List view / Grid view
23 December 2015 | By Victoria White
According to GlobalData, this rise will be driven by a number of factors, including an increased use of expensive biologics, and off-label use of therapies to treat the disease...
23 December 2015 | By Victoria White
Uptravi (selexipag) acts by relaxing muscles in the walls of blood vessels to dilate (open) blood vessels and decrease the elevated pressure in the vessels supplying blood to the lungs...
23 December 2015 | By Victoria White
The FDA has approved AstraZeneca’s Zurampic (lesinurad) in combination with xanthine oxidase inhibitor for the treatment of hyperuricemia associated with gout...
Dengvaxia is the first vaccine licensed for the prevention of dengue in the world...
23 December 2015 | By Victoria White
These new guidelines describe the important features of this disease and provide comprehensive treatment recommendations...
22 December 2015 | By Victoria White
The facility will produce ingredients manufactured using cell cultures and will create more than 400 new jobs in the Austrian capital...
22 December 2015 | By
Merck KGaA and Pfizer have announced the opening of trial sites for an international Phase III study of avelumab in patients with ovarian cancer...
22 December 2015 | By Victoria White
The PPRS is a unique scheme where pharmaceutical companies agreed to contribute towards the cost of medicines, with the aim of making the latest treatments affordable for the NHS...
22 December 2015 | By Victoria White
Enadenotucirev is an oncolytic virus that has been shown in Phase I clinical trials to reach and selectively infect cancer cells when administered by intravenous infusion...
21 December 2015 | By Victoria White
The study enrolled 73 previously-treated patients with severe haemophilia A younger than 12 years of age and assessed the treatment's haemostatic efficacy in prophylaxis and treatment of bleeding episodes...
21 December 2015 | By Victoria White
MSD has announced results from the Phase 2/3 KEYNOTE-010 study of Keytruda (pembrolizumab) in patients with previously treated non-small cell lung cancer (NSCLC)...
21 December 2015 | By Victoria White
BI 1482694 is Boehringer Ingelheim’s 3rd-generation, epidermal growth factor receptor mutation-specific tyrosine kinase inhibitor...
21 December 2015 | By Victoria White
The FDA has authorised Celyad’s IND application to proceed, thus allowing for the clinical testing of C-Cure cardiopioetic cells delivered via C-Cathez in a Phase III heart failure trial...
18 December 2015 | By Victoria White
The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion, recommending the marketing authorisation of AstraZeneca’s Tagrisso (AZD9291, osimertinib) 80mg once-daily tablets for the treatment of adult patients with locally advanced or metastatic epidermal growth factor receptor (EGFR) T790M mutation-positive non-small…
18 December 2015 | By Victoria White
Explaining his reasoning behind the company name change, Stanley Crooke, CEO of Ionis, told Forbes: “My underlying concern was that the name was a distraction"...
