Teva Pharm (TEVA) Stock News

Teva Pharmaceuticals (NYSE: TEVA) announced that the FDA has granted Fast Track designation for emrusolmin (TEV-56286), their investigational treatment for Multiple System Atrophy (MSA). The drug, currently in Phase 2 development, targets the alpha synuclein protein involved in MSA pathogenesis.

Emrusolmin, developed in collaboration with MODAG GmbH, previously received Orphan Drug designation in 2022. The Fast Track status aims to expedite the development and review process for this potential treatment of MSA, a rare and progressive neurodegenerative disorder with no current cure or disease-modifying treatments.

Teva Pharmaceutical Industries Ltd. (NYSE:TEVA) has announced that its President and CEO, Richard Francis, will participate in two major healthcare investor conferences in September 2025. Francis will present at the Morgan Stanley 23rd Annual Global Healthcare Conference on September 9 at 8:30 A.M. ET and at the BofA Global Healthcare Conference 2025 in London on September 24 at 9:00 A.M. BST (4:00 A.M. ET).

Investors can access live webcasts of both presentations through Teva's Investor Relations website, with archived versions available within 24 hours after each live discussion.

Teva Pharmaceuticals (NYSE: TEVA) has received FDA approval and launched the first-ever generic version of Saxenda® (liraglutide injection), a GLP-1 receptor agonist for weight loss. This groundbreaking generic is indicated for adults with obesity or overweight with weight-related medical conditions, and pediatric patients aged 12-17 years weighing over 60 kg with obesity.

The approval marks Teva's fifth first-to-market generic entry this year, reinforcing their position as a Generics Powerhouse. The reference drug Saxenda® reported annual sales of $165 million as of June 2025, representing a significant market opportunity. The medication is designed to be used in combination with reduced calorie diet and increased physical activity for long-term weight management.

Teva Pharmaceuticals (NYSE: TEVA) has received FDA approval for an expanded indication of AJOVY® (fremanezumab-vfrm) for preventive treatment of episodic migraine in children and adolescents aged 6-17 years weighing 45kg or more. This milestone makes AJOVY the first and only CGRP antagonist approved for pediatric episodic migraine prevention.

The treatment, which can be administered monthly either in-office or at home, addresses a significant medical need, as 1 in 10 children and adolescents in the U.S. suffer from migraine. This expansion builds upon AJOVY's initial U.S. approval in 2018 for adult patients, demonstrating Teva's commitment to broadening access to neuroscience therapies across age groups.

Teva Pharmaceuticals (NYSE:TEVA) reported strong Q2 2025 results, marking its 10th consecutive quarter of year-over-year growth. The company achieved revenues of $4.2 billion and increased its 2025 outlook for key innovative products. Notable highlights include AUSTEDO revenues of $498 million (+19%), AJOVY reaching $155 million (+31%), and UZEDY at $54 million (+120%).

The company reported GAAP EPS of $0.24 and Non-GAAP EPS of $0.66, a 9% increase year-over-year. Free cash flow grew 47% to $476 million. Teva remains on track to achieve a 30% operating profit margin by 2027 through its transformation programs, targeting ~$700 million in net savings.

Teva Pharmaceutical Industries (NYSE:TEVA) has released its Q2 2025 Aide Memoire document, which is now accessible on the company's investor relations website. The document serves as a financial modeling aid for analysts and investors, incorporating historical performance data, management's business outlook, and selected third-party information.

Teva Pharmaceutical Industries Ltd. (NYSE:TEVA) has scheduled its second quarter 2025 financial results announcement for July 30, 2025. The company will release its financial results at 7:00 a.m. ET, followed by a conference call and live webcast at 8:00 a.m. ET.

Investors and interested parties can participate by registering in advance to obtain local or toll-free phone numbers. The webcast will be accessible through Teva's investor relations website, with a replay available within 24 hours after the call.

Teva Pharmaceuticals (TEVA) announced final results from its two-year PEARL Phase 4 real-world study of AJOVY (fremanezumab) for migraine prevention. The study, presented at EAN 2025 Congress, demonstrated sustained effectiveness in reducing migraine frequency, duration, and severity in both chronic and episodic migraine patients. The study of 1,140 patients showed that over 66% of episodic migraine patients and 51.6% of chronic migraine patients achieved ≥50% reduction in Monthly Migraine Days (MMD) during the first 6 months, with benefits sustained over 24 months. Notable outcomes include high injection adherence rates (~90%) and strong study completion rate (75%). The drug maintained a favorable safety and tolerability profile throughout the study period, consistent with previous trials.

Teva Pharmaceutical (NYSE: TEVA) and Fosun Pharma have formed a strategic partnership to develop TEV-56278, an anti-PD1-IL2 ATTENUKINE therapy currently in Phase 1 trials for various cancers including melanoma. Under the agreement, Fosun Pharma receives exclusive rights to develop, manufacture, and commercialize TEV-56278 in mainland China, Hong Kong, Macau, Taiwan, and select Southeast Asian countries, while Teva maintains rights for the rest of the world. TEV-56278, developed using Teva's ATTENUKINE technology, represents a novel approach to cancer immunotherapy by selectively delivering IL-2 to PD-1+ T cells, potentially offering high efficacy and low toxicity. The partnership aims to accelerate clinical data generation, with Teva leveraging Fosun Pharma's data in other regions.