Journal
REGULATORY TOXICOLOGY AND PHARMACOLOGY
Volume 67, Issue 1, Pages 89-97Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yrtph.2013.07.002
Keywords
Dapagliflozin; Occupational exposure limit; Pharmacokinetics; SGLT2 inhibitors; Urinary glucose excretion
Categories
Funding
- Bristol-Myers Squibb Co.
- AstraZeneca
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Classical risk assessment models for setting safe occupational exposure limits (OEL) have used multiple uncertainty factors (UF) applied to a point of departure (POD), e.g., a No Observed Effect Level (NOEL), which in some cases is the pharmacological effect. Dapagliflozin promotes glucosuria by inhibiting the renal sodium-glucose cotransporter-2 transporter. The initial OEL for dapagliflozin (0.002 mg/m(3)) was calculated when low dose clinical data was not available to identify a NOEL resulting in the need to use excessive UFs. To reduce the UFs from the OEL, a clinical pharmacodynamic [glucosuria and urinary glucose dipstick (UGD)] and pharmacokinetic study was conducted with single oral doses of 0.001, 0.01, 0.1, 0.3, 1.0 or 2.5 mg administered to 36 healthy subjects. Dose-related dapagliflozin systemic exposures were observed at doses >= 0.1 mg and glucosuria was observed at doses >= 0.3 mg and corroborated by UGD. The NOEL was therefore 0.1 mg for glucosuria. For setting the new OEL, no UFs were required. Dividing the POD by 10 m(3) (the volume of air an adult inhales in a workday), the resulting OEL was 0.01 mg/m(3). In conclusion, low-dose clinical pharmacodynamic and pharmacokinetic data can allow the OEL to be adjusted to the highest safe level. (C) 2013 Elsevier Inc. All rights reserved.
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