform enables the tracking of brain function over time, both in the clinic, and from the comfort of a study participant’s home. Participants use a tablet to perform gamified versions of established objective behavioral tasks, while wearing the NeuLogiq headset which records EEG (electroencephalogram) brain waves that are precisely time-synced to the tasks. The intent is to capture data that will provide a more accurate picture of brain network activity.  In 2019, one in eight people worldwide were estimated to be living with a mental health condition, and half of the adult population can expect to experience a mental illness by age 75.i,ii*  People diagnosed with severe mental health conditions experience reduced life expectancy relative to the general population, with around 14 years of potential life lost,1 and the economic consequences of mental health conditions can be enormous.iii That’s why Boehringer Ingelheim is embracing ‘Precision Psychiatry’. This in-depth research approach delves into the neurobiology of symptoms with the goal of uncovering more targeted and holistic treatment solutions that address specific symptoms in people living serious mental illness to help them to live fulfilling lives. Kate Saunders, Associate Professor in the Department of Psychiatry of the University of Oxford says, “People diagnosed with borderline personality disorder experience a range of symptoms, including changeable mood, impulsivity, and associated difficulties in interpersonal relationships, all of which can have a significant impact on their lives. We're looking forward to exploring this new technology in people living with BPD, in collaboration with the scientists at Cumulus and Boehringer Ingelheim, to gain new insights into the mechanisms which underpin the symptoms people given this diagnosis experience.  This could open up pathways for the development of new therapies.” Dr. Hugh Marston, Senior Vice President and Global Head Neuroscience & Mental Health, Boehringer Ingelheim says, “Boehringer Ingelheim is committed to developing novel therapeutics to address the major unmet needs of people living with mental health disorders. If this platform is successfully validated in this patient population, it could be a game-changer for studies investigating novel precision psychiatry treatments. It could help us identify biomarkers for stratification and provide a rich dataset for reverse-translation.” “Many psychiatric conditions disrupt cognitive function, meaning that patients may find it harder to manage their daily life or continue to work effectively,” said Brian Murphy, PhD, Co-founder and Chief Scientific Officer of Cumulus. “These underappreciated symptoms can change from day to day, so frequent real-world measurement is important if we want to find new therapies that improve activities of daily living and quality of life. Today, we are fortunate that wearable technologies and AI are enabling a new era of drug development where we can understand objectively how a drug affects cognitive function and the underlying brain mechanisms that drive it.”  The study will be conducted by the Department of Psychiatry of the University of Oxford at the Warneford Hospital. It will frequently collect EEG and behavioral assessments, alongside remote measures of mood and activity. The main aims are to assess the feasibility of using the Cumulus platform in young adults aged 18-35 and to provide a rich dataset about brain activity and behavior in BPD for in-depth analysis.  Thirty participants who have been diagnosed with BPD and 20 participants with no diagnosed mental health disorder will be recruited. Dr. Lauren Atkinson, from the Department of Psychiatry who will be senior researcher on the study says, “We are looking forward to working with people diagnosed with borderline personality disorder and prioritising research important to them. One of the key features of a BPD diagnosis is affective dysregulation. By regularly capturing mood, alongside measures of brain activity and cognitive function over an extended period of time, we hope to better capture patient experience and use objective measures to understand more about what is happening at those key moments.” *The mental health conditions studied in this epidemiological research included: panic disorder and/or agoraphobia, generalized anxiety disorder, post-traumatic stress disorder, social phobia, specific phobia, major depressive disorder, bipolar disorder, alcohol abuse disorder, alcohol dependence disorder, drug abuse disorder, drug dependence disorder, attention deficit/hyperactivity disorder, and intermittent explosive disorder.About Boehringer Ingelheim Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry’s top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,500 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at www.boehringer-ingelheim.com (global) or www.boehringer-ingelheim.com/uk (UK). About Cumulus Neuroscience Our mission is to generate the data and insights required to accelerate the diagnosis and management of central nervous system (CNS) disorders for millions of patients and caregivers around the world. At Cumulus Neuroscience we are advancing NeuLogiq®, an AI-based, multi-domain digital biomarker platform designed with 10 of the world's leading pharma companies. This novel platform provides the critical data and insights needed for faster, more robust and cost-effective decision-making in clinical trials and patient care. NeuLogiq enables study sponsors to capture large amounts of real-world clinical data repeatedly over time, across multiple behavioral and physiological domains, in the clinic and at home. Together with machine learning (ML) analytics, Cumulus simplifies and improves the robustness of CNS clinical trials, providing objective assessment of study inclusion and treatment outcomes. About Oxford University The University Department of Psychiatry’s mission is to conduct world-class research, teach psychiatry to medical students, develop future researchers in a graduate programme, teach doctors in training, promote excellence in clinical practice, and develop and provide innovative clinical services. It supports research in four key areas: neurobiology, psychological treatments, developmental psychiatry and social psychiatry. The Department is committed to the translation of scientific discovery into benefits for patients. www.psych.ox.ac.uk  Oxford University has been placed number 1 in the Times Higher Education World University Rankings for the ninth year running, and ​number 3 in the QS World Rankings 2024. At the heart of this success are the twin-pillars of our ground-breaking research and innovation and our distinctive educational offer. Oxford is world-famous for research and teaching excellence and home to some of the most talented people from across the globe. Our work helps the lives of millions, solving real-world problems through a huge network of partnerships and collaborations. The breadth and interdisciplinary nature of our research alongside our personalised approach to teaching sparks imaginative and inventive insights and solutions. Through its research commercialisation arm, Oxford University Innovation, Oxford is the highest university patent filer in the UK and is ranked first in the UK for university spinouts, having created more than 300 new companies since 1988. Over a third of these companies have been created in the past five years. The university is a catalyst for prosperity in Oxfordshire and the United Kingdom, contributing £15.7 billion to the UK economy in 2018/19, and supports more than 28,000 full time jobs. Media Contacts  Boehringer Ingelheim: Dr. Reinhard Malin Boehringer Ingelheim Corporate Center GmbH  Innovation Unit/Bio Comms, Corp. Affairs  Media + PR  press@boehringer-ingelheim.com  Cumulus:Tina Sampath tina.sampath@cumulusneuro.com Oxford University: Lisa Jones Communications Manager Department of Psychiatry, University of Oxford, Warneford Hospital lisa.jones@psych.ox.ac.uk 

Issued 12,765,958 new sharesPriced at €2.35 per share, representing a 15.44% discount on the 5-day VWAPStrong investor demand, with the offering significantly oversubscribed€15 million anchored by a leading US institutional investorProceeds to fund clinical development and corporate initiatives MADRID and CAMBRIDGE, Mass., April 24, 2025 (GLOBE NEWSWIRE) -- Oryzon Genomics, S.A. (ISIN Code: ES0167733015, ORY), a clinical-stage biopharmaceutical company and a European leader in epigenetics, announced today the successful completion of a €30 million capital increase through the issuance of 12,765,958 new shares, priced at €2.35 per share. This pricing reflects a 15.44% discount to the 5-day volume-weighted average price (VWAP) of €2.779 per share prior to April 22, 2025, and a 19.38% discount to the April 22 closing price of €2.915. The offering, which was structured as straight equity with no warrants attached, attracted strong demand and was significantly oversubscribed. A US-based institutional investor anchored the round with a €15 million order, with the remaining demand filled by investors across the US, Europe, and Spain. The capital increase was capped at €30 million by the company’s Board of Directors. Maxim (U.S.), All-Invest (EU/UK), and Singular Bank (Spain) acted as bookrunners. Banco Sabadell, S.A. acted as the Settlement and Technical Pre-financing Agent for the Capital Increase, while Gómez-Acebo & Pombo Abogados, S.L.P. (Spanish law) and Gibson, Dunn & Crutcher LLP (U.S. law) served as legal advisors to the Company, and Loeb & Loeb LLP acted as U.S. legal counsel to Maxim Group LLC. The funds raised will be used to: Advance the clinical development of vafidemstat for the treatment