Trial Outcomes & Findings for Efficacy and Safety of Low-dose Ticagrelor (NCT NCT03381742)
NCT ID: NCT03381742
Last Updated: 2019-09-30
Results Overview
The venous blood samples for platelet function test were drawn after an overnight fast, at 12 hours post-last study-drug dose for subjects receiving twice-daily administrations, and at 24 hours post-last study-drug dose for subjects treated with once-daily regimens. The blood was collected in an evacuated vacuum tube containing 3.2% trisodium citrate and lithium heparin. Then the samples were processed within two hours of blood draw according to standard operating procedure. The physical properties of samples were analyzed using Thromboelastography (TEG) Hemostasis Analyzer (CFMS LEPU-8800, Lepu Medical Technology Co., Ltd, Beijing, China) and automated analytical software. TEG test used four channels to detect the effects of anti-platelet therapy via the arachidonic acid (AA) and ADP pathways. TEG test results were expressed in terms of ADP-induced inhibition of platelet aggregation (IPA, range 0% - 100%), with higher values indicating greater platelet inhibition.
COMPLETED
PHASE2/PHASE3
3043 participants
up to 5 days
2019-09-30
Participant Flow
3,737 CAD patients who received either clopidogrel or ticagrelor therapy and underwent TEG test from 11 medical centers. Among these patients, 1,725 subjects were treated with clopidogrel and 2,012 subjects were treated with different ticagrelor regimens.
Participant milestones
| Measure |
Ticagrelor 45mg Bidpo.
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Clopidogrel 75mg Qdpo.
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
|---|---|---|---|---|
|
Overall Study
STARTED
|
525
|
501
|
1511
|
506
|
|
Overall Study
COMPLETED
|
525
|
501
|
1511
|
506
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Efficacy and Safety of Low-dose Ticagrelor
Baseline characteristics by cohort
| Measure |
Clopidogrel 75mg Qdpo.
n=1511 Participants
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
n=501 Participants
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 45mg Bidpo.
n=525 Participants
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
n=506 Participants
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
Total
n=3043 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|
|
Age, Continuous
|
63 years
n=99 Participants
|
61 years
n=107 Participants
|
62 years
n=206 Participants
|
62 years
n=7 Participants
|
62 years
n=31 Participants
|
|
Sex: Female, Male
Female
|
532 Participants
n=99 Participants
|
159 Participants
n=107 Participants
|
201 Participants
n=206 Participants
|
237 Participants
n=7 Participants
|
1129 Participants
n=31 Participants
|
|
Sex: Female, Male
Male
|
979 Participants
n=99 Participants
|
342 Participants
n=107 Participants
|
324 Participants
n=206 Participants
|
269 Participants
n=7 Participants
|
1914 Participants
n=31 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
|
Race (NIH/OMB)
Asian
|
1511 Participants
n=99 Participants
|
501 Participants
n=107 Participants
|
525 Participants
n=206 Participants
|
506 Participants
n=7 Participants
|
3043 Participants
n=31 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
|
Race (NIH/OMB)
Black or African American
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
|
Race (NIH/OMB)
White
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
|
Region of Enrollment
China
|
1511 participants
n=99 Participants
|
501 participants
n=107 Participants
|
525 participants
n=206 Participants
|
506 participants
n=7 Participants
|
3043 participants
n=31 Participants
|
|
Weight
|
70 kg
n=99 Participants
|
70 kg
n=107 Participants
|
70 kg
n=206 Participants
|
70 kg
n=7 Participants
|
70 kg
n=31 Participants
|
|
smoking
|
736 Participants
n=99 Participants
|
234 Participants
n=107 Participants
|
226 Participants
n=206 Participants
|
202 Participants
n=7 Participants
|
1398 Participants
n=31 Participants
|
|
Hypertension
|
879 Participants
n=99 Participants
|
243 Participants
n=107 Participants
|
332 Participants
n=206 Participants
|
287 Participants
n=7 Participants
|
1741 Participants
n=31 Participants
|
|
diabetes mellitus
|
426 Participants
n=99 Participants
|
126 Participants
n=107 Participants
|
161 Participants
n=206 Participants
|
117 Participants
n=7 Participants
|
830 Participants
