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Description
CD388 was given the Breakthrough Therapy designation by the FDA, and is currently being investigated in the Phase 3 ANCHOR study in adults and adolescents at high risk
While some CDMOs rely on rigid, standardised platforms to manage volume, this can limit their ability to accommodate the nuanced needs of different partners and products
2014, Scott et al
cAMP detection was using a Lance cAMP kit (PerkinElmer Life and Analytical Sciences), performed as previously described 6
Not the vague, hand-waving kind you find on most websites
Whatever happens, its important to remember that these drugs exist for a reason
