Civitas launches Phase 2a Clinical Study of CVT-301
CVT-301 provides immediate onset of a large and precise dose of L-dopa. The Phase 2a study is a randomized, placebo-controlled, single dose, cross-over design that will feature the
The US Food and Drug Administration (FDA) is set to review Kowa Pharmaceuticals America’s new drug application (NDA) for K-911, an investigational once-daily eye drop aimed at reducing intraocular pressure (IOP) in open-angle glaucoma (OAG) or ocular hypertension (OHT) patients.
Under the agreement Clarity’s PET based companion diagnostics and radio-immunotherapeutics development program will receive cGMP chemistry manufacturing,scale up and aseptic fill/finish services and analytical support from Dalton Pharma.