Literature DB >> 21701621

Incorrect description of mode of excretion of linagliptin.

Hans-Juergen Woerle1, Sanjay Patel.   

Abstract

Entities:  

Year:  2010        PMID: 21701621      PMCID: PMC3108713          DOI: 10.2147/dhps.s10440

Source DB:  PubMed          Journal:  Drug Healthc Patient Saf        ISSN: 1179-1365


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Dear Dr Zhou,

Boehringer Ingelheim, owner of the investigational drug linagliptin, would like to point out that in the recent review paper by Cox and colleagues,1 titled “Dipeptidyl peptidase-4 inhibitors in the management of type 2 diabetes: safety, tolerability, and efficacy”, which was published in Drug, Healthcare and Patient Safety, the authors have incorrectly described the mode of excretion for linagliptin as being predominantly renal. The correct statement should have read: “Excretion of linagliptin is predominantly nonrenal”, as described in the referenced pharmacokinetic study performed by Heise and colleagues.2 A nonrenal elimination route may be important in patients with renal impairment, which is common in patients with type 2 diabetes, so this distinction may be of clinical relevance. We would be grateful if you could clarify this for your readership to help avoid any confusion.
  2 in total

1.  Pharmacokinetics, pharmacodynamics and tolerability of multiple oral doses of linagliptin, a dipeptidyl peptidase-4 inhibitor in male type 2 diabetes patients.

Authors:  T Heise; E U Graefe-Mody; S Hüttner; A Ring; D Trommeshauser; K A Dugi
Journal:  Diabetes Obes Metab       Date:  2009-05-19       Impact factor: 6.577

2.  Dipeptidyl peptidase-4 inhibitors in the management of type 2 diabetes: safety, tolerability, and efficacy.

Authors:  Mary Elizabeth Cox; Jennifer Rowell; Leonor Corsino; Jennifer B Green
Journal:  Drug Healthc Patient Saf       Date:  2010-01-28
  2 in total

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