Welcome to our dedicated page for Teva Pharm news (Ticker: TEVA), a resource for investors and traders seeking the latest updates and insights on Teva Pharm stock.
News about Teva Pharmaceutical Industries Limited (TEVA) focuses on its transformation into an innovative biopharmaceutical company, its generics and biosimilars franchise, and developments across neuroscience and immunology. Company announcements highlight progress on its Pivot to Growth strategy, including updates on branded medicines such as AUSTEDO, AJOVY and UZEDY, as well as late-stage pipeline assets.
Recent news includes clinical and regulatory milestones for AJOVY (fremanezumab-vfrm), where Phase 3 SPACE trial results in children and adolescents with episodic migraine were published in the New England Journal of Medicine. These data supported U.S. FDA approval for preventive treatment of episodic migraine in pediatric patients who meet specified criteria, adding to AJOVY’s existing indication in adults. News items provide details on trial design, efficacy outcomes, and safety profile.
Investors and followers of TEVA can also find updates on pipeline programs such as olanzapine extended-release injectable suspension (TEV-'749) for schizophrenia and the anti‑IL‑15 antibody TEV-'408 for vitiligo and celiac disease, including regulatory submissions and funding agreements. Teva’s news flow covers biosimilar approvals and collaborations, such as European Commission approvals for denosumab biosimilars PONLIMSI and DEGEVMA and the U.S. settlement and license agreement for AVT06, a proposed biosimilar to Eylea.
In addition, TEVA news features financial and capital markets events, including rating agency actions, amendments to credit facilities, quarterly earnings release dates, conference call schedules, and participation in major healthcare conferences. This mix of clinical, regulatory, strategic and financial updates makes the TEVA news page a central resource for tracking how Teva’s generics base, innovative pipeline and biosimilars portfolio contribute to its stated Pivot to Growth strategy. Users interested in TEVA stock can monitor this page for ongoing disclosures that may inform their understanding of the company’s operations and strategic direction.
Teva Pharmaceuticals presented interim results from the FINESSE study at the German Society of Neurology (DGN) Congress 2021. The study evaluates the effectiveness of fremanezumab in chronic and episodic migraine patients. Data from 574 patients indicated a 48.7% achievement of the primary endpoint—a ≥ 50% reduction in migraine days after 6 months. Additionally, significant reductions in migraine days, disability scores, and acute medication use were observed. Overall, these findings align with previous Phase III studies and highlight fremanezumab's effectiveness in real-life settings.
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Teva Pharmaceutical Industries Limited has achieved a legal victory as Judge Peter Wilson of the Superior Court in California ruled that Teva did not cause a public nuisance regarding opioid marketing in Orange County, Los Angeles County, Santa Clara County, and Oakland. The court also found that Teva did not engage in false or misleading advertising practices. Teva emphasizes the need for comprehensive settlements to support those affected by opioid addiction, while it remains committed to providing affordable medicines globally.
Teva Pharmaceuticals announced positive results from the Phase 3 RISE study evaluating TV-46000, a long-acting injectable risperidone formulation, aimed at treating schizophrenia. The study showed that TV-46000 significantly prolonged time to relapse and increased clinical stability compared to placebo. Among 544 randomized patients, relapse rates were dramatically lower, with only 9% at week 24 for TV-46000 users versus 28% for placebo. The safety profile was consistent with existing risperidone formulations, indicating potential enhancements in treatment options for patients suffering from this disorder.
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Teva Pharmaceutical Industries Ltd. (NYSE: TEVA) has initiated cash tender offers totaling up to
Teva Pharmaceutical Industries Ltd. reported third-quarter 2021 revenues of $3.9 billion, down 2% year-over-year, with a GAAP EPS of $0.26 and a non-GAAP EPS of $0.59.
Key drivers included strong sales from AJOVY® and AUSTEDO®, while lower revenues from COPAXONE® impacted results. Teva reaffirmed its full-year guidance, anticipating net revenues of $16.0 - $16.4 billion and adjusted EBITDA of $4.8 - $5.1 billion. Cash flow from operations was $529 million with $795 million in free cash flow, reflecting efficient cash management.
Teva Pharmaceutical Industries Ltd. (NYSE: TEVA) announced a collaboration with MODAG GmbH to exclusively license and develop the small molecule candidate Anle138b, targeting neurological disorders like multiple system atrophy (MSA) and Parkinson’s disease (PD). The agreement allows Teva to develop and commercialize Anle138b and related compound Sery433, following favorable Phase 1 study results. The collaboration aims to address unmet medical needs in neurodegenerative diseases, potentially impacting thousands of patients annually.
Teva Pharmaceuticals presented new analyses from the COBRA study at the 37th Congress of the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS). The study, which included data from 99 mothers with multiple sclerosis treated with COPAXONE® (glatiramer acetate) during pregnancy and breastfeeding, found no safety concerns for infants. Specifically, there were no adverse effects on hospitalizations, antibiotic treatments, developmental delays, or growth during the first 18 months. This research addresses significant medical needs concerning treatment safety for women with MS.
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