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5 The rule requires the submission of baseline or demographic characteristic measured in the clinical trial, including age, sex/gender, race, ethnicity (if collected under the protocol) for trials that are required to be registered under Section 11.22 (Phase 1 trials are excluded), 6 for reporting purposes via ClinicalTrials.gov

Drug approval package: Cymbalta (duloxetine hydrochloride), 20, 30, and 60 mg capsules

Most reported adverse events are local irritation or contact dermatitis, generally mild and self-limited

Sam37 is crucial for formation of the mitochondrial TOM-SAM supercomplex, thereby promoting -barrel biogenesis