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Teva Pharma Aktie (ADR) News

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WKN:  883035 ISIN:  US8816242098 US-Symbol:  TEVA Branche:  Pharmazeutika Land:  Israel
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Teva Pharmaceutical Aktie (ADR) News

03.03.26 - GlobeNewswire
Teva and Blackstone Life Sciences Announce $400 Million Strategic Growth Capital Agreement to Advance duvakitug
Blackstone Life Sciences will provide $400 million to support development of duvakitug, a human monoclonal antibody targeting TL1A Duvakitug is currently in phase 3 clinical ...
24.02.26 - GlobeNewswire
Teva to Present at the Upcoming Investor Conferences in March
PARSIPPANY, N.J. and TEL AVIV, Israel, Feb. 24, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced that Richard Francis, ...
20.02.26 - GlobeNewswire
U.S. Food and Drug Administration (FDA) Accepts Teva’s New Drug Application (NDA) for Olanzapine Extended-Release Injectable Suspension (TEV-'749) for the Once-Monthly Treatment of Schizophrenia in Adults
Olanzapine long-​acting injectable (LAI) suspension (TEV-'749) has the potential to offer the efficacy of olanzapine in a once-​monthly, subcutaneous formulation 1 If approved, TEV-...
17.02.26 - GlobeNewswire
Teva and Sanofi’s duvakitug phase 2b maintenance data demonstrated clinically meaningful durable efficacy in ulcerative colitis and Crohn’s disease
In the RELIEVE UCCD LTE phase 2b study, duvakitug showed robust, durable efficacy for an additional 44 weeks in UC and CD patients who had responded after 14 weeks of ...
28.01.26 - GlobeNewswire
Teva Innovative Portfolio and Consistent Execution of Pivot to Growth Strategy Deliver Third Consecutive Year of Growth; Pipeline Positioned to Unlock Significant Value Potential
Teva delivers 3 consecutive years of growth - 2025 revenues of $17.3 billion, an increase of 4% year-​over-year (YoY) in U.S. dollars, or 3% in local currency (LC) terms, compared to ...
27.01.26 - GlobeNewswire
Will Forte Teams Up with Teva to Get Real About Huntington’s Disease with ‘Honestly HD’
Actor and comedian, Will Forte, opens up about his brother-​in-law's journey with Huntington’s disease (HD) and chorea through Teva’s Honestly HD program HD is a rare, ...
26.01.26 - wallstreetONLINE Redaktion
Streit um Diabetes-Markt: Milliarden-Blockbuster unter Beschuss: Klage könnte Novo teuer zu stehen kommen
Eine Klage wirft Novo Nordisk vor, günstige Generika jahrelang blockiert zu haben. Im Zentrum steht ein Deal und der Milliardenumsatz eines Diabetesmittels.Der dänische ...
14.01.26 - GlobeNewswire
AJOVY® (fremanezumab-vfrm) Significantly Reduced Monthly Migraine and Headache Days in Children and Adolescents with Episodic Migraine Compared to Placebo in the SPACE Trial; Results Published in New England Journal of Medicine
AJOVY demonstrated efficacy and a consistent safety profile in the SPACE trial, making it the first and only calcitonin gene-​related peptide (CGRP) antagonist treatment option for ...
12.01.26 - GlobeNewswire
Teva to Present at the 44th Annual J.P. Morgan Healthcare Conference: Pivot to Growth Strategy Delivering Growth and Transforming through Innovation
Richard Francis, Teva's President and CEO, will present at the 44th Annual J.P. Morgan Healthcare Conference on Tuesday, January 13, 2026, at 8:15 A.M. Pacific Time (11:15 A.M. ...
11.01.26 - GlobeNewswire
Teva and Royalty Pharma Enter Agreement to Accelerate Development of Potential Treatment for Vitiligo
Royalty Pharma to provide up to $500 million, including $75 million for Phase 2b funding and a Royalty Pharma option for an additional $425 million to support Teva’s anti-IL-15 ...
05.01.26 - GlobeNewswire
Teva to Present at the 44th Annual J.P. Morgan Healthcare Conference
TEL AVIV, Israel, Jan. 05, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced that Richard Francis, Teva's President and ...
24.12.25 - GlobeNewswire
S&P Global Ratings Upgrades Teva to ‘BB+’ Amid Strong Execution of Pivot to Growth Strategy; Moody's Ratings Agency Revises Outlook to Positive
The two updates underscore Teva’s strong execution of its Pivot to Growth strategy and commitment to financial discipline. Moody's affirmed Teva's B1a rating and revised Teva's ...
19.12.25 - GlobeNewswire
Alvotech and Teva Secure U.S. Settlement Date for AVT06, a Proposed Biosimilar to Eylea®
According to the settlement agreement, the proposed biosimilar to Eylea ® (aflibercept) can be marketed in the U.S., if approved by the FDA, in the fourth quarter of 2026, or earlier ...
12.12.25 - GlobeNewswire
Teva to Host Conference Call to Discuss Fourth Quarter 2025 Financial Results at 8 a.m. ET on January 28, 2026
TEL AVIV, Israel, Dec. 12, 2025 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) announced today that it will issue a press release on its fourth ...
12.12.25 - GlobeNewswire
Teva Releases Q4 2025 Aide Memoire
TEL AVIV, Israel, Dec. 12, 2025 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) announced today that its Q4 2025 Aide Memoire is available on ...
09.12.25 - GlobeNewswire
Teva Pharmaceuticals Submits New Drug Application to FDA for Olanzapine Extended-Release Injectable Suspension (TEV-'749) for the Once-Monthly Treatment of Schizophrenia in Adults
Olanzapine long-​acting injectable (LAI) has the potential to offer the efficacy of olanzapine in a once-​monthly, subcutaneous formulation, for a broad patient population 1 Olanzapine ...
04.12.25 - dpa-AFX
KORREKTUR/Pharmabranche: Engpässe bei Kinderarzneien sind gesunken
Bisherige Schritte der Politik gegen Arznei-​Engpässe in Deutschland haben aus Sicht des Pharmaverbands Pro Generika nur begrenzt geholfen. Zwar habe sich die Versorgung bei ...
04.12.25 - dpa-AFX
Pharmabranche: Keine Entspannung bei Engpässen von Kinderarzneien
Bisherige Schritte der Politik gegen Arznei-​Engpässe in Deutschland haben aus Sicht des Pharmaverbands Pro Generika nur begrenzt geholfen. Zwar habe sich die Versorgung bei ...
26.11.25 - GlobeNewswire
Teva erhält Zulassung der Europäischen Kommission für PONLIMSI® (Denosumab), ein Biosimilar zu Prolia®, und DEGEVMA® (Denosumab), ein Biosimilar zu Xgeva®
Aufgrund der positiven Stellungnahmen des Ausschusses für Humanarzneimittel (CHMP) hat die Europäische Kommission die Zulassungen für die Biosimilars PONLIMSI und ...
25.11.25 - GlobeNewswire
Teva receives European Commission approvals for PONLIMSI® (denosumab) Biosimilar to Prolia® and DEGEVMA® (denosumab) Biosimilar to Xgeva®
Following the positive opinions of the Committee for Medicinal Products for Human Use (CHMP ) , the European Commission has granted marketing authorizations for Teva’s ...

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