Trial Outcomes & Findings for Efficacy and Safety of AS012 in Subjects With Non-segmental Vitiligo (NCT NCT04487860)

NCT ID: NCT04487860

Last Updated: 2025-03-10

Results Overview

Vitiligo Area Scoring Index score: numeric score that can range from 0 to 100, with higher VASI scores denoting poorer the disease state

Recruitment status

COMPLETED

Study phase

PHASE2

Target enrollment

327 participants

Primary outcome timeframe

Week 24

Results posted on

2025-03-10

Participant Flow

Participant milestones

Participant milestones
Measure
Placebo
Part I: Up to 24 weeks: Subjects were randomized to Placebo Part II: week 24 to week 52: No Subjects Part III: week 52 to week 64: No Subjects
Placebo to AS012 Dose Regimen II at Week 24
Part I: Up to 24 weeks: No subjects Part II: week 24 to week 52: Subjects initially randomized to placebo were rerandomized to AS012 dose 2x Part III: week 52 to week 64: After week 52, the study treatment was stopped and all subjects entered the follow-up period to monitor safety and tolerability for 12 weeks after the last dose of study treatment.
Placebo to AS012 Dose Regimen IV at Week 24
Part I: Up to 24 weeks: No subjects Part II: week 24 to week 52: Subjects initially randomized to placebo were rerandomized to AS012 dose 6x Part III: week 52 to week 64: After week 52, the study treatment was stopped and all subjects entered the follow-up period to monitor safety and tolerability for 12 weeks after the last dose of study treatment.
AS012 Dose Regimen I
Part I: Up to 24 weeks: Subjects were randomized to AS012 dose x Part II: week 24 to week 52: Subjects originally randomized to AS012 doses remained on their assigned dosing regimen until the end of Part II (week 52). Part III: week 52 to week 64: After week 52,the study treatment was stopped and all subjects entered the follow-up period to monitor safety and tolerability for 12 weeks after the last dose of study treatment.
AS012 Dose Regimen II
Part I: Up to 24 weeks: Subjects were randomized to AS012 dose 2x Part II: week 24 to week 52: Subjects originally randomized to AS012 doses remained on their assigned dosing regimen until the end of Part II (week 52). Part III: week 52 to week 64: After week 52, the study treatment was stopped and all subjects entered the follow-up period to monitor safety and tolerability for 12 weeks after the last dose of study treatment.
AS012 Dose Regimen III
Part I: Up to 24 weeks: Subjects were randomized to AS012 dose 4x Part II: week 24 to week 52: Subjects originally randomized to AS012 doses remained on their assigned dosing regimen until the end of Part II (week 52). Part III: week 52 to week 64: After week 52, the study treatment was stopped and all subjects entered the follow-up period to monitor safety and tolerability for 12 weeks after the last dose of study treatment.
AS012 Dose Regimen IV
Part I: Up to 24 weeks: Subjects were randomized to AS012 dose 6x Part II: week 24 to week 52: Subjects originally randomized to AS012 doses remained on their assigned dosing regimen until the end of Part II (week 52). Part III: week 52 to week 64: After week 52 the study treatment was stopped and all subjects entered the follow-up period to monitor safety and tolerability for 12 weeks after the last dose of study treatment.
Part 1
STARTED
59
0
0
62
71
63
72
Part 1
COMPLETED
40
0
0
44
59
46
54
Part 1
NOT COMPLETED
19
0
0
18
12
17
18
Part 2
STARTED
0
20
20
44
59
46
54
Part 2
COMPLETED
0
12
14
28
36
34
38
Part 2
NOT COMPLETED
0
8
6
16
23
12
16
Part 3
STARTED
0
12
14
28
36
34
38
Part 3
COMPLETED
0
11
14
27
35
31
34
Part 3
NOT COMPLETED
0
1
0
1
1
3
4