of aggression in CNS disorders such as Borderline Personality Disorder (BPD) and Autism Spectrum Disorder (ASD)Expand ongoing clinical programs in oncology and hematologySupport CMC activities and preparations for Phase IIb-III trials, as well as other regulatory initiativesStrengthen the company's balance sheet to support future partnership or M&A negotiationsCover general administrative expenses and financial obligationsEnhance legal and audit readiness for a potential dual listing on Nasdaq Dr. Carlos Buesa, CEO of Oryzon, commented: “This financing marks a key milestone that enables us to continue progressing our clinical programs with vafidemstat in aggression-related CNS disorders and to further develop our oncology and hematology pipeline. It also reinforces our financial position, supporting strategic conversations with investors and potential partners.” About OryzonFounded in 2000 in Barcelona, Spain, Oryzon (ISIN Code: ES0167733015) is a clinical stage biopharmaceutical company and the European leader in epigenetics, with a strong focus on personalized medicine in CNS disorders and oncology. Oryzon’s team is composed of highly qualified professionals from the pharma industry located in Barcelona, Boston, and San Diego. Oryzon has an advanced clinical portfolio with two LSD1 inhibitors, vafidemstat in CNS (Phase III-ready) and iadademstat in oncology (Phase II). The company has other pipeline assets directed against other epigenetic targets like HDAC-6 where a clinical candidate ORY-4001, has been nominated for its possible development in CMT and ALS. In addition, Oryzon has a strong platform for biomarker identification and target validation for a variety of malignant and neurological diseases. For more information, visit www.oryzon.com About IadademstatIadademstat (ORY-1001) is a small oral molecule, which acts as a highly selective inhibitor of the epigenetic enzyme LSD1 and has a powerful differentiating effect in hematologic cancers (see Maes et al., Cancer Cell 2018 Mar 12; 33 (3): 495-511.e12.doi: 10.1016 / j.ccell.2018.02.002.). A FiM Phase I/IIa clinical trial with iadademstat in R/R AML patients demonstrated the safety and good tolerability of the drug and preliminary signs of antileukemic activity, including a CRi (see Salamero et al, J Clin Oncol, 2020, 38(36): 4260-4273. doi: 10.1200/JCO.19.03250). Iadademstat has shown encouraging safety and strong clinical activity in combination with azacitidine in a Phase IIa trial in elder 1L AML patients (ALICE trial) (see Salamero et al., ASH 2022 oral presentation & The Lancet Haematology, 2024, 11(7):e487-e498). Iadademstat is currently being evaluated in combination with gilteritinib in the ongoing Phase Ib FRIDA trial in patients with relapsed/refractory AML with FLT3 mutations, and in combination with azacitidine and venetoclax in 1L AML in an investigator-initiated study led by OHSU and in a trial sponsored by the U.S. National Cancer Institute (NCI) under the Cooperative Research and Development Agreement (CRADA) signed between Oryzon and the NCI to collaborate on further clinical development of iadademstat in different types of hematologic and solid cancers. Beyond hematological cancers, the inhibition of LSD1 has been proposed as a valid therapeutic approach in some solid tumors such as small cell lung cancer (SCLC), neuroendocrine tumors (NET), medulloblastoma and others. In a Phase IIa trial in combination with platinum/etoposide in second line ED-SCLC patients (CLEPSIDRA trial), preliminary activity and safety results have been reported (see Navarro et al., ESMO 2018 poster). Iadademstat is in a collaborative Phase II trial with the Fox Chase Cancer Center (FCCC) in combination with paclitaxel in R/R neuroendocrine carcinomas, and in a Phase I/II randomized trial in 1L ED-SCLC in combination with ICI sponsored by NCI and led by the Memorial Sloan Kettering Cancer Center. Oryzon is further expanding the clinical development of iadademstat through additional investigator-initiated studies. Iadademstat has orphan drug designation for SCLC in the US and for AML in the US and EU. About Vafidemstat Vafidemstat (ORY-2001) is an oral, CNS-optimized LSD1 inhibitor. The molecule acts on several levels: it reduces cognitive impairment, including memory loss and neuroinflammation, and at the same time has neuroprotective effects. In animal studies vafidemstat not only restores memory but reduces the exacerbated aggressiveness of SAMP8 mice, a model for accelerated aging and Alzheimer’s disease (AD), to normal levels and also reduces social avoidance and enhances sociability in murine models. In addition, vafidemstat exhibits fast, strong, and durable efficacy in several preclinical models of multiple sclerosis (MS). Oryzon has performed two Phase IIa clinical trials in aggressiveness in patients with different psychiatric disorders (REIMAGINE, see Ferrer et al, Psychiatry & Clin Neurosci, 2025, doi.org/10.1111/pcn.13800) and in aggressive/agitated patients with moderate or severe AD (REIMAGINE-AD), with positive clinical results reported in both. Additional finalized Phase IIa clinical trials with vafidemstat include the ETHERAL trial in patients with Mild to Moderate AD, where a significant reduction of the inflammatory biomarker YKL40 was observed after 6 and 12 months of treatment, and the pilot, small-scale SATEEN trial in Relapse-Remitting and Secondary Progressive MS, where anti-inflammatory activity was also observed. Vafidemstat has also been tested in a Phase II in severe Covid-19 patients (ESCAPE) assessing the capability of the drug to prevent ARDS, one of the most severe complications of the viral infection, where it showed significant anti-inflammatory effects in severe Covid-19 patients. Vafidemstat is currently advancing as a Phase III-ready asset in Borderline Personality disorder (BPD) following completion of the global, randomized, double blind Phase IIb PORTICO trial (final data presented at ECNP-2024). Following receipt of the minutes from the End-of-Phase II meeting with the FDA to discuss PORTICO’s results, the company announced plans to move forward with a Phase III PORTICO-2 trial in agitation/aggression in BPD (FDA submission planned in 1H2025). Vafidemstat is also being investigated in a double-blind, randomized, placebo-controlled Phase IIb trial in negative symptoms of schizophrenia (EVOLUTION trial, recruitment ongoing). The company is also deploying a CNS precision medicine approach with vafidemstat in genetically-defined patient subpopulations of certain CNS disorders and is evaluating a clinical trial in Kabuki Syndrome patients. The company is also exploring the clinical development of vafidemstat in other neurodevelopmental syndromes. FORWARD-LOOKING STATEMENTS This communication contains, or may contain, forward-looking information and statements about Oryzon, including financial projections and estimates and their underlying assumptions, statements regarding plans, objectives, and expectations with respect to future operations, capital expenditures, synergies, products and services, and statements regarding future performance. Forward-looking statements are statements that are not historical facts and are generally identified by the words “expects,” “anticipates,” “believes,” “intends,” “estimates” and similar expressions. Although Oryzon believes that the expectations reflected in such forward-looking statements are reasonable, investors and holders of Oryzon shares are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Oryzon that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include those discussed or identified in the documents sent by Oryzon to the Spanish Comisión Nacional del Mercado de Valores (CNMV), which are accessible to the public. Forward-looking statements are not guarantees of future performance and have not been reviewed by the auditors of Oryzon. You are cautioned not to place undue reliance on the forward-looking statements, which speak only as of the date they were made. All subsequent oral or written forward-looking statements attributable to Oryzon or any of its members, directors, officers, employees, or any persons acting on its behalf are expressly qualified in their entirety by the cautionary statement above. All forward-looking statements included herein are based on information available to Oryzon on the date hereof. Except as required by applicable law, Oryzon does not undertake any obligation to publicly update or revise any forward‐looking statements, whether as a result of new information, future events, or otherwise. This document does not constitute an offer or invitation to purchase or subscribe shares in accordance with the provisions of Regulation (EU) 2017/1129 of the European Parliament and of the Council of 14 June 2017, and/or the restated text of the Securities Market Law, approved by Law 6/2023 of 17 March, and its implementing regulations. Nothing in this document constitutes investment advice. In addition, this document does not constitute an offer of purchase, sale or exchange, nor a request for an offer of purchase, sale or exchange of securities, nor a request for any vote or approval in any jurisdiction. The shares of Oryzon Genomics, S.A. may not be offered or sold in the United States of America except pursuant to an effective registration statement under the Securities Act of 1933 or pursuant to a valid exemption from registration.. Spain Oryzon IR & Media, Europe & US Patricia Cobo/Mario Cordera Emili Torrell Sandya von der Weid Atrevia Chief BD Officer LifeSci Advisors, LLC +34 91 564 07 25 +34 673 33 97 65 +34 93 515 1313 +41 78 680 05 38 pcobo@atrevia.com mcordera@atrevia.com etorrell@oryzon.com svonderweid@lifesciadvisors.com