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CSRWire - Teva Sets Ambitious Long-Term Environmental Goals As Part of Renewed ESG Strategy

The new 2030 goals are a key pillar of the Environmental, Social and Governance (ESG) strategy at the world’s leading generic medicine provider ....

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Teva to Host Conference Call to Discuss Fourth Quarter 2020 Financial Results and 2021 Financial Gui

TEL AVIV, Israel (BUSINESS WIRE) Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) announced today that it will issue a press release on its fourth quarter and full year 2020 financial results, as well as on its financial guidance for 2021, on Wednesday, February 10, 2021 at 7:00 a.m. ET. Following the rel. ....

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Teva to Present at the 39th Annual J.P. Morgan Healthcare Conference

Press release content from Business Wire. The AP news staff was not involved in its creation.
Teva to Present at the 39th Annual J.P. Morgan Healthcare Conference
January 7, 2021 GMT
TEL AVIV, Israel (BUSINESS WIRE) Jan 7, 2021
Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced that President & CEO Kåre Schultz will present at the 39th Annual J.P. Morgan Healthcare Conference in San Francisco, California on Wednesday, January 13, 2021. The presentation will begin at 8:20 A.M. Eastern Time.
To access a live webcast of the presentation, visit Teva’s Investor Relations website at http://ir.tevapharm.com.
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Teva and MedinCell Announce Positive Results for Registration Trial of Investigational Extended-Release Subcutaneous Injectable Risperidone for Patients with Schizophrenia

Teva and MedinCell Announce Positive Results for Registration Trial of Investigational Extended-Release Subcutaneous Injectable Risperidone for Patients with Schizophrenia
Regulatory News:
Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) and MedinCell (Euronext: MEDCL) today announced positive results for study TV46000-CNS-30072 (the RISE study The Risperidone Subcutaneous Extended-Release Study), a Phase 3 clinical trial designed to evaluate the efficacy of TV-46000/mdc-IRM (risperidone extended-release injectable suspension for subcutaneous use) as a treatment for patients with schizophrenia. Trial enrollment was open to patients 13-65 years of age. In the RISE study, patients treated with the investigational subcutaneous risperidone injection either monthly (q1M) (n=183) or once every two months (q2M) (n=179) experienced a statistically significant delay in time to relapse versus placebo (n=181), the study s primary endpoint, with p ....

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