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Placebo
n=59 Participants
Placebo
Placebo to AS012 Dose Regimen II at Week 24
n=20 Participants
Placebo to AS012 dose 2x at Week 24
Placebo to AS012 Dose Regimen IV at Week 24
n=20 Participants
Placebo to AS012 dose 6x at Week 24
AS012 Dose Regimen I
n=62 Participants
AS012 dose x
AS012 Dose Regimen II
n=71 Participants
AS012 dose 2x
AS012 Dose Regimen III
n=63 Participants
AS012 dose 4x
AS012 Dose Regimen IV
n=72 Participants
AS012 dose 6x
Total
n=367 Participants
Total of all reporting groups
Age, Continuous
Placebo and AS012 Regimens
44.2 years
STANDARD_DEVIATION 14.65 • n=59 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
48.1 years
STANDARD_DEVIATION 14.85 • n=62 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
45.2 years
STANDARD_DEVIATION 12.87 • n=71 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
46.8 years
STANDARD_DEVIATION 14.52 • n=63 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
41.8 years
STANDARD_DEVIATION 15.18 • n=72 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
45.1 years
STANDARD_DEVIATION 14.49 • n=327 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Age, Continuous
Placebo to AS012 Regimens
45.6 years
STANDARD_DEVIATION 14.81 • n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
43.3 years
STANDARD_DEVIATION 16.76 • n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
44.5 years
STANDARD_DEVIATION 15.66 • n=40 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Sex: Female, Male
Placebo and AS012 Regimens · Female
31 Participants
n=59 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
32 Participants
n=62 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
38 Participants
n=71 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
36 Participants
n=63 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
34 Participants
n=72 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
171 Participants
n=327 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Sex: Female, Male
Placebo and AS012 Regimens · Male
28 Participants
n=59 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
30 Participants
n=62 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
33 Participants
n=71 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
27 Participants
n=63 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
38 Participants
n=72 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
156 Participants
n=327 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Sex: Female, Male
Placebo to AS012 Regimens · Female
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
11 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
8 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
19 Participants
n=40 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Sex: Female, Male
Placebo to AS012 Regimens · Male
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
9 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
12 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
21 Participants
n=40 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Ethnicity (NIH/OMB)
Placebo and AS012 Regimens · Hispanic or Latino
19 Participants
n=59 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
18 Participants
n=62 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
17 Participants
n=71 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
15 Participants
n=63 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
16 Participants
n=72 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
85 Participants
n=327 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Ethnicity (NIH/OMB)
Placebo and AS012 Regimens · Not Hispanic or Latino
40 Participants
n=59 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
44 Participants
n=62 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
54 Participants
n=71 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
48 Participants
n=63 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
56 Participants
n=72 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
242 Participants
n=327 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Ethnicity (NIH/OMB)
Placebo and AS012 Regimens · Unknown or Not Reported
0 Participants
n=59 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=62 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=71 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=63 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=72 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=327 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Ethnicity (NIH/OMB)
Placebo to AS012 Regimens · Hispanic or Latino
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
8 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
6 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
14 Participants
n=40 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Ethnicity (NIH/OMB)
Placebo to AS012 Regimens · Not Hispanic or Latino
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
12 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
14 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
26 Participants
n=40 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
Ethnicity (NIH/OMB)
Placebo to AS012 Regimens · Unknown or Not Reported
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=20 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.
0 Participants
n=40 Participants • Subjects initially randomized to placebo were rerandomized to AS012 dose 2x or AS012 dose 6x in Part II of the study and therefore the data are reported separately for the "Placebo to AS012 Dose Regimen" arms.

