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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Biomarin-Pharmaceutical-US09061G1013">Biomarin Pharmaceutical</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/biomarin-reports-second-quarter-2026-financial-and-operating-results-302845167.html">BioMarin veröffentlicht Finanz- und Betriebsergebnisse für das zweite Quartal 2026</a>
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        Gesamtumsatz im zweiten Quartal 2026 stieg im Jahresvergleich um 20 % auf 990 Mio. USD Stärkeres Wachstumserwartungen führen zu erhöhter Prognose für den Gesamtumsatz 2026, VOXZOGO® und Non-GAAP verwässertes Ergebnis je Aktie (EPS) Die Ergänzung durch GALAFOLD® und POMBILITI® + OPFOLDA®, mit Kostensynergien, wird voraussichtlich das Umsatzwachstum beschleunigen, Non-GAAP verwässertes EPS erhöhe...
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/biomarin-and-n-lorem-foundation-enter-early-research-collaboration-to-develop-potential-first-in-disease-medicine-for-newly-identified-renu-syndrome-302835235.html">BioMarin und n-Lorem Foundation schließen frühe Forschungspartnerschaft zur Entwicklung eines potenziellen First‑in‑Disease-Medikaments für neu identifiziertes ReNU-Syndrom</a>
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        ReNU-Syndrom wurde 2024 entdeckt und es gibt keine zugelassenen Medikamente für die Erkrankung Die Zusammenarbeit kombiniert BioMarins Führungsrolle in genetischen Arzneimitteln mit n-Lorems wegweisender Antisense-Expertise Ein experimentelles Antisense-Oligonukleotid (ASO) zielt darauf ab, die zugrundeliegende genetische Ursache dieser schweren neuroentwicklungsbedingten Erkrankung anzugehen S...
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/us-food-and-drug-administration-accepts-biomarins-supplemental-new-drug-application-for-full-approval-of-voxzogo-vosoritide-for-children-with-achondroplasia-302823072.html">U.S. Food and Drug Administration nimmt BioMarins ergänzende Zulassungsanmeldung für die Vollzulassung von VOXZOGO® (vosoritide) bei Kindern mit Achondroplasie an</a>
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        Die Anmeldung basiert auf Langzeitdaten zur Sicherheit und Wirksamkeit aus drei laufenden Studien, einschließlich Erwachsenenhöhe und zusätzlichen klinischen Endpunkten über das lineare Längenwachstum hinaus, darunter Körperproportionalität und Armlänge, bewertet über langfristige Nachbeobachtung. FDA-PDUFA-Zieldatum für die Entscheidung: 28. Feb. 2027. SAN RAFAEL, Calif., 13. Juli 2026 /PRNews...
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/biomarin-announces-new-three-year-voxzogo-vosoritide-data-in-hypochondroplasia-and-bmn-333-early-results-at-endo-2026-302800847.html">BioMarin Announces New Three-Year VOXZOGO® (vosoritide) Data in Hypochondroplasia and BMN 333 Early Results at ENDO 2026</a>
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        Data from an investigator-led study showed treatment with VOXZOGO resulted in sustained improvements in growth over three years in children with hypochondroplasia New Phase 1 results also presented for investigational BMN 333 support potential weekly dosing in children with achondroplasia SAN RAFAEL, Calif., June 16, 2026 /PRNewswire/ -- BioMarin Pharmaceutical Inc. (Nasdaq: BMRN) announced new...
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/biomarins-drug-shows-significant-growth-gains-children-late-stage-trial-2026-05-20/">BioMarin&#39;s drug shows significant growth gains in children in late-stage trial</a>
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        BioMarin Pharmaceutical said on Wednesday its treatment for a rare condition that leads to ​short stature helped boost growth in ‌children, meeting the main goal of a late-stage study and sending shares up nearly 5% in extended ​trading.
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/biomarin-announces-positive-phase-3-pivotal-study-results-for-voxzogo-vosoritide-in-children-with-hypochondroplasia-302778176.html">BioMarin Announces Positive Phase 3 Pivotal Study Results for VOXZOGO® (vosoritide) in Children with Hypochondroplasia</a>
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        Study met primary endpoint, exceeding expectations with a highly statistically significant improvement in annualized growth velocity (AGV, change from baseline) of 2.33 cm/yr compared to placebo at week 52, as well as statistically significant increases in standing height and height Z-score Study demonstrated statistically significant improvement in arm span at week 52 compared to placebo, a ke...
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/biomarins-genetic-disease-therapy-shows-mixed-results-late-stage-study-2026-05-18/">BioMarin&#39;s genetic disease therapy shows mixed results in late-stage study</a>
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        BioMarin Pharmaceutical said on Monday its ​experimental treatment for a ‌rare genetic condition met one of the two main goals ​in a late-stage study.
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/biomarin-provides-update-on-phase-3-trial-for-bmn-401-in-children-aged-1-12-with-enpp1-deficiency-302774207.html">BioMarin Provides Update on Phase 3 Trial for BMN 401 in Children Aged 1-12 With ENPP1 Deficiency</a>
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        ENERGY 3 study met 1 of 2 co-primary endpoints in children with ENPP1 deficiency Treatment with BMN 401 led to statistically significant increases in plasma inorganic pyrophosphate (PPi) concentration, one of the study&#39;s co-primary endpoints; however, no improvement was observed in Radiographic Global Impression of Change (RGI-C) scores, the study&#39;s other co-primary endpoint and an important cl...
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