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Table 2 Subject disposition

From: Safety and efficacy of pyronaridine-artesunate in uncomplicated acute malaria: an integrated analysis of individual patient data from six randomized clinical trials

Subjects

PA safety

PA efficacy (ITT)

MQ + AS safety/efficacy

AL safety/efficacy

CQ safety

All comparators safetya

Treatedb

2815

2052

423

603

228

1254

Completed treatmentc

2773 (98.5)

2017 (98.3)

418 (98.8)

587 (97.3)

220 (96.5)

1225 (97.7)

Completed study

2410 (85.6)

1748 (85.2)

357 (84.4)

489 (81.1)

187 (82.0)

1033 (82.4)

Discontinued:

405 (14.4)

304 (14.8)

66 (15.6)

114 (18.9)

41 (18.0)

221 (17.6)

 Adverse event

46 (1.6)

32 (1.6)

4 (0.9)

10 (1.7)

2 (0.9)

16 (1.3)

 Consent withdrawn

26 (0.9)

19 (0.9)

6 (1.4)

11 (1.8)

5 (2.2)

22 (1.8)

 Insufficient therapeutic effect

11 (0.4)

0

0

0

0

0

 Lost to follow-up

99 (3.5)

69 (3.4)

25 (5.9)

10 (1.7)

12 (5.3)

47 (3.7)

 Protocol violation

9 (0.3)

4 (0.2)

0

1 (0.2)

0

1 (0.1)

 Malaria infection

186 (6.6)

174 (8.5)

29 (6.9)

78 (12.9)

21 (9.2)

128 (10.2)

 Other

28 (1.0)

6 (0.3)

2 (0.5)

4 (0.7)

1 (0.4)

7 (0.6)

  1. Data are n (%).
  2. PA, pyronaridine-artesunate; MQ + AS, mefloquine plus artesunate; AL, artemether-lumefantrine; CQ, chloroquine.
  3. a For comparators, MQ + AS, AL and CQ were included in the safety analysis; MQ + AS and AL in the efficacy analysis.
  4. b Received at least one dose of study medication.
  5. c Received all planned doses of study medication.