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From a clinical perspective, the approval also confirms that the new tablet formulation offers comparable efficacy and safety to previously approved oral semaglutide doses

Initial Results of a Phase 2 Study of Guadecitabine (SGI-110), a Novel Subcutaneous (sc) Hypomethylating Agent, for Patients with Previously Untreated Intermediate-2 or High Risk Myelodysplastic Syndromes (MDS) or Chronic Myelomonocytic Leukemia (CMML)

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PHARMACOKINETICS In a relative bioavailability study in 15 healthy adult male volunteers, CARNITOR Tablets were found to be bio-equivalent to CARNITOR Oral Solution