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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/07/09/3324800/0/en/teva-and-polpharma-biologics-announce-global-licensing-agreement-for-a-biosimilar-candidate-to-ocrevus-ocrelizumab-for-multiple-sclerosis.html">Teva und Polpharma Biologics kündigen globale Lizenzvereinbarung für einen Biosimilar‑Kandidaten zu Ocrevus® (ocrelizumab) gegen Multiple Sklerose an</a>
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        Teva sichert sich exklusive weltweite Rechte zur Vermarktung des Biosimilar‑Kandidaten von Polpharma Biologics zu Ocrevus® (ocrelizumab), einschließlich sowohl intravenöser als auch subkutaner Formulierungen. Die Vereinbarung stärkt Tevas Pivot to Growth‑Strategie, indem sie die Biosimilars‑Pipeline durch strategische Kooperationen erweitert.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/18/3314541/0/en/Teva-Submits-NDA-for-Ecopipam-a-First-in-Class-Investigational-Therapy-for-Pediatric-Tourette-Syndrome.html">Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</a>
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        TEL AVIV, Israel, June 18, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a first-in-class investigational therapy for the treatment of pediatric Tourette syndrome.
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        <div class="me-2 text-gray">vor 4 Monaten</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260611949436/en/Paragon-Advances-Registration-Ready-CNS-Asset-Addressing-Important-Unmet-Need-and-Closes-Sale-to-Teva-Pharmaceutical/">Paragon Advances Registration-Ready CNS Asset Addressing Important Unmet Need and Closes Sale to Teva Pharmaceutical</a>
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        CHICAGO--(BUSINESS WIRE)--Paragon Biosciences today announced the closing of the sale of Emalex Biosciences to Teva Pharmaceutical, reinforcing Paragon&#39;s ability to build innovative biotechnology companies that deliver important treatments to the patients who need them. Emalex is another Paragon Biosciences-founded company built to develop a novel class of treatment for patients with central ne...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/10/3309960/0/en/Teva-Closes-Acquisition-of-Emalex-Biosciences-Strengthening-Late-Stage-Neuroscience-Pipeline-and-Advancing-Pivot-to-Growth-Strategy.html">Teva Closes Acquisition of Emalex Biosciences, Strengthening Late-Stage Neuroscience Pipeline and Advancing Pivot to Growth Strategy</a>
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        TEL AVIV, Israel, June 10, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA), today announced the closing of Teva&#39;s acquisition of Emalex Biosciences, strengthening its late-stage pipeline with ecopipam and further advancing its Pivot to Growth strategy. Phase 3 data for ecopipam were recently published in JAMA Neurology , and a U.S. NDA submission is anticipate...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/08/3308026/0/en/Teva-s-Data-on-AUSTEDO-deutetrabenazine-tablets-and-AUSTEDO-XR-deutetrabenazine-extended-release-tablets-Highlight-Long-Term-Advances-in-Tardive-Dyskinesia-Treatment-and-Care.html">Teva&#39;s Data on AUSTEDO® (deutetrabenazine) tablets and AUSTEDO XR® (deutetrabenazine) extended-release tablets Highlight Long-Term Advances in Tardive Dyskinesia Treatment and Care</a>
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        PARSIPPANY, N.J. and TEL AVIV, Israel, June 08, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA), today announced new data that highlight the comprehensive tardive dyskinesia (TD) symptom improvement from treatment with AUSTEDO® and AUSTEDO XR®. The new findings, drawn from three separate studies, were presented at Psyc...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/05/3307494/0/en/Teva-Presents-New-Data-on-AUSTEDO-deutetrabenazine-tablets-and-AUSTEDO-XR-deutetrabenazine-extended-release-tablets-that-Show-Patient-and-Caregiver-Reported-Improvements-in-Hunting.html">Teva Presents New Data on AUSTEDO® (deutetrabenazine) tablets and AUSTEDO XR® (deutetrabenazine) extended-release tablets that Show Patient- and Caregiver-Reported Improvements in Huntington&#39;s Disease Chorea</a>
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        PARSIPPANY, N.J. and TEL AVIV, Israel, June 05, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA), today announced new data from the first and only real-world, decentralized study evaluating the patient- and caregiver-reported quality of life impacts of Huntington&#39;s disease (HD) chorea3 and the effect of AUSTEDO® or AUST...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/01/3304731/0/en/Teva-to-Present-at-the-Goldman-Sachs-Global-Healthcare-Conference.html">Teva to Present at the Goldman Sachs Global Healthcare Conference</a>
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        PARSIPPANY, N.J., and TEL AVIV, Israel, June 01, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced that Richard Francis, Teva&#39;s President and CEO, will participate in a fireside chat at the Goldman Sachs Global Healthcare Conference on Monday, June 8, 2026. The fireside chat will begin at 8:00 A.M. Eastern Time.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/21/3299597/0/en/The-European-Medicines-Agency-Accepts-Teva-s-Marketing-Authorization-Application-for-Olanzapine-Long-Acting-Injectable-TEV-749-for-the-Treatment-of-Schizophrenia-in-Adults.html">The European Medicines Agency Accepts Teva&#39;s Marketing Authorization Application for Olanzapine Long-Acting Injectable (TEV-‘749) for the Treatment of Schizophrenia in Adults</a>
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        TEL AVIV, Israel and PARIS, May 21, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceuticals International GmbH, a subsidiary of Teva Pharmaceutical Industries Ltd. (NYSE: and TASE: TEVA) and Medincell (Euronext: MEDCL), today announced that the European Medicines Agency (EMA) has accepted the Marketing Authorization Application (MAA) for olanzapine long-acting injectable (TEV-‘749) for the treatment of s...
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