PRIMARY outcome

Timeframe: Week 24

Vitiligo Area Scoring Index score: numeric score that can range from 0 to 100, with higher VASI scores denoting poorer the disease state

Outcome measures

Outcome measures
Measure
Placebo
n=59 Participants
Placebo
AS012 Dose Regimen I
n=62 Participants
AS012 dose x
AS012 Dose Regimen II
n=71 Participants
AS012 dose 2x
AS012 Dose Regimen III
n=63 Participants
AS012 dose 4x
AS012 Dose Regimen IV
n=72 Participants
AS012 dose 6x
AS012 Dose Regimen IV
AS012 dose 6x
Mean Change From Baseline in Vitiligo Area Scoring Index Score
-0.472 score on a scale
Standard Deviation 1.0422
-0.271 score on a scale
Standard Deviation 2.5139
-0.706 score on a scale
Standard Deviation 1.7301
-1.145 score on a scale
Standard Deviation 2.7721
-0.110 score on a scale
Standard Deviation 2.6168

SECONDARY outcome

Timeframe: Week 24

The Vitiligo Extent Score (VES) measures the overall vitiligo involvement in the body based on clinical pictures reflecting the natural distribution of the disease across 19 body areas (e.g., face, trunk, arms, legs, hands, axillae, back, gluteal). For each area, one representative image is selected, assigning one of six degrees of involvement (1%, 5%, 10%, 25%, 50%, 75%). The total and final score is the sum of the measurements from all areas, calculated using a conversion table available in the online calculator (www.vitiligo-calculator.com), and expressed as the extension of body surface area affected (0-100). Higher scores indicate worse clinical involvement. The VES change from baseline to Week 24 was assessed for the ITT population.

Outcome measures

Outcome measures
Measure
Placebo
n=59 Participants
Placebo
AS012 Dose Regimen I
n=62 Participants
AS012 dose x
AS012 Dose Regimen II
n=71 Participants
AS012 dose 2x
AS012 Dose Regimen III
n=63 Participants
AS012 dose 4x
AS012 Dose Regimen IV
n=72 Participants
AS012 dose 6x
AS012 Dose Regimen IV
AS012 dose 6x
Mean Change From Baseline in Vitiligo Extent Score (VES) on Clinical Pictures
-0.507 score on a scale
Standard Deviation 1.7427
-0.671 score on a scale
Standard Deviation 2.2065
-0.284 score on a scale
Standard Deviation 2.4793
-0.454 score on a scale
Standard Deviation 2.1214
-1.218 score on a scale
Standard Deviation 3.3963

SECONDARY outcome

Timeframe: Week 24

Subjects will be asked to complete a questionnaire to assess the burden experienced by individuals affected. For each of the statements in the Vitiligo Impact Patient Scale, 7 responses are suggested: always, very often, often, sometimes, rarely, never and not applicable. The individual answered as spontaneously as possible while thinking about their situation over the last 7 days. Summary scores range from 0 to 100. Higher values indicate a worse clinical condition.

Outcome measures

Outcome measures
Measure
Placebo
n=59 Participants
Placebo
AS012 Dose Regimen I
n=62 Participants
AS012 dose x
AS012 Dose Regimen II
n=71 Participants
AS012 dose 2x
AS012 Dose Regimen III
n=63 Participants
AS012 dose 4x
AS012 Dose Regimen IV
n=72 Participants
AS012 dose 6x
AS012 Dose Regimen IV
AS012 dose 6x
Mean Change in Vitiligo Impact Patient Scale
-2.72 score on a scale
Standard Deviation 12.575
-3.48 score on a scale
Standard Deviation 13.603
-4.24 score on a scale
Standard Deviation 18.984
-2.50 score on a scale
Standard Deviation 11.506
-2.06 score on a scale
Standard Deviation 15.082

SECONDARY outcome

Timeframe: Week 52

Description: The investigator will perform an average assessment of all vitiligo lesions. The following scale will be used for the PGA: Score 0= No involvement, Score 1= Limited, Score 2= moderate, Score 3= Extensive or Score 4= Very extensive. Higher values indicate a worse clinical condition. The static Physician's Global Assessment determines vitiligo extend at a single point in time, without taking the baseline disease condition into consideration, in other words, represents the Proportion of subjects achieving a PGA score of "no involvement" (score 0) or "limited extent" (score 1) with at least 2-point reduction from Baseline Week 52.

