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 announced new data on AJOVY (fremanezumab) at the American Headache Society meeting, highlighting clinical and real-world efficacy for treating migraines. The presentation includes a 12-month extension study from the HALO clinical program, addressing both episodic and chronic migraines. Key findings show that patients experienced statistically significant reductions in migraine days, with notable results among those with comorbid conditions like depression and anxiety. AJOVY remains the only long-acting anti-CGRP injection approved in the US.
Teva Pharmaceuticals announced 11 presentations on AJOVY® (fremanezumab-vfrm) at the 2021 American Headache Society Annual Meeting from June 3-6. The research highlights AJOVY's effectiveness in migraine treatment, showcasing clinical data spanning 15 months. Key findings include the drug's significant impact on patients with comorbid conditions like depression and anxiety. AJOVY is available in single-dose injections and is indicated for preventive migraine treatment in adults. For further information, details can be found on Teva's website.
Teva Pharmaceuticals has launched the first generic version of THIOLA® (tiopronin) tablets in the U.S., aimed at preventing cystine kidney stone formation in adults and children aged 9 and above. The medication is intended for patients unresponsive to standard treatments such as increased fluid intake and dietary changes. Teva, known for its extensive portfolio of over 550 generic medicines, holds a leading market position in generics with around 1 in 11 prescriptions in the U.S. filled with its products. The company continues to focus on expanding its generic offerings, with about 100 additional products pending approval.
Teva Pharmaceuticals launched the "It’s Not OK – It’s TD" campaign to raise awareness about tardive dyskinesia (TD) and promote AUSTEDO® (deutetrabenazine) as a treatment option. The campaign encourages patients to discuss their symptoms with healthcare providers instead of coping silently. TD can affect 1 in 4 individuals on certain mental health medications, leading to significant physical and emotional impacts. Clinical studies show AUSTEDO significantly reduces TD symptoms, with sustained improvement over 145 weeks. Teva also offers resources and financial assistance to support patients during treatment.
Teva Pharmaceuticals has announced the presentation of two e-posters at the ATS International Conference from May 14-19, 2021. One poster focuses on the increased use of short-acting beta-agonist (SABA) in patients with poorly controlled asthma using the ProAir® Digihaler®. The second addresses real-world uncontrolled COPD therapy. These findings underscore Teva's commitment to improving respiratory disease treatments, utilizing data from their digital inhaler to inform patient management.
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Teva Pharmaceuticals has launched its generic Erythromycin tablets in 250 mg and 500 mg strengths, a therapeutic equivalent to Arbor Pharmaceuticals' reference drug. These tablets are used to treat several bacterial infections and prevent rheumatic fever in penicillin-allergic patients. Teva, with a robust portfolio of nearly 550 generic medicines, leads in FDA-approved generics and holds approximately 100 first-to-file opportunities. Annual sales for Erythromycin in the U.S. exceed $49 million, indicating significant market potential for Teva's new offering.
Teva Pharmaceuticals announced new data from a 3-year study of AUSTEDO® (deutetrabenazine) for tardive dyskinesia (TD), to be presented at the 2021 APA Virtual Annual Meeting (May 1-3). This study investigates long-term safety, quality of life (QoL), and patient outcomes in 337 patients. Results show that 79.8% reported at least one adverse event, with low incidence rates. QoL improvements were noted with significant scores change over 145 weeks. AUSTEDO is indicated for both TD and chorea associated with Huntington’s disease.
Teva Pharmaceuticals has launched the first generic isotretinoin capsules (10 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg) in the U.S. for treating severe nodular acne in non-pregnant patients aged 12 and older. This introduction adds to Teva's robust portfolio, which includes over 550 generic medicines. Isotretinoin capsules, with annual sales exceeding $158 million, offer an essential option for patients unresponsive to conventional therapies. Teva's generics division continues to lead in first-to-file opportunities, further solidifying its market presence.
Teva Pharmaceutical Industries Ltd. (TEVA) reported Q1 2021 revenues of $3,982 million, a 9% decline from Q1 2020. Profitability improved, with net debt reduced to $23.2 billion. Key products like Truxima® and AUSTEDO® showed growth, while COPAXONE revenues fell significantly in both North America and Europe. GAAP net income increased to $77 million, with EPS at $0.07. However, non-GAAP net income dropped to $699 million and diluted EPS to $0.63, reflecting a 12% decrease in adjusted EBITDA. Teva maintains a financial leverage of 69%.
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