Highlights
Seattle Genetics gets FDA priority review for tucatinib in locally advanced or metastatic
This NDA requests FDA approval of tucatinib in combination with trastuzumab and capecitabine for treatment of patient
The US FDA accepts for priority review Bristol-Myers Squibb’s BLA for liso-cel for
The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of August 17, 2020. “There remains a critica
Roche gets Chinese approval for Tecentriq plus chemotherapy to treat ES-SCLC
Tecentriq is a monoclonal antibody designed to bind with PD-L1 protein that is expressed on tumour cells and tumour-i
ALX Oncology announces closing of $105m Series C financing
Vivo Capital was the lead investor with other new investors including funds managed by Logos Capital, Janus Henderson
Deciphera Pharmaceuticals announces US FDA acceptance of NDA and priority review for ripre
The FDA granted Priority Review for the NDA, which provides for a six-month review, and assigned a Prescription Drug
Merck’s Keytruda plus chemotherapy meets primary endpoint in mTNBC trial
Keytruda plus chemotherapy achieved one of its dual primary endpoints of PFS in patients with mTNBC whose tumours exp
Cornerstone to Showcase AI-powered Innovations Disrupting HR at Learning Technologies UK 2
Cornerstone client Novartis will also be sharing how the company developed a culture of curiosity amongst its workforce
ASOS and Verint among 300 new customers for e-days as companies double down on absence man
Software provider sees customers like AXA move towards full integration of absence management software ASOS, Campari and
Harbour BioMed receives FDA IND approval for phase 2 trial and orphan drug designation for
Separately, the Agency’s Office of Orphan Products Development granted HBM9167 Orphan Drug Designation (ODD) f
Boehringer Ingelheim enters discovery stage collaboration with Trutino Biosciences
Under the terms of strategic alliance, Boehringer Ingelheim gains access to Trutino’s ODC platform technology
GSK, Innoviva seek EMA approval for Trelegy Ellipta to treat asthma in adults
The regulator has accepted the application for the use of once-daily and single-inhaler triple therapy, Trelegy Ellip
FDA advisory committee votes in favour of Lilly’s CYRAMZA as first-line treatment f
“Given the unmet need that remains in treating metastatic EGFR-mutated non-small cell lung cancer, we are encou