Safety assessment The tolerability and safety of the study medication were continuously monitored from baseline to endpoint in terms of study discontinuations and by comparing the treatment groups with respect to rates of AE, changes in laboratory test values, changes in vital signs, electrocardiogram abnormalities, and treatment-emergent physical findings
Both oral and subcutaneous injection are effective
J Pediatr Gastroenterol Nutr 7:220224 Minkler PE, Hoppel CL (1993) Quantification of carnitine and specific acylcarnitines by high-performance liquid chromatography: application to normal human urine and urine from patients with methylmalonic aciduria, isovaleric acidemia or medium-chain acyl-CoA dehydrogenase deficiency
Its Phase 2 obesity program did not meet the primary weight-loss endpoint, development was discontinued, and the compound is not FDA-approved or TGA-approved for any indication
doi: 10.1212/WNL.0b013e3181b9cebc
Curcumin and cancer
