A Study of Nivolumab by Itself or Nivolumab Combined With Ipilimumab in Patients With Advanced or Metastatic Solid Tumors
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT01928394 |
Recruitment Status :
Active, not recruiting
First Posted : August 23, 2013
Results First Posted : March 24, 2020
Last Update Posted : March 21, 2023
|
Sponsor:
Bristol-Myers Squibb
Information provided by (Responsible Party):
Bristol-Myers Squibb
- Study Details
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- Study Results
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Study Type | Interventional |
---|---|
Study Design | Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: None (Open Label); Primary Purpose: Treatment |
Condition |
Advanced or Metastatic Solid Tumors |
Interventions |
Biological: Nivolumab Biological: Ipilimumab Drug: Cobimetinib |
Enrollment | 1163 |
Participant Flow
Recruitment Details | |
Pre-assignment Details | 1131 participants were treated in total for TNBC, GC, PC, SCLC, BC and OC. |
Arm/Group Title | TNBC Arm N | TNBC Arm N-I Dose Level 1 | TNBC Arm N-I Dose Level 2 | GC Arm N | GC Arm N-I Dose Level 1 | GC Arm N-I Dose Level 2 | GC Arm N-I Dose Level 2b | PC Arm N | PC Arm N-I Dose Level 1 | PC Arm N-I Dose Level 2 | PC Arm N-I Dose Level 2d | SCLC Arm N - Pre-expansion | SCLC Arm N-I Dose Level 2 - Pre-expansion | SCLC Arm N Expansion | SCLC Arm N-I Dose Level 2- Expansion | SCLC Arm N-I Dose Level 1 - | SCLC Arm N-I Dose Level 2b | BC Arm N | BC Arm N-I Dose Level 2 | BC Arm N-I Dose Level 2b | OC Arm N-I Dose Level 2 | OC Arm N-I Dose Level 2b | OC Arm N-I Dose Level 2c: |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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Triple Negative Breast Cancer (TNBC) Nivolumab monotherapy (3 mg/kg) Q2W | Triple Negative Breast Cancer (TNBC) Nivolumab (1 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Triple Negative Breast Cancer (TNBC) Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Gastric Cancer (GC) Nivolumab 3 mg/kg Q2W | Gastric Cancer(GC) Nivolumab (1 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Gastric Cancer (GC) nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses; then nivolumab 3 mg/kg Q2W | Gastric Cancer (GC) Nivolumab 3 mg/kg + Ipilimumab 1 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Pancreatic cancer (PC) participants: Nivolumab 3 mg/kg Q2W | Pancreatic cancer (PC) participants: Nivolumab 1 mg/kg + Ipilimumab 1 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Pancreatic cancer (PC) participants: Nivolumab 1 mg/kg + Ipilimumab 3 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Pancreatic cancer (PC) participants: Nivolumab 3 mg/kg + Ipilimumab 1 mg/kg Q6W for 4 doses + cobimetinib 60 mg po qd 21 days on/7 days off | Small cell lung cancer (SCLC) participants treated in Pre-expansion Cohort with Nivolumab 3 mg/kg Q2W | Small cell lung cancer (SCLC) treated participants in Pre-expansion cohort treated with Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Small cell lung cancer (SCLC) expansion cohort participants: Nivolumab monotherapy (3 mg/kg) Q2W | Small cell lung cancer (SCLC) expansion cohort participants Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Small cell lung cancer (SCLC) participants treated with Nivolumab (1 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3mg/kg) Q2W | Small cell lung cancer (SCLC) treated participants treated with Nivolumab (3 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Bladder cancer (BC) participants: Nivolumab 3 mg/kg Q2W | Bladder cancer (BC) participants: Nivolumab 1 mg/kg + Ipilimumab 3 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Bladder cancer (BC) participants: Nivolumab 3 mg/kg + Ipilimumab 1 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W |
