News

Eisai, NHS and NICE fail to reach deal on Lenvima

Eisai, NHS and NICE fail to reach deal on Lenvima

Patients with an advanced form thyroid cancer may have to wait three years for NHS access to Eiasai’s Lenvima in England, after the drug was left out of the newly launched Cancer Drugs Fund.

Wales endorses NHS use of Celgene’s Revlimid

Wales endorses NHS use of Celgene’s Revlimid

Around 300 patients with multiple myeloma in Wales will get National Health Service access to treatment with Celgene’s Revlimid after the drug was recommended for first-line use by cost regulators.

US fast track for Shire’s liver drug

US fast track for Shire’s liver drug

US regulators have placed Shire’s SHP626 on a fast-track regulatory pathway in the hope of potentially accelerating access to the experimental liver disease drug.

EU nod for MSD hep C therapy

EU nod for MSD hep C therapy

European regulators have waved through Merck, Sharp & Dohme’s Zepatier bringing a new treatment option to patients with hepatitis C.

Controversial CDF revamp launches

Controversial CDF revamp launches

England’s Cancer Drugs Fund (CDF) reopens under its new model, but the industry is warning that it could do little to solve fundamental problems with drug reimbursement.

GSK bolsters asthma pipeline

GSK bolsters asthma pipeline

GSK has in-licensed a targeted biological therapy for severe asthma from Janssen, strengthening its respiratory pipeline.

GSK invests £275m in UK manufacturing

GSK invests £275m in UK manufacturing

GSK has announced that it will invest £275 million into three of its manufacturing sites in the UK to boost production and support delivery of its respiratory and large molecule biological drugs.