Outcome measures

Outcome measures
Measure
Placebo
n=12 Participants
Placebo
AS012 Dose Regimen I
n=14 Participants
AS012 dose x
AS012 Dose Regimen II
n=27 Participants
AS012 dose 2x
AS012 Dose Regimen III
n=36 Participants
AS012 dose 4x
AS012 Dose Regimen IV
n=34 Participants
AS012 dose 6x
AS012 Dose Regimen IV
n=38 Participants
AS012 dose 6x
Physician's Global Assessment Scores
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
0 Participants

SECONDARY outcome

Timeframe: Week 52

The DLQI scores are based on the response from the patient. Each question is scored from 0 (not affected at all) to 3 (very much affected). The DLQI is calculated by summing the score of each question resulting in a maximum of 30 and a minimum of 0. The higher the score, the more quality of life is impaired OR lower scores indicate better quality of life.

Outcome measures

Outcome measures
Measure
Placebo
n=12 Participants
Placebo
AS012 Dose Regimen I
n=14 Participants
AS012 dose x
AS012 Dose Regimen II
n=28 Participants
AS012 dose 2x
AS012 Dose Regimen III
n=36 Participants
AS012 dose 4x
AS012 Dose Regimen IV
n=34 Participants
AS012 dose 6x
AS012 Dose Regimen IV
n=38 Participants
AS012 dose 6x
Mean Change From Baseline in Dermatology Life Quality Index
0.2 score on a scale
Standard Deviation 2.12
0.0 score on a scale
Standard Deviation 3.33
-0.8 score on a scale
Standard Deviation 3.08
-0.6 score on a scale
Standard Deviation 4.76
-2.0 score on a scale
Standard Deviation 3.49
-0.2 score on a scale
Standard Deviation 2.51

Adverse Events

Placebo - Part I

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose Regimen I- Part I

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose Regimen II - Part I

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose Regimen III - Part I

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose Regimen IV - Part I

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Placebo to AS012 Dose Regimen II at Week 24 - Part II

Serious events: 0 serious events
Other events: 1 other events
Deaths: 0 deaths

Placebo to AS012 Dose Regimen IV at Week 24 - Part II

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose - Regimen I - Part II

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose Regimen II - Part II

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose Regimen III - Part II

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 Dose Regimen IV - Part II

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

AS012 - Part III

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Other adverse events
Measure
Placebo - Part I
n=59 participants at risk
Placebo - Part I
AS012 Dose Regimen I- Part I
n=62 participants at risk
AS012 dose x- Part I
AS012 Dose Regimen II - Part I
n=70 participants at risk
AS012 dose 2x- Part I
AS012 Dose Regimen III - Part I
n=63 participants at risk
AS012 dose 4x- Part I
AS012 Dose Regimen IV - Part I
n=72 participants at risk
AS012 dose 6x- Part I
Placebo to AS012 Dose Regimen II at Week 24 - Part II
n=20 participants at risk
Placebo to AS012 dose 2x at Week 24 - Part II
Placebo to AS012 Dose Regimen IV at Week 24 - Part II
n=20 participants at risk
Placebo to AS012 dose 6x at Week 24 - Part II
AS012 Dose - Regimen I - Part II
n=44 participants at risk
AS012 dose X- Part II
AS012 Dose Regimen II - Part II
n=59 participants at risk
AS012 dose 2 x - Part II
AS012 Dose Regimen III - Part II
n=46 participants at risk
AS012 dose 4 x - Part II
AS012 Dose Regimen IV - Part II
n=54 participants at risk
AS012 dose 6 x - Part II
AS012 - Part III
n=162 participants at risk
treatment free
Renal and urinary disorders
Haematuria
0.00%
0/59 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/62 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/70 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/63 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/72 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
5.0%
1/20 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/20 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/44 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/59 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/46 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/54 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received
0.00%
0/162 • 64 Week
The Safety Population will consist of all subjects who were randomized into the study and dispensed study drug. This population will be the primary population for the safety analysis. Subjects will be analyzed according to the actual treatment received

Additional Information

Dr. Fabio Ikedo

Aché Laboratórios Farmacêuticos S.A

Phone: 55 11 26086933

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place