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. Author manuscript; available in PMC: 2023 Aug 1.
Published in final edited form as: J Clin Pharmacol. 2022 Mar 2;62(8):960–969. doi: 10.1002/jcph.2034

Table 1.

Population demographics for metformin pediatric pharmacokinetic studies.

Non-overweight a Overweight / obesity b Severe obesity,
insulin resistant c
n 6 22 30
Dose (mg) 850, qd (n=5) 1,000, bid (n=19) 1,000, bid (n=28)
425, qd (n=1) 500, bid (n=3) 500, bid (n=2)
Formulation Immediate-release tablet Immediate-release tablet Immediate-release tablet d
PK study
 Prandial state Fed Fasted e Fasted e
 Steady state Yes Yes Yes
 Duration, h 12 8 12
Population Northern Spanish / Catalan (Barcelona, Spain) White ('s-Hertogenbosch, the Netherlands) 57% White, 40% African American, 3% Asian (United States); 10% Hispanic / Latino
Age, y 9.5 (9.3 – 9.9) 14 (11 – 18) 11 (7.7 – 14)
Weight, kg 33.3 (23.0 – 40.7) 79.3 (54.7 – 105) 77.0 (50.5 – 118)
Female, % 100 73 57
BMI, kg/m2 18.5 (15.7 – 21.0) 29.1 (22.9 – 39.3) 33.5 (24.2 – 43.6)
eGFR, mL/min/1.73 m2 -- 112 (94.1 – 136) f 129 (91.7 – 188) g

Data are expressed as mean (range) for continuous variables.

a

Clinical trial (isrctn.com ISRCTN49334271) in non-overweight girls with history of low birth weight and early-normal onset of puberty who were receiving 850 mg/day for 8 months; for the PK study, all girls received 850 mg metformin with dinner, except for 1 girl who accidentally received half that dose (425 mg).12

b

Clinical study (ClinicalTrials.gov NCT01487993) in 22 adolescents classified as either overweight or obese receiving 1,000 mg (or 500 mg for three subjects) of metformin twice daily for 37 weeks; blood samples for the PK study were collected during an oral glucose tolerance test.13

c

Six-month clinical trial (ClinicalTrials.gov NCT00005669) in children and adolescents with severe obesity receiving 1,000 mg (or 500 mg for two patients) of metformin; blood samples for the PK study were collected during a hyperglycemic clamp.14

d

Metformin capsules were manufactured and packaged by the National Institutes of Health Pharmaceutical Development Section.

e

Pharmacokinetic study was performed during a glucose tolerance test.

f

Published values were calculated using the Bedside Schwartz Equation

g

Published values were calculated using the CKiD Schwartz Equation.

bid, twice daily; BMI, body mass index; eGFR, estimated glomerular filtration rate; PK, pharmacokinetic; qd, once daily.