GSK’s blenrep combinations approved by UK MHRA in relapsed/refractory multiple myeloma
Blenrep combinations could redefine treatment as early as first relapse where more effective options are needed
Blenrep combinations could redefine treatment as early as first relapse where more effective options are needed
PCC has secured the commercialization rights for the EU, UK, and Norway and will be responsible for distributing Neoatricon in these regions
Bevqolva 25 mg/mL concentrate for infusion will be available in 4 mL (100 mg) and 16 mL (400 mg) single-use vials for infusion into veins
NULIBRY is a first-in-class synthetic cPMP substrate replacement therapy to reduce the risk of mortality in patients with MoCD Type A
The company had earlier announced about the approval received from the MHRA for Liraglutide
Yesafili, received marketing authorization approval from the European Commission for the European Union
This approval has come from the company's finished dosage form manufacturing facility
Company intends to increase sales in the UK to approximately 2 million Euros by focusing on seven molecules which are already registered in the country
With the combination of oral solid, inhalation, dermatology, high potent and oral contraceptive products, this is an important facility of the company
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