Company Update (NASDAQ:EXEL): European CHMP Adopts Positive Opinion for Exelixis, Inc.’s Cobimetinib in Combination with Vemurafenib for the Treatment of Advanced Melanoma

Exelixis, Inc. (NASDAQ:EXEL) announced that the European Medicines Agency’s Committee for Medical Products for Human Use (CHMP) has adopted a positive opinion of the Marketing Authorization Application for cobimetinib, a selective MEK inhibitor discovered by Exelixis, in combination with vemurafenib for the treatment of BRAF V600 mutation-positive unresectable or metastatic melanoma. The CHMP’s positive opinion will now be reviewed by the European Commission, which has the authority to approve medicines for the European Union. The European Commission is expected to release its final decision regarding the approval of the combination of cobimetinib and vemurafenib by the end of 2015.

“The CHMP’s positive opinion on cobimetinib for use in combination with vemurafenib is an important milestone in bringing this new therapeutic option to patients in Europe,” said Michael M. Morrissey, Ph.D., president and chief executive officer of Exelixis. “We congratulate Genentech and Roche on this latest milestone in the European regulatory process. We also look forward to the regulatory decision anticipated this year in the United States, where we are fully prepared to co-promote cobimetinib with our partners.”

The CHMP’s recommendation is based on data from coBRIM, the international, randomized double-blind controlled phase 3 pivotal trial evaluating cobimetinib in combination with vemurafenib in previously untreated patients with unresectable locally advanced or metastatic melanoma harboring a BRAF V600 mutation.

The combination of cobimetinib and vemurafenib recently received its first approval inSwitzerland, where cobimetinib is marketed as Cotellic™.

The coBRIM trial was conducted by Roche and Genentech, a member of the Roche Group. Genentech filed a New Drug Application (NDA) for cobimetinib in the United States, for which the Prescription Drug User Fee Act action date is November 11, 2015. (Original Source)

Shares of Exelixis closed yesterday at $6.20. EXEL has a 1-year high of $6.81 and a 1-year low of $1.26. The stock’s 50-day moving average is $5.87 and its 200-day moving average is $4.12.

On the ratings front, Exelixis has been the subject of a number of recent research reports. In a report issued on September 18, William Blair analyst John Sonnier reiterated a Buy rating on EXEL. Separately, on July 20, Cowen’s Eric Schmidt upgraded the stock to Buy .

According to, which ranks over 7,500 financial analysts and bloggers to gauge the performance of their past recommendations, John Sonnier and Eric Schmidt have a total average return of 21.7% and 34.1% respectively. Sonnier has a success rate of 63.6% and is ranked #199 out of 3764 analysts, while Schmidt has a success rate of 52.9% and is ranked #52.

Exelixis Inc is a biotechnology company that develops small molecule therapies for the treatment of cancer.

Stay Ahead of Everyone Else

Get The Latest Stock News Alerts