- May 31 -- Abstract #4000: K-Ras mutational status effect on progression-free survival and response rate outcomes for patients in phase III OPUS trial
- June 1 -- Abstract #2: K-Ras mutational status effect on progression-free survival and response rate outcomes for patients from phase III CRYSTAL study
German drugmaker Merck KGaA said Friday that its cancer drug Erbitux received a positive opinion as a first-line treatment for colorectal cancer from the committee that advises European drug regulators. The Committee for Medicinal Products for Human Use (CHMP) advised the European Medicines Agency to approve an expanded label for Erbitux (in combination with chemotherapy or in certain cases as a single agent) to include metastatic colorectal cancer (mCRC) in previously untreated patients with KRAS wild-type tumors. Roughly 65% of colon cancer patients have KRAS wild-type tumors according to the company. The committee also recommended its approval as a single agent in patients who are intolerant of chemotherapy regimens. Merck KGaA said the submission to European regulators was partially supported by data collected from the so-called Crystal and OPUS trials. Data from these trials will be presented at the American Society of Clinical Oncology (ASCO) annual meeting, which gets underway today in Chicago:
Erbitux, which competes with Genentech and Roche's Avastin, is licensed in Europe for previously-treated patients with mCRC and locally advanced squamous cell carcinoma of the head and neck (SCCHN). In the U.S. Erbitux is approved for colorectal and head and neck cancers in the U.S., where it is co-marketed by Bristol-Myers Squibb ( BMY - Get Report) and ImClone ( IMCL). Full data from the FLEX trial on Erbitux in advanced non-small cell lung cancer will also be presented at ASCO over the weekend. Bristol and ImClone were trading and up 1.2% and 0.9%, respectively. Competitor Genentech edged down 0.6%, to $70.50.