Otsuka’s Jinarc gets European marketing authorization to treat ADPKD
The drug is indicated for ADPKD patients who have chronic kidney disease (CKD) stage one to three at initiation of treatment with evidence of rapidly progressing disease. Tolvaptan
The European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) have granted paediatric clinical trial waivers to Shanton Pharma for its lead candidate SAP-001, easing the drug’s regulatory paths to approval.
Under the deal, the parties plan to pursue development and commercialization of Vibativ in hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia (HABP/VABP). The company said that additional indications
The Generex proprietary RapidMist drug delivery platform technology administers active pharmaceutical ingredient via aerosolized metered dose spray into the mouth for rapid absorption by the buccal mucosa. The
The companies have agreed to begin feasibility studies to evaluate how selected Novartis’ proprietary biologics can be delivered into the bloodstream using Rani’s unique route of administration. After
BPD is a field that includes cell engineering, continuous processing, formulation and analytical science, to support development of potential new therapies. The research collaboration will see MedImmune and