Communiqués Roche Holding AG London S.E.

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CH0012032048

Produits pharmaceutiques

Marché Fermé - London S.E. 17:20:00 26/06/2026 Varia. 5j. Varia. 1 janv.
323,90 CHF 0,00 % Graphique intraday de Roche Holding AG 0,00 % -1,29 %

Communiqués

18/06 FDA Accepts Supplemental Biologics License Application for Genentech’s Lunsumio and Polivy Combination for People With Relapsed or Refractory Large B-Cell Lymphoma BU
11/06 FDA Grants Priority Review for Genentech’s Tecentriq for a Certain Type of Stage III Colon Cancer BU
04/06 Roche rapidly develops a PCR test for Ebola within six days as rare Bundibugyo virus drives urgent need for detection PR
02/06 FDA Accepts New Drug Application for Genentech’s Giredestrant in ER-Positive Early-Stage Breast Cancer, the First and Only Oral SERD With Positive Phase III Results in the Curative Setting BU
01/06 Genentech to Present New Data Advancing Its Obesity Portfolio at the American Diabetes Association’s 2026 Scientific Sessions BU
19/05 Genentech to Present New Data at ASCO 2026, Reinforcing Giredestrant's Potential to Transform the Treatment Paradigm in Early Breast Cancer BU
15/05 FDA Approves Genentech’s Tecentriq for Adjuvant Muscle-Invasive Bladder Cancer With ctDNA-Guided Treatment BU
30/04 Genentech to Present Extensive Data Showcasing Its Industry-Leading Ophthalmology Portfolio at ARVO 2026 BU
24/04 Genentech Partners With Comedy Icon Damon Wayans and diaTribe to Address Diabetes-Related Vision Loss With ‘All Eyes on DME’ Campaign BU
22/04 Roche's ENSPRYNG (satralizumab) reduces risk of relapses by 68% demonstrating potential to become first treatment for MOGAD AQ
22/04 Genentech’s Fenebrutinib Significantly Reduced Relapses Versus Standard of Care to Approximately One Every 17 Years in RMS BU
21/04 Genentech’s Enspryng (Satralizumab) Reduces Risk of Relapses by 68% Demonstrating Potential to Become First Treatment for MOGAD BU
21/04 CORRECTING and REPLACING FDA Accepts Application for Genentech’s Gazyva for the Treatment of the Most Common Form of Lupus BU
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