FDA OKs Roche’s Zelboraf for rare blood disease
US regulators have approved Roche’s Zelboraf (vemurafenib) for patients with a rare blood condition called Erdheim-Chester disease (ECD) carrying a mutation called BRAF V600
Read Moreby Selina McKee | Nov 8, 2017 | News | 0
US regulators have approved Roche’s Zelboraf (vemurafenib) for patients with a rare blood condition called Erdheim-Chester disease (ECD) carrying a mutation called BRAF V600
Read Moreby Selina McKee | Nov 7, 2016 | News | 0
Roche is planning to initiate late-stage studies investigating potential combinations for patients with advanced skin cancer based on its immunotherapy Tecentriq, which is already on the market for lung and bladder cancer.
Read Moreby Selina McKee | Oct 27, 2016 | News | 0
Cost regulators for treatments used by the NHS in England and Wales have published three sets of final guidances giving routine access to new options for lung cancer, rheumatoid arthritis and hepatitis C, and one rejecting a new therapy for melanoma.
Read Moreby Selina McKee | Sep 6, 2016 | News | 0
Patients in England and Wales with a certain type of advanced skin cancer will not be getting routine access to Roche’s Cotellic/Zelboraf combination on the NHS, after it was turned down by the National Institute for Health and Care Excellence.
Read Moreby Selina McKee | Jun 16, 2016 | News | 0
The National Institute for Health and Care Excellence is not backing National Health Service use of Roche’s Cotellic/Zelboraf as a treatment for melanoma.
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