Ovarian cancer (OC) participants: Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W |
Ovarian cancer (OC) participants: Nivolumab (3 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses,then nivolumab (3 mg/kg) Q2W | Ovarian cancer (OC) participants: Nivolumab (3 mg/kg) Q2W + ipilimumab (1 mg/kg) Q6W |
Period Title: Treatment Period | |||||||||||||||||||||||
Started [1] | 18 | 3 | 18 | 59 | 3 | 49 | 52 | 18 | 3 | 18 | 30 | 98 | 61 | 147 | 96 | 3 | 55 | 78 | 92 | 104 | 41 | 43 | 42 |
Transition [2] | 3 | 0 | 0 | 9 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 17 | 0 | 2 | 0 | 0 | 0 | 20 | 0 | 0 | 0 | 0 | 0 |
Transition- Continued [3] | 0 | 0 | 3 | 0 | 0 | 3 | 6 | 0 | 1 | 1 | 0 | 0 | 17 | 0 | 2 | 0 | 0 | 0 | 1 | 19 | 0 | 0 | 0 |
Completed [4] | 0 | 0 | 0 | 3 | 0 | 6 | 3 | 0 | 0 | 0 | 0 | 5 | 6 | 8 | 8 | 1 | 5 | 7 | 22 | 8 | 1 | 1 | 3 |
Not Completed | 18 | 3 | 18 | 56 | 3 | 43 | 49 | 18 | 3 | 18 | 30 | 93 | 55 | 139 | 88 | 2 | 50 | 71 | 70 | 96 | 40 | 42 | 39 |
Reason Not Completed | |||||||||||||||||||||||
Disease progression | 17 | 2 | 12 | 48 | 3 | 25 | 38 | 16 | 3 | 11 | 22 | 73 | 38 | 118 | 59 | 1 | 43 | 56 | 50 | 71 | 30 | 31 | 31 |
Study drug toxicity | 1 | 1 | 3 | 3 | 0 | 9 | 7 | 1 | 0 | 5 | 2 | 3 | 7 | 5 | 12 | 0 | 3 | 3 | 12 | 15 | 4 | 7 | 4 |
AE unrelated to study drug | 0 | 0 | 2 | 3 | 0 | 5 | 1 | 0 | 0 | 2 | 0 | 12 | 6 | 13 | 6 | 1 | 1 | 6 | 3 | 5 | 1 | 1 | 0 |
Participant request to stop therapy | 0 | 0 | 0 | 0 | 0 | 3 | 3 | 0 | 0 | 0 | 3 | 2 | 1 | 2 | 4 | 0 | 1 | 3 | 1 | 1 | 3 | 1 | 3 |
Participant withdrew consent | 0 | 0 | 1 | 1 | 0 | 1 | 0 | 1 | 0 | 0 | 1 | 1 | 1 | 0 | 2 | 0 | 2 | 1 | 1 | 1 | 0 | 2 | 0 |
Poor/non-compliance | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 0 | 0 | 1 | 0 | 1 | 0 | 0 | 0 |
other reason | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 0 | 1 | 0 | 0 | 0 | 2 | 2 | 0 | 0 | 0 |
Maximum clinical benefit | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | 1 | 0 | 2 | 0 | 0 |
Lost to Follow-up | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
Death | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
[1]
Started = Entering initial treatment or combination treatment after completion of monotherapy(MT)
[2]
Participants who will transition after completing MT due to disease progression (DP)
[3]
Participants who were transitioned to another treatment after disease progression (DP).
[4]
Completed = continuing treatment period
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Period Title: Follow-up Period | |||||||||||||||||||||||
Started [1] | 15 | 3 | 18 | 50 | 3 | 49 | 52 | 16 | 3 | 18 | 30 | 81 | 61 | 145 | 96 | 3 | 55 | 58 | 92 | 104 | 41 | 43 | 42 |
Completed [2] | 12 | 3 | 15 | 40 | 3 | 41 | 40 | 10 | 2 | 16 | 19 | 59 | 47 | 107 | 66 | 3 | 41 | 50 | 76 | 83 | 32 | 34 | 36 |
Not Completed | 3 | 0 | 3 | 10 | 0 | 8 | 12 | 6 | 1 | 2 | 11 | 22 | 14 | 38 | 30 | 0 | 14 | 8 | 16 | 21 | 9 | 9 | 6 |
Reason Not Completed | |||||||||||||||||||||||
Participant withdrew consent | 3 | 0 | 1 | 4 | 0 | 2 | 5 | 1 | 0 | 0 | 5 | 8 | 2 | 12 | 7 | 0 | 5 | 3 | 2 | 7 | 4 | 6 | 2 |
Death | 0 | 0 | 2 | 6 | 0 | 6 | 6 | 2 | 1 | 2 | 4 | 12 | 11 | 25 | 18 | 0 | 6 | 5 | 13 | 13 | 5 | 3 | 2 |
other reason | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 3 | 0 | 0 | 2 | 1 | 0 | 1 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | 0 | 1 |
Lost to Follow-up | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 1 |
[1]
started = number of Participants regardless of continuing treatment or not.
