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- B34b29dcfc1c6b3cf89efbaed87a0a951 NCIT_P378 "CDISC" @default.
- B34b29dcfc1c6b3cf89efbaed87a0a951 type Axiom @default.
- B34b29dcfc1c6b3cf89efbaed87a0a951 annotatedProperty NCIT_P325 @default.
- B34b29dcfc1c6b3cf89efbaed87a0a951 annotatedSource NCIT_C165770 @default.
- B34b29dcfc1c6b3cf89efbaed87a0a951 annotatedTarget "A protocol designed for a parent study that provides the plan for coordinated conduct across the entirety of the study, with one or more substudies, which may have different objectives, to evaluate one or more investigational drugs and/or diseases within the overall trial structure. (FDA Guidance Document: Master Protocols: Efficient Clinical Trial Design Strategies to Expedite Development of Oncology Drugs and Biologics Guidance for Industry)" @default.