Highlights
Japan’s Takeda buys PvP Biologics in $330m deal
PvP Biologics has been acquired following the conclusion of Phase 1 proof-of-mechanism study of investigational medic
Novartis, DNDi to jointly develop LXE408 for visceral leishmaniasis
LXE408 was discovered at Novartis with the financial backing of the Wellcome Trust. According to Novartis, more than
AstraZeneca divests global rights to Movantik
Movantik is a peripherally acting mu-opioid receptor antagonist (PAMORA) indicated for the treatment of opioid-induce
Lysogene receives FDA fast track designation for LYS-SAF302 gene therapy in MPS IIIA
LYS-SAF302, a second-generation gene therapy, is designed to deliver a functional copy of the SGSH (N-sulfoglucosamin
Genentech, Bicycle Therapeutics sign immuno-oncology therapies deal
Under a strategic collaboration agreement, the companies will involve in the discovery, development and commercialisa
Takeda’s ALUNBRIG gets FDA priority review for expanded indication in NSCLC
As per the supplemental New Drug Application (sNDA), the Japanese pharma company is seeking approval of ALUNBRIG for
TrueProfile.io and RAKMHSU sign first UAE partnership to strengthen graduates’ care
TrueProfile.io® and Ras al Khaimah Medical and Health Sciences University (RAKMHSU) have signed the first pivotal p
Janssen gets FDA breakthrough therapy status for JNJ-6372 to treat metastatic NSCLC
The designation enables to use of JNJ-6372 to treat patients with metastatic NSCLC with epidermal growth factor recep
Kala’s dry eye disease candidate KPI-121 meets objective in STRIDE 3 trial
Planned to be branded as EYSUVIS (loteprednol etabonate ophthalmic suspension) 0.25%, KPI-121 showed statistically si
AbbVie receives marketing authorisation from EC to shorten MAVIRET duration for treatment-
MAVIRET was already indicated as an 8-week, pan-genotypic (GT1-6), once-daily regimen for treatment-naïve HCV pati
Mount Sinai and Harbour BioMed collaborate to advance novel biotherapies to treat cancer a
The collaboration will also utilize the H2L2 Harbour Mice® platform to generate monoclonal antibodies against the
Novartis gets FDA nod for Isturisa to treat Cushing’s disease
The FDA approval allows Isturisa to treat adults with Cushing’s disease who either cannot undergo pituitary gl