[2]
completed = continuing to be followed
|
Baseline Characteristics
Arm/Group Title | TNBC Arm N | TNBC Arm N-I Dose Level 1 | TNBC Arm N-I Dose Level 2 | GC Arm N | GC Arm N-I Dose Level 1 | GC Arm N-I Dose Level 2 | GC Arm N-I Dose Level 2b | PC Arm N | PC Arm N-I Dose Level 1 | PC Arm N-I Dose Level 2 | PC Arm N-I Dose Level 2d | SCLC Arm N - Pre-expansion | SCLC Arm N-I Dose Level 2 - Pre-expansion | SCLC Arm N Expansion | SCLC Arm N-I Dose Level 2- Expansion | SCLC Arm N-I Dose Level 1 - | SCLC Arm N-I Dose Level 2b | BC Arm N | BC Arm N-I Dose Level 2 | BC Arm N-I Dose Level 2b | OC Arm N-I Dose Level 2 | OC Arm N-I Dose Level 2b: | OC Arm N-I Dose Level 2c: | Total | |
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Triple Negative Breast Cancer (TNBC) Nivolumab monotherapy (3 mg/kg) Q2W | Triple Negative Breast Cancer (TNBC) Nivolumab (1 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Triple Negative Breast Cancer (TNBC) Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Gastric Cancer (GC) Nivolumab 3 mg/kg Q2W | Gastric Cancer(GC) Nivolumab (1 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Gastric Cancer (GC) nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses; then nivolumab 3 mg/kg Q2W | Gastric Cancer (GC) Nivolumab 3 mg/kg + Ipilimumab 1 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Pancreatic cancer (PC) participants: Nivolumab 3 mg/kg Q2W | Pancreatic cancer (PC) participants: Nivolumab 1 mg/kg + Ipilimumab 1 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Pancreatic cancer (PC) participants: Nivolumab 1 mg/kg + Ipilimumab 3 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Pancreatic cancer (PC) participants: Nivolumab 3 mg/kg + Ipilimumab 1 mg/kg Q6W for 4 doses + cobimetinib 60 mg po qd 21 days on/7 days off | Small cell lung cancer (SCLC) participants treated in Pre-expansion Cohort with Nivolumab 3 mg/kg Q2W | Small cell lung cancer (SCLC) treated participants in Pre-expansion cohort treated with Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Small cell lung cancer (SCLC) expansion cohort participants:Nivolumab monotherapy (3 mg/kg) Q2W | Small cell lung cancer (SCLC) expansion cohort participants Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2Wi | Small cell lung cancer (SCLC) participants treated with Nivolumab (1 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3mg/kg) Q2W | Small cell lung cancer (SCLC) treated participants treated with Nivolumab (3 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W | Bladder cancer (BC) participants: Nivolumab 3 mg/kg Q2W | Bladder cancer (BC) participants: Nivolumab 1 mg/kg + Ipilimumab 3 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W | Bladder cancer (BC) participants: Nivolumab 3 mg/kg + Ipilimumab 1 mg/kg Q3W for 4 doses, then Nivolumab (3 mg/kg) Q2W |
Ovarian cancer (OC) participants: Nivolumab (1 mg/kg) + ipilimumab (3 mg/kg) Q3W for 4 doses, then nivolumab (3 mg/kg) Q2W |
Ovarian cancer (OC) participants: Nivolumab (3 mg/kg) + ipilimumab (1 mg/kg) Q3W for 4 doses,then nivolumab (3 mg/kg) Q2W | Ovarian cancer (OC) participants: Nivolumab (3 mg/kg) Q2W + ipilimumab (1 mg/kg) Q6W | Total of all reporting groups | |
Overall Number of Baseline Participants | 18 | 3 | 18 | 59 | 3 | 49 | 52 | 18 | 3 | 18 | 30 | 98 | 61 | 147 | 96 | 3 | 55 | 78 | 92 | 104 | 41 | 43 | 42 | 1131 | |
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[Not Specified]
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Age, Continuous
