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Roche/Genentech seek FDA nod for cobimetinib+Zelboraf in melanoma

This article was originally published in Scrip

Executive Summary

Roche US subsidiary Genentech is seeking US approval to market cobimetinib (GDC-0973, XL518) in combination with the companies’ already approved drug Zelboraf (vemurafenib) for patients with BRAF V600 mutation-positive advanced melanoma.

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