Highlights
Zealand’s dasiglucagon meets key endpoints in paediatric trial of severe hypoglycae
Invented and developed by Zealand Pharma, dasiglucagon is a potential first-in-class soluble glucagon analogue with a
Ipsen announces positive results from ENGAGE study of Dysport combo with GSC in adults wit
Results from the study will be presented at the MDS International Congress in Nice, France, September 22-26, 2019 as
Clovis Oncology acquires rights to FAP-targeted radiopharmaceutical programme from 3B Phar
The initial focus is on developing a peptide-targeted radionuclide therapy (PTRT) and imaging agent targeting fibrobl
FDA grants fast track status to Annexon’s ANX005 to treat Guillain-Barré Syndrom
GBS is a rare, acute and antibody-mediated autoimmune disease that will affect the peripheral nervous system. The dis
Themis begins phase 1 trial of MV-LASV Lassa fever vaccine candidate
The Austrian biotech company is partnering with the Coalition for Epidemic Preparedness Innovations (CEPI) for the de
Boehringer Ingelheim advances first pan-KRAS inhibitor BI 1701963 into clinical testing
Based on these results the compound has been advanced to Phase I clinical testing alone and in combination with trame
Femtogenix presents data on antibody drug conjugates containing reduced potency payloads i
The data is being presented at AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics,
FDA grants fast track status to Terns’s FXR agonist to treat NASH
NASH is a severe form of non-alcoholic fatty liver disease (NAFLD), which results due to the accumulation of excess f
GSK launches phase 3 programme for gepotidacin in uUTI and GC
The UK-based pharma company said that it has started dosing of patients in the phase 3 programme, which will test gep
EC approves Pfizer’s Bavencio plus axitinib to treat advanced RCC
Bavencio, which is a human anti-programmed death ligand-1 (PD-L1) antibody, has been demonstrated in preclinical mode
Gilead and Glympse Bio announce strategic collaboration for use of biomarker technology in
“We are excited about the opportunity to partner with Glympse Bio to help inform our NASH development program,
Imfinzi and Imfinzi plus tremelimumab delayed disease progression in POSEIDON trial
The trial met a primary endpoint by showing a statistically significant and clinically meaningful improvement in the