[1] Mean (Standard Deviation) Unit of measure: Years |
|||||||||||||||||||||||||
Number Analyzed | 18 participants | 3 participants | 18 participants | 59 participants | 3 participants | 49 participants | 52 participants | 18 participants | 3 participants | 18 participants | 30 participants | 98 participants | 61 participants | 147 participants | 96 participants | 3 participants | 55 participants | 78 participants | 92 participants | 104 participants | 41 participants | 43 participants | 42 participants | 1131 participants | |
53.3 (11.9) | 52.7 (9.5) | 49.1 (9.0) | 57.2 (10.99) | 67.0 (9.54) | 53.2 (12.58) | 56.4 (13.40) | 63.2 (9.70) | 58.3 (9.87) | 64.1 (9.21) | 62.1 (11.51) | 62.6 (8.50) | 63.9 (9.94) | 62.8 (9.09) | 63.7 (9.06) | 59.3 (6.7) | 60.1 (7.74) | 64.1 (10.86) | 63.9 (9.54) | 64.1 (9.69) | 56.7 (11.1) | 59.6 (10.9) | 58.7 (12.2) | 61.2 (10.7) | ||
[1]
Measure Analysis Population Description: All Treated Participants
|
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Age, Customized
[1] [2] Measure Type: Number Unit of measure: Participants |
Number Analyzed | 18 participants | 3 participants | 18 participants | 59 participants | 3 participants | 49 participants | 52 participants | 18 participants | 3 participants | 18 participants | 30 participants | 98 participants | 61 participants | 147 participants | 96 participants | 3 participants | 55 participants | 78 participants | 92 participants | 104 participants | 41 participants | 43 participants | 42 participants | 1131 participants |
< 65 | 16 | 3 | 18 | 42 | 1 | 39 | 35 | 5 | 2 | 9 | 13 | 55 | 27 | 82 | 47 | 2 | 38 | 37 | 47 | 57 | 30 | 26 | 25 | 656 | |
>= 65 and < 75 | 1 | 0 | 0 | 15 | 1 | 8 | 12 | 12 | 1 | 7 | 14 | 34 | 27 | 51 | 39 | 1 | 17 | 31 | 34 | 29 | 10 | 14 | 12 | 370 | |
>= 75 | 1 | 0 | 0 | 2 | 1 | 2 | 5 | 1 | 0 | 2 | 3 | 9 | 7 | 14 | 10 | 0 | 0 | 10 | 11 | 18 | 1 | 3 | 5 | 105 | |
>= 65 | 2 | 0 | 0 | 17 | 2 | 10 | 17 | 13 | 1 | 9 | 17 | 43 | 34 | 65 | 49 | 1 | 17 | 41 | 45 | 47 | 11 | 17 | 17 | 475 | |
[1]
Measure Description: Age categorization
[2]
Measure Analysis Population Description: All Treated Participants
|
|||||||||||||||||||||||||
Sex: Female, Male
[1] Measure Type: Count of Participants Unit of measure: Participants |
|||||||||||||||||||||||||
Number Analyzed | 18 participants | 3 participants | 18 participants | 59 participants | 3 participants | 49 participants | 52 participants | 18 participants | 3 participants | 18 participants | 30 participants | 98 participants | 61 participants | 147 participants | 96 participants | 3 participants | 55 participants | 78 participants | 92 participants | 104 participants | 41 participants | 43 participants | 42 participants | 1131 participants | |
Female |
18 100.0%
|
3 100.0%
|
18 100.0%
|
14 23.7%
|
1 33.3%
|
15 30.6%
|
7 13.5%
|
5 27.8%
|
2 66.7%
|
8 44.4%
|
12 40.0%
|
37 37.8%
|
26 42.6%
|
61 41.5%
|
35 36.5%
|
1 33.3%
|
23 41.8%
|
24 30.8%
|
18 19.6%
|
23 22.1%
|
41 100.0%
|
43 100.0%
|
42 100.0%
|
477 42.2%
|
|
Male |
0 0.0%
|
0 0.0%
|
0 0.0%
|
45 76.3%
|
2 66.7%
|
34 69.4%
|
45 86.5%
|
13 72.2%
|
1 33.3%
|
10 55.6%
|
18 60.0%
|
61 62.2%
|
35 57.4%
|
86 58.5%
|
61 63.5%
|
2 66.7%
|
32 58.2%
|
54 69.2%
|
74 80.4%
|
81 77.9%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
654 57.8%
|
|
[1]
Measure Analysis Population Description: All treated Participants
|
|||||||||||||||||||||||||
Ethnicity (NIH/OMB)
