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. Author manuscript; available in PMC: 2013 Oct 23.
Published in final edited form as: Gene Ther. 2012 Apr 5;20(3):255–261. doi: 10.1038/gt.2012.31

Table 1.

Dose level and schedule of cyclophosphamide used in humans and the corresponding doses in mice and hamsters

Human
(mg kg −1)
Route Intensity Mouse
(mg kg −1)
Hamster
(mg kg −1)
3–5 Intravenous Twice weekly 37–62 22–37
10–15 Intravenous Every 7–10 days 123–185 74–111
40–50a Intravenous Over 2–5 days 492–615 296–370
1–5a Oral Daily 12–62 7–37
a

Human equivalent schedules used in this murine study. To convert human doses expressed in mg kg−1 to animal doses, the human dose was multiplied by a factor of 12.3 for mouse and 7.4 for hamster. Clinical dose schedules were obtained from the Thomson Reuters (Healthcare) (Greenwood Village, CO, USA) DRUGDEX database.19 Human-to-animal conversion factors are based on recommendation by the US Food and Drug Administration for estimating the maximum safe starting dose in clinical trials.20 Mice were dosed intraperitoneally at 120 mg kg−1 daily for 4 days (human 10 mg kg−1 × 4 doses) or by oral gavage at 40 mg kg−1 daily for 8 days (human 3 mg kg−1 × 8).