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R&D pipeline: where are we now and whats next Currently, GLP-1s have received regulatory approval from both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of: T2D

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These include: The type and dose of chemotherapy Previous radiation therapy Bone marrow involvement by cancer Pre-existing blood disorders Knowing these risk factors is key to early detection and management of CIT

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Whilst there is no medical evidence that one day offers superior clinical outcomes over another, practical considerations can influence your experience during the initial phase of treatment