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Table 2 Font trial: Clinical outcomes

From: Efficacy of galactose and adalimumab in patients with resistant focal segmental glomerulosclerosis: report of the font clinical trial group

Participant

Up/c month 0

Up/c month 6

% Change Up/c

Up/c responder

eGFR month 0

eGFR month 6

eGFR preservation

Primary outcome met?

Duration (yr) follow-up post randomization

RX = Adalimumab

1

2.1

12.3

475.0

No

325

41

No

No

2.5

2

6.3

6.6

5.0

No

140

155

Yes

No

2.0

3

14.9

8.4

−43.8

No

88

116

Yes

No

1.6

4

4.7

6.1

31.0

No

120

93

Yes

No

1.7

   5a,b

3.4

.

.

Never received study drug

81

.

Never received study drug

No

0.1

6

2.3

1.6

−30.5

No

37

29

Yes

No

1.5

7

2.1

5.2

142.5

No

58

24

No

No

1.7

RX = Galactose

8

9.0

3.2

−64.5

Yes

71

41

No

No

2.1

9

3.3

0.9

−72.8

Yes

143

129

Yes

Yes

1.7

10

3.3

0.5

−86.0

Yes

97

91

Yes

Yes

1.6

11

12.2

10.8

−11.4

No

91

63c

No

No

1.4

12a

49.3

29.9

−39.2

No

63

35

No

No

1.6

13

1.5

1.0

−29.9

No

221

180

Yes

No

1.3

14

6.7

7.0

4.7

No

71

67

Yes

No

1.1

RX = Standard Therapy (lisinopril, losartan, atorvastatin)

15

4.6

2.8

−40.3

No

276

283

Yes

No

2.1

16

16.0

5.0

−68.5

Yes

235

180

Yes

Yes

1.5

17a,b

11.6

.

.

Never received study drug

170

.

Never received study drug

No

0.0

18

3.2

2.5

−22.7

No

151

108

Yes

No

1.2

19

4.9

2.2

−54.6

Yes

155

150c

Yes

Yes

1.2

20

9.6

5.5

−42.2

No

173

178

Yes

No

1.7

21

11.5

14.2

23.2

No

94

.57c

No

No

1.8

  1. Abbreviations: eGFR, estimated glomerular filtration rate; Up/C urine protein:creatinine ratio 1) Excludes the subject randomized to Rosiglitazone; 2) One participant in each arm was neither on ACEi, nor ARB a,Participant did not receive neither ACEi, nor ARB; b, Participant did not start assigned trial therapy; cParticipant had eGFR calculated based on testing performed at a local laboratory