<turbo-stream action="append" target="news"><template>  <div class="row mb-4 py-2 news-box">
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Roche-CH1499059983">Roche</a></div>
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        <div class="me-2 text-gray">22 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20261015174934/en/FDA-Approves-Genentech%E2%80%99s-Enspryng-a-First-in-Class-IL-6R-Inhibitor-as-the-First-and-Only-At-Home-Subcutaneous-Treatment-Option-for-Thyroid-Eye-Disease-TED/">FDA Approves Genentech&#39;s Enspryng, a First-in-Class IL-6R Inhibitor, as the First and Only At-Home Subcutaneous Treatment Option for Thyroid Eye Disease (TED)</a>
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        SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)---- $RHHBY--Genentech, a member of the Roche Group (SIX: RO, ROP; OTCQX: RHHBY), announced today that the U.S. Food and Drug Administration (FDA) has approved Enspryng® (satralizumab-mwge) for the treatment of adults with thyroid eye disease (TED), providing patients with the first and only at-home subcutaneous treatment option. Enspryng can be admin...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Roche-CH1499059983">Roche</a></div>
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        <div class="me-2 text-gray">22 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/10/16/3382249/0/en/fda-approves-roche-s-enspryng-a-first-in-class-il-6r-inhibitor-as-the-first-and-only-at-home-subcutaneous-treatment-option-for-thyroid-eye-disease-ted.html">FDA approves Roche&#39;s Enspryng, a first-in-class IL-6R inhibitor, as the first and only at-home subcutaneous treatment option for thyroid eye disease (TED)</a>
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        Basel, 16 October 2026 - Roche (SIX: RO, ROP; OTCQX: RHHBY) announced today that the U.S. Food and Drug Administration (FDA) has approved Enspryng® (satralizumab) for the treatment of adults with thyroid eye disease (TED), providing patients with the first and only at-home subcutaneous treatment option. Enspryng can be administered by a person living with TED or a caregiver following training f...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Roche-CH1499059983">Roche</a></div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">25 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/roche-strikes-obesity-drug-licensing-deal-worth-up-116-bln-with-chinese-rona-2026-10-13/">Roche strikes obesity drug licensing deal worth up to $1.16 bln with Chinese Rona Therapeutics</a>
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        Roche strikes obesity drug licensing deal worth up to $1.16 bln with Chinese Rona Therapeutics
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Roche-CH1499059983">Roche</a></div>
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        <div class="me-2 text-gray">28 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20261010064674/en/Genentech-Presents-New-Phase-III-One-Year-Data-for-Vamikibart-in-Uveitic-Macular-Edema-UME-a-Serious-Cause-of-Vision-Loss/">Genentech Presents New Phase III One-Year Data for Vamikibart in Uveitic Macular Edema (UME), a Serious Cause of Vision Loss</a>
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        SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)---- $RHHBY--Genentech, a member of the Roche Group (SIX: RO, ROP; OTCQX: RHHBY), announced today new one-year data from the Phase III MEERKAT and SANDCAT studies evaluating investigational vamikibart compared with a sham procedure that mimics intravitreal (IVT) injections in adults with uveitic macular edema (UME). Across both studies, data continue ...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Roche-CH1499059983">Roche</a></div>
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        <div class="me-2 text-gray">29 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20261009492482/en/FDA-Approves-Genentech%E2%80%99s-Tecentriq-in-Combination-With-a-Fluoropyrimidine-and-Oxaliplatin-for-the-Adjuvant-Treatment-of-a-Certain-Type-of-Stage-III-Colon-Cancer/">FDA Approves Genentech&#39;s Tecentriq in Combination With a Fluoropyrimidine and Oxaliplatin for the Adjuvant Treatment of a Certain Type of Stage III Colon Cancer</a>
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        SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)---- $RHHBY--Genentech, a member of the Roche Group (SIX: RO, ROP; OTCQX: RHHBY), announced today that the U.S. Food and Drug Administration (FDA) has approved Tecentriq® (atezolizumab) and Tecentriq Hybreza® (atezolizumab and hyaluronidase-tqjs) in combination with a fluoropyrimidine and oxaliplatin for the adjuvant treatment of stage III deficient D...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Roche-CH1499059983">Roche</a></div>
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        <div class="me-2 text-gray">GlobeNewsWire</div>
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        <div class="me-2 text-gray">29 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/10/09/3377811/0/en/fda-approves-roche-s-tecentriq-in-combination-with-a-fluoropyrimidine-and-oxaliplatin-for-the-adjuvant-treatment-of-a-certain-type-of-stage-iii-colon-cancer.html">FDA approves Roche&#39;s Tecentriq in combination with a fluoropyrimidine and oxaliplatin for the adjuvant treatment of a certain type of stage III colon cancer</a>
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        Basel, 9 October 2026 - Roche (SIX: RO, ROP; OTCQX: RHHBY) announced today that the US Food and Drug Administration (FDA) has approved Tecentriq® (atezolizumab) and Tecentriq Hybreza® (atezolizumab and hyaluronidase-tqjs) in combination with a fluoropyrimidine and oxaliplatin for the adjuvant treatment of stage III deficient DNA mismatch repair (dMMR) colon cancer, a type of tumour characterise...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Roche-CH1499059983">Roche</a></div>
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        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">about one month ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/zealand-roches-obesity-drug-helps-patients-lose-up-92-weight-mid-stage-trial-2026-10-07/">Zealand, Roche&#39;s obesity drug helps patients lose up to 9.2% weight in mid-stage trial</a>
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        Zealand Pharma said on Wednesday its experimental drug helped people who are overweight or ​obese and have type 2 diabetes ‌lose up to 9.2% of their body weight in a mid-stage trial. The Danish company is developing it ​with Roche.
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        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">about one month ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/alector-soars-roche-licenses-parkinsons-therapy-up-127-billion-2026-10-05/">Alector soars as Roche licenses Parkinson&#39;s therapy for up to $1.27 billion</a>
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        Swiss drugmaker Roche will pay up to $1.27 billion to license Alector&#39;s experimental treatment for ​Parkinson&#39;s disease, the US biotech said ‌on Monday, sending its shares surging 72% in premarket trading.
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