Table 1.

 Pharmacokinetics of Rifabutin in Individuals Without HIV

ReferenceStudy PopulationNo.Therapy DurationDose, mg, and FrequencyCmax, μg/mLAUC0-24, μg-h/mLHalf-life, h
Allen 1998 [10]Healthy volunteers1114 d
24 d
150 QD0.16 ± 0.03
0.21 ± 0.04
1.61 ± 0.43
1.94 ± 0.48
N/A
Benedetti 1990 [11]Healthy volunteers71 d
10 d
450 QD
450 QD
0.62
0.61
9.29
5.80
45 ± 6
58 ± 7
Ford 2008 [12]Healthy volunteers1513 d300 QD 0.31
(0.27–0.37)
6.11
(5.33–7.01)a
N/A
Ghannad 2019 [13]Healthy volunteers1410 d300 QD 0.54 4.22 N/A
Hamzeh 2003 [14]Healthy volunteers1714 d300 QD0.40 ± 0.143.37 ± 0.86N/A
Kraft 2004 [15]Healthy volunteers 10
14
10 d
10 d
300 QD
300 QD
0.29
0.29
2.56
2.87
N/A
La Porte 2009 [16]Healthy volunteers20Single dose 150 once0.16
(0.06–0.44)
2.22
(0.90–6.03)
41.3
(11.7–84.8)
Narang 1992 [17]Healthy volunteers15Single dose 150 once, fasted (solution)
150 once, with food (capsule)
150 once, fasted (capsule)
0.24
0.16
0.19
2.71b  
2.41b  
2.27b
N/A
Polk 2001 [18]Healthy male volunteers1114 d300 QD0.38
(0.30–0.48)
3.39
(2.84–4.03)
N/A
Sekar 2010 [19]Healthy volunteers1512 d300 QD0.57 ± 0.134.66 ± 0.97N/A
van Ingen 2012 [20]Pulmonary MAC51N/A4.80 ± 1.46 mg/kg 0.52 ± 0.292.28 ± 1.31cN/A
Zhang 2011 [21]Healthy volunteers11
9
20 d
20 d
150 QD
150 QD
0.19 ± 0.05
0.18 ± 0.06
1.80 ± 0.40
1.80 ± 0.40
N/A
Zhang 2011 [22]Healthy volunteers 14 10 d150 QD0.19 (30)1.85 (32)N/A
ReferenceStudy PopulationNo.Therapy DurationDose, mg, and FrequencyCmax, μg/mLAUC0-24, μg-h/mLHalf-life, h
Allen 1998 [10]Healthy volunteers1114 d
24 d
150 QD0.16 ± 0.03
0.21 ± 0.04
1.61 ± 0.43
1.94 ± 0.48
N/A
Benedetti 1990 [11]Healthy volunteers71 d
10 d
450 QD
450 QD
0.62
0.61
9.29
5.80
45 ± 6
58 ± 7
Ford 2008 [12]Healthy volunteers1513 d300 QD 0.31
(0.27–0.37)
6.11
(5.33–7.01)a
N/A
Ghannad 2019 [13]Healthy volunteers1410 d300 QD 0.54 4.22 N/A
Hamzeh 2003 [14]Healthy volunteers1714 d300 QD0.40 ± 0.143.37 ± 0.86N/A
Kraft 2004 [15]Healthy volunteers 10
14
10 d
10 d
300 QD
300 QD
0.29
0.29
2.56
2.87
N/A
La Porte 2009 [16]Healthy volunteers20Single dose 150 once0.16
(0.06–0.44)
2.22
(0.90–6.03)
41.3
(11.7–84.8)
Narang 1992 [17]Healthy volunteers15Single dose 150 once, fasted (solution)
150 once, with food (capsule)
150 once, fasted (capsule)
0.24
0.16
0.19
2.71b  
2.41b  
2.27b
N/A
Polk 2001 [18]Healthy male volunteers1114 d300 QD0.38
(0.30–0.48)
3.39
(2.84–4.03)
N/A
Sekar 2010 [19]Healthy volunteers1512 d300 QD0.57 ± 0.134.66 ± 0.97N/A
van Ingen 2012 [20]Pulmonary MAC51N/A4.80 ± 1.46 mg/kg 0.52 ± 0.292.28 ± 1.31cN/A
Zhang 2011 [21]Healthy volunteers11
9
20 d
20 d
150 QD
150 QD
0.19 ± 0.05
0.18 ± 0.06
1.80 ± 0.40
1.80 ± 0.40
N/A
Zhang 2011 [22]Healthy volunteers 14 10 d150 QD0.19 (30)1.85 (32)N/A

Abbreviations: AUC, area under the curve; Cmax, maximal concentration; QD, once daily; N/A, not reported in study.

aAUC0-48, area under drug-concentration time curve from time of dosing to 48 hours after dosing.

bAUC0-168, area under drug-concentration time curve from time of dosing to 168 hours after dosing.

cAUC0-6/7, area under drug-concentration time curve from time of dosing to 6 or 7 hours after dosing.

