Communiqués Teva Pharmaceutical Industries Ltd (ADR) Nasdaq

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US8816242098

Produits pharmaceutiques

Temps réel estimé Cboe BZX 21:59:59 25/08/2026			Varia. 5j.	Varia. 1 janv.
38,11 ^USD	0,00%		0,00%	-

19/08	Aurinia règle son litige sur les brevets avec Teva ; le titre progresse après-bourse	MT
19/08	Teva Pharmaceutical Industries : un dirigeant cède pour 680 291 $ d'actions, selon un document de la SEC	MT

Communiqués

20/08	U.S. FDA Accepts Teva's New Drug Application (NDA) and Grants Priority Review for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Patients with Tourette Syndrome	AQ
19/08	U.S. FDA Accepts Teva’s New Drug Application (NDA) and Grants Priority Review for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Patients with Tourette Syndrome	GL
11/08	Moody’s Ratings Upgrades Teva to Investment Grade, Reflecting the Ongoing Execution of Pivot to Growth Strategy	GL
29/07	Teva Delivers Strong Q2 Results and Raises Outlook for All Three Key Innovative Brands, Reflecting Continued Execution of Its Pivot to Growth Strategy	GL
10/07	Teva and Polpharma Biologics Announce Global Licensing Agreement for a Biosimilar Candidate to Ocrevus for Multiple Sclerosis	AQ
10/07	Teva et Polpharma Biologics annoncent la signature d’un accord de licence mondial portant sur un candidat biosimilaire à l’Ocrevus® (ocrelizumab) destiné au traitement de la sclérose en plaques	BU
09/07	Teva and Polpharma Biologics Announce Global Licensing Agreement for a Biosimilar Candidate to Ocrevus® (ocrelizumab) for Multiple Sclerosis	BU
09/07	Teva and Polpharma Biologics Announce Global Licensing Agreement for a Biosimilar Candidate to Ocrevus® (ocrelizumab) for Multiple Sclerosis	GL
07/07	Teva to Advance Its Anti-IL-15 Antibody, Designed for Quarterly Dosing, Into Phase 2b Development in Vitiligo, Following Encouraging Phase 1b Results	GL
18/06	Teva Releases Q2 2026 Aide Memoire	GL
18/06	Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome	GL
18/06	Teva to Host Conference Call to Discuss Second Quarter 2026 Financial Results on July 29, 2026 at 8 a.m. ET	GL
10/06	Teva Closes Acquisition of Emalex Biosciences, Strengthening Late-Stage Neuroscience Pipeline and Advancing Pivot to Growth Strategy	GL
08/06	Teva’s Data on AUSTEDO® (deutetrabenazine) tablets and AUSTEDO XR® (deutetrabenazine) extended-release tablets Highlight Long-Term Advances in Tardive Dyskinesia Treatment and Care	GL
08/06	Teva Presents New Data on AUSTEDO tablets and AUSTEDO XR extended-release tablets that Show Patient- and Caregiver-Reported Improvements in Huntington's disease Chorea	AQ
05/06	Teva Presents New Data on AUSTEDO® (deutetrabenazine) tablets and AUSTEDO XR® (deutetrabenazine) extended-release tablets that Show Patient- and Caregiver-Reported Improvements in Huntington's Disease Chorea	GL
05/06	Teva Expands European biosimilars portfolio with launch of AHZANTIVE biosimilar to Eylea	AQ
04/06	Teva Expands European biosimilars portfolio with launch of AHZANTIVE® (aflibercept) biosimilar to Eylea®	GL
01/06	Teva to Present at the Goldman Sachs Global Healthcare Conference	GL
21/05	The European Medicines Agency Accepts Teva’s Marketing Authorization Application for Olanzapine Long-Acting Injectable (TEV-‘749) for the Treatment of Schizophrenia in Adults	GL
18/05	Fitch Upgrades Teva to Investment Grade Amid Pivot to Growth Execution	GL
18/05	Teva Study Finds Only 23% of Younger Adults with Mood Disorders and Tardive Dyskinesia (TD) Symptoms Are Formally Diagnosed with TD Despite Widespread Impact	GL
04/05	Teva to Present at the BofA Securities Health Care Conference	GL
30/04	Teva's 2025 Healthy Future Report Highlights Environmental and Access to Medicines Progress, Including Meeting All Sustainability-Linked Bond Targets	AQ
30/04	Teva’s 2025 Healthy Future Report Highlights Environmental and Access to Medicines Progress, Including Meeting All Sustainability-Linked Bond Targets	GL