Highlights
Roche’s risdiplam achieves primary endpoint in infant-related spinal muscular atrop
The company has reported positive topline results from the pivotal part 2 of the FIREFISH study, which is assessing r
FDA approves TEPEZZA for the treatment of thyroid eye disease
TEPEZZA is the first and only FDA-approved medicine for the treatment of TED, a serious, progressive and vision-threa
Calidi Biotherapeutics secures series A investments to advance manufacturing
The investment efforts were led by Heehyoung Lee, Ph.D., co-founder and managing partner of LumeBio, advisor to Calid
Eli Lilly to build $470m pharmaceutical manufacturing facility in North Carolina
North Carolina Governor Roy Cooper has also announced that Eli Lilly’s move will also help to create over 460
US reports first case of novel coronavirus from China-returned traveller
The patient had travelled from Wuhan to Washington. The novel coronavirus infection is believed to have originated at
Novartis’ Mayzent gets EC nod for secondary progressive multiple sclerosis
The approval for Mayzent from the European Commission (EC) is for SPMS with active disease, confirmed by relapses or
Armas Pharmaceuticals adds four generic injectables as first launches of 2020
Armas Pharmaceuticals Inc. (Armas), has begun the new year with launches of four generic injectables: Caffeine Citrat
A2Dominion, BMJ, Carnival, Harrods, John Lewis, Nestle, Pladis, Sanofi Pasteur, The Adecco
The victorious were announced at a Gala ceremony at Troxy in London last night London – January 24, 2020 – T
Opdivo delivers superior five-year survival results in renal cell carcinoma
The company said that 26% of patients with previously treated advanced or metastatic renal cell carcinoma are alive a
Celltrion showcases positive one-year results for subcutaneous formulation of infliximab i
Results presented at The European Crohn’s and Colitis Organisation (ECCO) 2020 annual congress in Vienna, Austr
New phase 3b interim data from STARDUST study show majority patients with moderately to se
Intestinal ultrasound (IUS) responses were assessed and were detected as early as week 4.2 Week 16 data (digital oral
Epizyme seeks FDA accelerated approval for Tazverik to treat follicular lymphoma
The regulator has accepted the firm’s new drug application (NDA) for the accelerated approval of tazemetostat