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FDA Greenlights Companion Diagnostic for Encorafenib Plus Cetuximab in BRAF V600E+ mCRC

The FDA has approved FoundationOne CDx for use as a companion diagnostic to determine patients with BRAF V600E–mutated metastatic colorectal cancer who may be candidates to receive encorafenib in combination with cetuximab.

Lilly erbituxFoundationone cdxEli lillyFoundationone liquidcdxFoundation medicine incDrug administrationAccessed junePrecision medicine in oncologyColorectal cancerBraf v600e mutated metastatic colorectal cancer

Erbitux Plus Encorafenib Approved for BRAF V600E Mutation-Positive Metastatic Colorectal Cancer

Erbitux Plus Encorafenib Approved for BRAF V600E Mutation-Positive Metastatic Colorectal Cancer
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David hymanEli lillyLilly erbituxDrug administrationAccessed september

SMC endorses Alexion s Ultomiris - PharmaTimes

SMC endorses Alexion’s Ultomiris 11th May 2021 The Scottish Medicines Consortium (SMC) has accepted a treatment for an ultra-rare disease that can cause progressive injury to vital organs via damage to the walls of blood vessels and blood clots in its May decisions. Restricted use of Alexion’s Ultomiris (ravulizumab) has been recommended by the SMC, for the treatment of patients with a body weight of 10kg or above with atypical haemolytic uremic syndrome (aHUS). Patients in Scotland who are complement inhibitor treatment-naïve or have previously received Alexion’s Soliris (eculizumab) for at least three months, and who have evidence of response to Soliris, are now eligible for the new treatment.

United kingdomAlexion ultomirisLen woodwardGlaxosmithkline zejulaAlexion solirisLilly erbituxScottish medicines consortiumRecordati rare diseasesஒன்றுபட்டது கிஂக்டம்லென் வூட்வார்ட்ஸ்காட்டிஷ் மருந்துகள் கூட்டமைப்பு