Germany
Spain
Japan
United States
This website is an international information resource intended for international healthcare professionals outside the United States of America (US) and the United Kingdom (UK) who are interested in information about Boehringer Ingelheim oncology.
While the Internet serves a global community, the pharmaceutical industry is subject to country-specific regulatory considerations. This means that compound status or the registration status and approved product labels of the products described within this website may not be the same in different countries.
Information about approved products on this website is derived from the Summary of Product Characteristics (SPC) for each product in the EU. It is not country-specific and may vary from the approved label in the country where you are located. Please refer to your local Prescribing Information for full details.
By clicking on the link below you are declaring and confirming that you are a healthcare professional outside the United States of America and the United Kingdom and have read and understood this disclaimer.
This site uses cookies to improve your browsing experience. By using this site, you agree to their use. Cookie Policy
Phase II LUME-Meso study of first-line nintedanib plus chemotherapy in malignant pleural mesothelioma: additional efficacy analyses
Popat S, Novello S, Nowak A, Grosso F, Steele N, Greillier L, John T, Leighl NB, Reck M, Pavlakis N, Sørensen JB, Planchard D, Ceresoli GL, Hughes B, Mazières J, Socinski MA, von Wangenheim U, Barrueco J, Morsli N and Scagliotti G
This poster is presented for scientific education and its content may go beyond the scope of the current market authorization for nintedanib in Canada.
Related articles
Learn more about the science behind this presentation in the papers and other materials below
Nintedanib is being investigated in malignant pleural mesothelioma (MPM) and is not approved for this use. The efficacy and safety of nintedanib in MPM have not been established.
Nintedanib is approved in the EU under the brand name VARGATEF® for use in combination with docetaxel in adult patients with locally advanced, metastatic or locally recurrent NSCLC of adenocarcinoma tumour histology after first-line chemotherapy. For the full list of country-specific information please click here. Nintedanib is not approved in other oncology indications.
© 2018 Boehringer Ingelheim International GmbH. All rights reserved.
Last updated: May 2018