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F Hoffmann-La Roche Ltd: Eight-year data from APHINITY study show Roche s Perjeta-based regimen continues to reduce the risk of disease returning for people with HER2-positive early breast cancer

Greatest benefit continued to be seen in people who are at a high risk of recurrence (those with lymph node-positive disease)With longer follow-up, treatment effect continues to be seen regardless of hormone

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FDA Approves J&J s Darzalex Faspro for Sixth Multiple Myeloma Indication

FDA Approves J&J s Darzalex Faspro for Sixth Multiple Myeloma Indication
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Halozyme enhanzeCraig tendlerDarzalex fasproMeletiosa dimopoulosGlobal medical affairsSlate developmentKapodistrian university of athens school medicineDrug administrationDepartment of clinical therapeuticsJanssen research developmentUnited states foodJanssen pharmaceutical companiesClinical therapeuticsKapodistrian universityAthens schoolJanssen biotech

Collaboration to develop ultra-long acting medicines for HIV

Collaboration to develop ultra-long acting medicines for HIV
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Halozyme enhanzeDevelopment agreementInfectious disease vaccine research centerNational institute of allergyNational institutes of healthHalozyme therapeutics incHalozyme therapeuticsCooperative researchNational instituteViiv healthcareNational institutesதொற்று நோய் தடுப்பூசி ஆராய்ச்சி மையம்தேசிய நிறுவனம் ஆஃப் ஒவ்வாமைதேசிய நிறுவனங்கள் ஆஃப் ஆரோக்கியம்கூட்டுறவு ஆராய்ச்சிதேசிய நிறுவனம்

European Commission approves Roche s Phesgo (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection) for people with HER2-positive breast cancer – IT Business Net

European Commission approves Roche s Phesgo (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection) for people with HER2-positive breast cancer – IT Business Net
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San antonioUnited statesNathalie meetzHalozyme enhanzeLevi garrawayDaniel grotzkyPatrick barthKarsten kleineDrug delivery technologyEuropean commissionDrug administrationHead of global product developmentRoche groupPharmaceuticals industrySafety of subcutaneous administration theRoche group media relations

F Hoffmann-La Roche Ltd: European Commission approves Roche s Phesgo (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection) for people with HER2-positive breast cancer

F. Hoffmann-La Roche Ltd: European Commission approves Roche s Phesgo (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection) for people with HER2-positive breast cancer 1,2,3 administered under the skin in just minutes compared to hours with intravenous ( IV) infusion of Perjeta plus Herceptin 4,5,6 Approval is based on results from the pivotal phase III FeDeriCa trial, which showed that Phesgo delivered non-inferior 7 Basel, 23 December 2020 - Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the European Commission has approved Phesgo , a fixed-dose combination of Perjeta (pertuzumab) and Herceptin (trastuzumab) with hyaluronidase, administered by subcutaneous (SC; under the skin) injection for the treatment of early and metastatic HER2-positive breast cancer.

San antonioUnited statesNathalie meetzHalozyme enhanzeLevi garrawayDaniel grotzkyJon kaspar bayardKarl mahlerSabine borngrGerard tobinBruno eschliBirgit masjostLisa tuomiLoren kalmPatrick barthKarsten kleine