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  • Lume Meso Design And Rationale Of The Phase Iii Part Of A Placebo Controlled Study Of Nintedanib And Pemetrexed Cisplatin Followed By Maintenance Nintedanib In Patients With Unresectable Malignant Pleural Mesothelioma Semantic Scholar
  • Bevacizumab Plus Cisplatin Pemetrexed Then Bevacizumab Alone For Unresectable Malignant Pleural Mesothelioma A Japanese Safety Study Nakano Asia Pacific Journal Of Clinical Oncology Wiley Online Library

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There are five trial sites within the uk.

Sutton lawn astro. The phase 3 trial had slightly different inclusion criteria compared to the positive nintedanib randomized phase 2specifically excluding sarcomatoid or biphasic mpm subtypes 1520 of mpm. It stops signals that cancer cells use to divide and grow. Nintedanib is a type of targeted drug called a cancer growth blocker.

And 10 in the us including. See if nintedanib delays or stops the mesothelioma coming back after chemotherapy. The study initiated by boehringer ingelheim is exploring the use of nintedanbi in treating.

In this trial some people have nintedanib. A phase 3 trial is recruiting 450 participants at clinics worldwide to test whether nintedanib used in combination with the standard chemotherapy drugs alimta pemetrexed and platinol cisplatin in patients with a certain type of lung cancer achieves better results compared to chemotherapy alone. The sponsor claimed that the phase 2 study failed to show any effect in this subpopulation contrary to the effect observed in the epithelioid subtype.

Serious adverse events were reported in 44 of the nintedanib group. The clinical trial which is still accepting new patients has moved into phase iii with an expected completion of oct. And some have a dummy drug placebo.

Boehringer ingelheims phase 2 clinical trial investigating nintedanib in malignant pleural mesothelioma showed improvements in both progression free and overall survival compared to treatment with chemotherapy alone. Only patients with the epithelioid subtype of mesothelioma are eligible. The overall survival benefit was 183 months against 142 months.

The main aims of the trial are to.

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