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Table 3 Sites of clinically suspected infections and use of antibiotics at baseline (safety population)

From: A placebo-controlled, double-blind, dose-escalation study to assess the safety, tolerability and pharmacokinetics/pharmacodynamics of single and multiple intravenous infusions of AZD9773 in patients with severe sepsis and septic shock

 

AZD9773 cohort 1

(50 U/kg)

(n= 8)

AZD9773 cohort 2

(250 U/kg)

(n= 9)

AZD9773 cohort 3

(250/50 U/kg) (n= 12)

AZD9773 cohort 4

(500/100 U/kg) (n= 10)

AZD9773 cohort 5

(750/250 U/kg)

(n= 8)

Placebo (n= 23)

Total

(n= 70)

Infection site, n (%)

   Abdomen

2 (25.0)

3 (33.3)

2 (16.7)

1 (10.0)

5 (62.5)

3 (13.0)

16 (22.9)

   Catheter/device

1 (12.5)

0

0

0

0

0

1 (1.4)

   Lung

3 (37.5)

4 (44.4)

6 (50.0)

6 (60.0)

2 (25.0)

12 (52.2)

33 (47.1)

   Skin and soft tissue

1 (12.5)

1 (11.1)

1 (8.3)

1 (10.0)

0

4 (17.4)

8 (11.4)

   Unknown

1 (12.5)

1 (11.1)

2 (16.7)

2 (20.0)

0

1 (4.3)

7 (10.0)

   Urinary tract

0

0

3 (25.0)

0

1 (12.5)

3 (13.0)

7 (10.0)

Time from qualifying organ failure to first antibiotic use, hours*

 

( n = 7)

( n = 6)

( n = 9)

( n = 7)

( n = 8)

( n = 19)

( n = 56)

Median

(range)

-4.4

(-39.0 to 20.6)

-10.1

(-85.7 to 0.7)

-0.8

(-41.3 to 16.4)

-3.9

(-108.2 to 1.2)

-6.3

(-85.1 to 6.5)

-4.9

(-366.5 to 12.8)

-4.2

(-366.5 to 20.6)

  1. *A negative time indicates that antibiotics were given before qualifying organ failure