US regulators have approved the first drug to treat neurotrophic keratitis, a rare degenerative disease affecting the cornea.
US regulators have approved the first drug to treat neurotrophic keratitis, a rare degenerative disease affecting the cornea.
Rare disease group Swedish Orphan Biovitrum (Sobi) says it has gained NHS England reimbursement for Ravicti for long-term management of urea-cycle disorders (UCDs) in adults and children.
Swiss biotech Novimmune has submitted a marketing application in Europe seeking permission to market its lead compound emapalumab for the treatment of patients with primary Hemophagocytic Lymphohistiocytosis (HLH).
AstraZeneca has announced mixed top-line results from the AERISTO Phase IIIb trial for Bevespi Aerosphere in patients with moderate to very severe chronic obstructive pulmonary disease (COPD).
Chippenham, UK-based Vectura says it has now successfully concluded two paediatric studies to support the potential use of asthma drug/device combo VR647.
A NICE green light is allowing men with benign prostatic hyperplasia to receive a procedure called transurethral water vapour ablation on the NHS.
MSD’s Keytruda has been awarded full approval in the US in combination with Lilly’s Alimta and platinum chemotherapy as first-line treatment for metastatic non-squamous non-small cell lung cancer.
A chemo/targeted drug combination being trialed by UK researchers has shown promise in patients with advanced ovarian or lung cancer in whom all other treatments have failed.
Cancer Research UK-funded scientists based at the University of Cambridge have identified a new target for the treatment of lung squamous cell carcinoma.
The World Health Organisation is calling on countries to implement broad measures to stop the spread of measles after the number of cases reached a record high in the region.
Pfizer’s lorlatinib has been designated a Promising Innovative Medicine for the treatment of some patients with ALK-positive advanced non-small cell lung cancer.
Novo Nordisk says trial data show an oral formulation of its GLP-1 analogue semaglutide provided superior HbA1c and weight reductions versus placebo in people with type II diabetes and renal impairment.
NHS trusts are warning that the health service is not prepared for a no-deal Brexit and that drug supplies could be affected as a result.
US regulators have further expanded the scope of Bristol Myers Squibb’s Opdivo, approving its use for a previously treated small cell lung cancer.
Cost regulators for the NHS in England and Wales have not approved funding for TiGenix and Takeda’s Alofisel – the first allogeneic stem cell therapy to be approved for use across the European Union – for use in Crohn’s patients in draft guidelines.