Table 1.

 Pharmacokinetics of Rifabutin in Individuals Without HIV

ReferenceStudy PopulationNo.Therapy DurationDose, mg, and FrequencyCmax, μg/mLAUC0-24, μg-h/mLHalf-life, h
Allen 1998 [10]Healthy volunteers1114 d
24 d
150 QD0.16 ± 0.03
0.21 ± 0.04
1.61 ± 0.43
1.94 ± 0.48
N/A
Benedetti 1990 [11]Healthy volunteers71 d
10 d
450 QD
450 QD
0.62
0.61
9.29
5.80
45 ± 6
58 ± 7
Ford 2008 [12]Healthy volunteers1513 d300 QD 0.31
(0.27–0.37)
6.11
(5.33–7.01)a
N/A
Ghannad 2019 [13]Healthy volunteers1410 d300 QD 0.54 4.22 N/A
Hamzeh 2003 [14]Healthy volunteers1714 d300 QD0.40 ± 0.143.37 ± 0.86N/A
Kraft 2004 [15]Healthy volunteers 10
14
10 d
10 d
300 QD
300 QD
0.29
0.29
2.56
2.87
N/A
La Porte 2009 [16]Healthy volunteers20Single dose 150 once0.16
(0.06–0.44)
2.22
(0.90–6.03)
41.3
(11.7–84.8)
Narang 1992 [17]Healthy volunteers15Single dose 150 once, fasted (solution)
150 once, with food (capsule)
150 once, fasted (capsule)
0.24
0.16
0.19
2.71b  
2.41b  
2.27b
N/A
Polk 2001 [18]Healthy male volunteers1114 d300 QD0.38
(0.30–0.48)
3.39
(2.84–4.03)
N/A
Sekar 2010 [19]Healthy volunteers1512 d300 QD0.57 ± 0.134.66 ± 0.97N/A
van Ingen 2012 [20]Pulmonary MAC51N/A4.80 ± 1.46 mg/kg 0.52 ± 0.292.28 ± 1.31cN/A
Zhang 2011 [21]Healthy volunteers11
9
20 d
20 d
150 QD
150 QD
0.19 ± 0.05
0.18 ± 0.06
1.80 ± 0.40
1.80 ± 0.40
N/A
Zhang 2011 [22]Healthy volunteers 14 10 d150 QD0.19 (30)1.85 (32)N/A
ReferenceStudy PopulationNo.Therapy DurationDose, mg, and FrequencyCmax, μg/mLAUC0-24, μg-h/mLHalf-life, h
Allen 1998 [10]Healthy volunteers1114 d
24 d
150 QD0.16 ± 0.03
0.21 ± 0.04
1.61 ± 0.43
1.94 ± 0.48
N/A
Benedetti 1990 [11]Healthy volunteers71 d
10 d
450 QD
450 QD
0.62
0.61
9.29
5.80
45 ± 6
58 ± 7
Ford 2008 [12]Healthy volunteers1513 d300 QD 0.31
(0.27–0.37)
6.11
(5.33–7.01)a
N/A
Ghannad 2019 [13]Healthy volunteers1410 d300 QD 0.54 4.22 N/A
Hamzeh 2003 [14]Healthy volunteers1714 d300 QD0.40 ± 0.143.37 ± 0.86N/A
Kraft 2004 [15]Healthy volunteers 10
14
10 d
10 d
300 QD
300 QD
0.29
0.29
2.56
2.87
N/A
La Porte 2009 [16]Healthy volunteers20Single dose 150 once0.16
(0.06–0.44)
2.22
(0.90–6.03)
41.3
(11.7–84.8)
Narang 1992 [17]Healthy volunteers15Single dose 150 once, fasted (solution)
150 once, with food (capsule)
150 once, fasted (capsule)
0.24
0.16
0.19
2.71b  
2.41b  
2.27b
N/A
Polk 2001 [18]Healthy male volunteers1114 d300 QD0.38
(0.30–0.48)
3.39
(2.84–4.03)
N/A
Sekar 2010 [19]Healthy volunteers1512 d300 QD0.57 ± 0.134.66 ± 0.97N/A
van Ingen 2012 [20]Pulmonary MAC51N/A4.80 ± 1.46 mg/kg 0.52 ± 0.292.28 ± 1.31cN/A
Zhang 2011 [21]Healthy volunteers11
9
20 d
20 d
150 QD
150 QD
0.19 ± 0.05
0.18 ± 0.06
1.80 ± 0.40
1.80 ± 0.40
N/A
Zhang 2011 [22]Healthy volunteers 14 10 d150 QD0.19 (30)1.85 (32)N/A

Abbreviations: AUC, area under the curve; Cmax, maximal concentration; QD, once daily; N/A, not reported in study.

aAUC0-48, area under drug-concentration time curve from time of dosing to 48 hours after dosing.

bAUC0-168, area under drug-concentration time curve from time of dosing to 168 hours after dosing.

cAUC0-6/7, area under drug-concentration time curve from time of dosing to 6 or 7 hours after dosing.

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