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Temps Différé Deutsche Boerse AG Autres places de cotation 08:12:54 27/06/2024			Varia. 5j.	Varia. 1 janv.
13 ^EUR	-0,76 %		+0,78 %	-5,11 %

12:39	La FDA américaine refuse d'approuver le médicament anticancéreux "missile guidé" de Merck-Daiichi	RE
24/06	La Cour suprême des États-Unis donne aux entreprises pharmaceutiques une chance de contrecarrer les poursuites pour financement du terrorisme	RE

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A New Wave Of ERISA Class Actions?: Some Employer/Fiduciary Implications Of Lewandowski V. Johnson & Johnson (Podcast)	16:12	AQ
Johnson & Johnson Reaches 50 Million Children Through Sight For Kids Program	25/06	AQ
Johnson & Johnson completes acquisition of Proteologix, Inc.	24/06	AQ
Johnson & Johnson Completes Acquisition of Proteologix, Inc.	21/06	BU
Health Authority Warns of Brain Risks From Pseudoephedrine Medications	21/06	AQ
Johnson & Johnson submits application to U.S. FDA seeking approval of TREMFYA® (guselkumab) for the treatment of moderately to severely active Crohn's disease	20/06	PR
More than 60 Law Firms Oppose J&J Prepack Bankruptcy Scheme	20/06	BU
TREMFYA® (guselkumab) studies underscore its potential to be the only IL-23 inhibitor to offer both subcutaneous and intravenous induction	20/06	PR
Johnson & Johnson - Subcutaneous amivantamab Biologics License Application submitted to U.S. FDA for patients with EGFR-mutated non-small cell lung cancer	18/06	AQ
Beasley Allen and Levin Papantonio: Leading Law Firms Seek Protection for Future Victims of Johnson & Johnson Talc Products	17/06	BU
J&J commits five-year investment in Italian medicine manufacturing	17/06	AQ
Johnson & Johnson - Late-breaking results show nipocalimab significantly improves Sjogren's disease activity in a Phase 2 study	17/06	AQ
Johnson & Johnson - TALVEY demonstrates highly durable, longer-term responses in patients with relapsed or refractory multiple myeloma	17/06	AQ
Late-breaking results show nipocalimab significantly improves Sjögren's disease activity in a Phase 2 study	15/06	PR
Johnson & Johnson : Findings from landmark RESONATE 2 study confirm sustained survival benefit of IMBRUVICA® (ibrutinib) for first line chronic lymphocytic leukaemia treatment with up to 10 years follow up	14/06	PU
Johnson & Johnson : Updated Phase 2 CAPTIVATE study results demonstrate sustained clinical benefit of fixed duration IMBRUVICA® (ibrutinib) plus venetoclax as first line treatment for patients with chronic lymphocytic leukaemia, including those with high risk disease	14/06	PU
That's Stentertainment	13/06	AQ
Johnson & Johnson : to Participate in the Goldman Sachs 45th Annual Global Healthcare Conference Press Release	12/06	PU
Talc Plaintiffs File Motion for Temporary Restraining Order to Limit Johnson & Johnson’s Use of Bankruptcy Strategy	12/06	BU
Johnson & Johnson agrees to pay $700M to settle talcum lawsuit with dozens of states	12/06	AQ

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Joseph Wolk, CFO de J&J: Perte d'exclusivité de son médicament phare

Le 23 janvier 2024 à 18:30