Highlights
Sanofi, Translate Bio to develop novel mRNA vaccine for COVID-19 disease
The latest deal is said to leverage an existing agreement between the two companies established in 2018 for the devel
EMA grants orphan drug designation to AlloVir’s Viralym-M
Viralym-M is the company’s lead allogeneic, off-the-shelf, multi-virus specific T-cell therapy, being develope
FDA approves Bristol Myers Squibb’s ZEPOSIA oral treatment for relapsing forms of m
ZEPOSIA, an oral medication taken once daily, is the only approved sphingosine-1-phosphate (S1P) receptor modulator t
Novartis, life sciences firms collaborate with BMGF to fight against COVID-19 disease
Novartis, Boehringer Ingelheim, Bristol-Myers Squibb, Eisai, Eli Lilly, Gilead, GSK, Johnson & Johnson, Merck, Pf
ClinOne’s remote clinical trial patient management technology allows pharmaceutical
This need is especially acute in clinical trials as identified by the FDA. Trial sponsors, physicians and regulators
Infinity gets FDA fast track status for IPI-549, Opdivo combo in urothelial cancer
IPI-549 is an oral immuno-oncology candidate which has been designed to preferentially inhibit PI3K-gamma. The FDA fa
Alnylam Pharmaceuticals and Gen sign distribution agreement in Turkey for ONPATTRO (patisi
“Our partnership with Gen enables us to extend access to ONPATTRO to patients suffering from hereditary ATTR (h
Acceleron receives FDA breakthrough therapy designation for sotatercept in pulmonary arter
“In January of this year, we reported positive topline results from our PULSAR Phase 2 placebo-controlled trial
OncoImmune receives FDA approval for COVID-19 clinical trial
A cohort of 230 subjects with severe clinical symptoms will be randomized and administered a single dose of CD24Fc (4
FDA approves Pfizer’s Braftovi plus cetuximab to treat BRAFV600E-mutant metastatic
Braftovi, an oral small molecule kinase inhibitor, has been developed to target BRAF V600E. The approval was based on
Alnylam seeks FDA approval for lumasiran in primary hyperoxaluria type 1
In this connection, the RNAi therapeutics company completed the rolling submission of a new drug application (NDA) fo
CROMSOURCE announces launch of COVID-19 clinical trial
This trial is expected to be performed in Italy, though additional studies are planned by CROMSOURCE for other countr