[1] Measure Type: Count of Participants Unit of measure: Participants |
|||||||||||||||||||||||||
Number Analyzed | 18 participants | 3 participants | 18 participants | 59 participants | 3 participants | 49 participants | 52 participants | 18 participants | 3 participants | 18 participants | 30 participants | 98 participants | 61 participants | 147 participants | 96 participants | 3 participants | 55 participants | 78 participants | 92 participants | 104 participants | 41 participants | 43 participants | 42 participants | 1131 participants | |
Hispanic or Latino |
0 0.0%
|
0 0.0%
|
0 0.0%
|
1 1.7%
|
0 0.0%
|
1 2.0%
|
2 3.8%
|
0 0.0%
|
0 0.0%
|
1 5.6%
|
0 0.0%
|
3 3.1%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
1 1.8%
|
2 2.6%
|
0 0.0%
|
4 3.8%
|
1 2.4%
|
1 2.3%
|
1 2.4%
|
18 1.6%
|
|
Not Hispanic or Latino |
10 55.6%
|
3 100.0%
|
9 50.0%
|
41 69.5%
|
2 66.7%
|
29 59.2%
|
35 67.3%
|
16 88.9%
|
3 100.0%
|
13 72.2%
|
28 93.3%
|
63 64.3%
|
47 77.0%
|
97 66.0%
|
55 57.3%
|
2 66.7%
|
26 47.3%
|
59 75.6%
|
38 41.3%
|
73 70.2%
|
26 63.4%
|
29 67.4%
|
32 76.2%
|
736 65.1%
|
|
Unknown or Not Reported |
8 44.4%
|
0 0.0%
|
9 50.0%
|
17 28.8%
|
1 33.3%
|
19 38.8%
|
15 28.8%
|
2 11.1%
|
0 0.0%
|
4 22.2%
|
2 6.7%
|
32 32.7%
|
14 23.0%
|
50 34.0%
|
41 42.7%
|
1 33.3%
|
28 50.9%
|
17 21.8%
|
54 58.7%
|
27 26.0%
|
14 34.1%
|
13 30.2%
|
9 21.4%
|
377 33.3%
|
|
[1]
Measure Analysis Population Description: All Treated Participants
|
|||||||||||||||||||||||||
Race (NIH/OMB)
[1] Measure Type: Count of Participants Unit of measure: Participants |
|||||||||||||||||||||||||
Number Analyzed | 18 participants | 3 participants | 18 participants | 59 participants | 3 participants | 49 participants | 52 participants | 18 participants | 3 participants | 18 participants | 30 participants | 98 participants | 61 participants | 147 participants | 96 participants | 3 participants | 55 participants | 78 participants | 92 participants | 104 participants | 41 participants | 43 participants | 42 participants | 1131 participants | |
American Indian or Alaska Native |
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
1 1.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
1 0.1%
|
|
Asian |
1 5.6%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
1 2.0%
|
0 0.0%
|
1 5.6%
|
0 0.0%
|
1 5.6%
|
1 3.3%
|
1 1.0%
|
0 0.0%
|
2 1.4%
|
1 1.0%
|
0 0.0%
|
0 0.0%
|
1 1.3%
|
1 1.1%
|
4 3.8%
|
2 4.9%
|
0 0.0%
|
1 2.4%
|
18 1.6%
|
|
Native Hawaiian or Other Pacific Islander |
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
|
Black or African American |
3 16.7%
|
0 0.0%
|
1 5.6%
|
3 5.1%
|
0 0.0%
|
1 2.0%
|
1 1.9%
|
1 5.6%
|
0 0.0%
|
1 5.6%
|
4 13.3%
|
3 3.1%
|
1 1.6%
|
7 4.8%
|
5 5.2%
|
1 33.3%
|
0 0.0%
|
4 5.1%
|
3 3.3%
|
4 3.8%
|
1 2.4%
|
0 0.0%
|
2 4.8%
|
46 4.1%
|
|
White |
14 77.8%
|
3 100.0%
|
17 94.4%
|
56 94.9%
|
3 100.0%
|
46 93.9%
|
50 96.2%
|
16 88.9%
|
3 100.0%
|
16 88.9%
|
23 76.7%
|
91 92.9%
|
60 98.4%
|
134 91.2%
|
87 90.6%
|
2 66.7%
|
54 98.2%
|
72 92.3%
|
87 94.6%
|
90 86.5%
|
37 90.2%
|
43 100.0%
|
38 90.5%
|
1042 92.1%
|
|
More than one race |
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
|
Unknown or Not Reported |
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
1 2.0%
|
1 1.9%
|
0 0.0%
|
0 0.0%
|
0 0.0%
|
2 6.7%
|
2 2.0%
|
0 0.0%
|
4 2.7%
|
3 3.1%
|
0 0.0%
|
1 1.8%
|
1 1.3%
|
1 1.1%
|
6 5.8%
|
1 2.4%
|
0 0.0%
|
1 2.4%
|
24 2.1%
|
|
[1]
Measure Analysis Population Description: All Treated Participnats
|
Outcome Measures
Adverse Events