n=31 Participants
|
|
chronic kidney disease
|
60 Participants
n=99 Participants
|
13 Participants
n=107 Participants
|
25 Participants
n=206 Participants
|
13 Participants
n=7 Participants
|
111 Participants
n=31 Participants
|
|
percutaneous coronary intervention
|
1056 Participants
n=99 Participants
|
326 Participants
n=107 Participants
|
241 Participants
n=206 Participants
|
179 Participants
n=7 Participants
|
1802 Participants
n=31 Participants
|
|
coronary artery bypass grafting
|
12 Participants
n=99 Participants
|
2 Participants
n=107 Participants
|
2 Participants
n=206 Participants
|
1 Participants
n=7 Participants
|
17 Participants
n=31 Participants
|
|
total cholesterol
|
4.2 mmol/L
n=99 Participants
|
3.9 mmol/L
n=107 Participants
|
4.3 mmol/L
n=206 Participants
|
4.7 mmol/L
n=7 Participants
|
4.24 mmol/L
n=31 Participants
|
|
triglyceride
|
1.6 mmol/L
n=99 Participants
|
1.9 mmol/L
n=107 Participants
|
1.7 mmol/L
n=206 Participants
|
1.6 mmol/L
n=7 Participants
|
1.67 mmol/L
n=31 Participants
|
|
high density lipoprotein
|
1.1 mmol/L
n=99 Participants
|
1.1 mmol/L
n=107 Participants
|
1.1 mmol/L
n=206 Participants
|
1.2 mmol/L
n=7 Participants
|
1.1 mmol/L
n=31 Participants
|
|
low density lipoprotein
|
2.6 mmol/L
n=99 Participants
|
2.8 mmol/L
n=107 Participants
|
2.7 mmol/L
n=206 Participants
|
2.9 mmol/L
n=7 Participants
|
2.68 mmol/L
n=31 Participants
|
|
creatinine
|
71 μmol/L
n=99 Participants
|
69.7 μmol/L
n=107 Participants
|
68.7 μmol/L
n=206 Participants
|
67.7 μmol/L
n=7 Participants
|
69.9 μmol/L
n=31 Participants
|
|
uric acid
|
330 μmol/L
n=99 Participants
|
338 μmol/L
n=107 Participants
|
323 μmol/L
n=206 Participants
|
320 μmol/L
n=7 Participants
|
328.4 μmol/L
n=31 Participants
|
|
aspirin use
|
1429 Participants
n=99 Participants
|
446 Participants
n=107 Participants
|
475 Participants
n=206 Participants
|
443 Participants
n=7 Participants
|
2793 Participants
n=31 Participants
|
|
acute myocardial infarction
|
568 Participants
n=99 Participants
|
180 Participants
n=107 Participants
|
98 Participants
n=206 Participants
|
49 Participants
n=7 Participants
|
895 Participants
n=31 Participants
|
PRIMARY outcome
Timeframe: up to 5 daysThe venous blood samples for platelet function test were drawn after an overnight fast, at 12 hours post-last study-drug dose for subjects receiving twice-daily administrations, and at 24 hours post-last study-drug dose for subjects treated with once-daily regimens. The blood was collected in an evacuated vacuum tube containing 3.2% trisodium citrate and lithium heparin. Then the samples were processed within two hours of blood draw according to standard operating procedure. The physical properties of samples were analyzed using Thromboelastography (TEG) Hemostasis Analyzer (CFMS LEPU-8800, Lepu Medical Technology Co., Ltd, Beijing, China) and automated analytical software. TEG test used four channels to detect the effects of anti-platelet therapy via the arachidonic acid (AA) and ADP pathways. TEG test results were expressed in terms of ADP-induced inhibition of platelet aggregation (IPA, range 0% - 100%), with higher values indicating greater platelet inhibition.
Outcome measures
| Measure |
Clopidogrel 75mg Qdpo.
n=1511 Participants
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
n=501 Participants
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 45mg Bidpo.
n=525 Participants
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
n=506 Participants
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
|---|---|---|---|---|
|
ADP-induced Inhibition of Platelet Aggregation
|
54.9 percentage of inhibition of platelet agg
Interval 31.9 to 79.1
|
80.6 percentage of inhibition of platelet agg
Interval 64.1 to 94.0
|
73.6 percentage of inhibition of platelet agg
Interval 52.6 to 93.7
|
66 percentage of inhibition of platelet agg
Interval 46.9 to 87.0
|
PRIMARY outcome
Timeframe: up to 5 daysMajor bleeding was defined as type ≥ 3 and minor bleeding as types 1 and 2, in accordance to the Bleeding Academic Research Consortium classification. (Mehran R et al. Standardized bleeding definitions for cardiovascular clinical trials: a consensus report from the Bleeding Academic Research Consortium. Circulation. 2011 Jun 14;123(23):2736-47. doi: 10.1161/CIRCULATIONAHA.110.009449.)
Outcome measures
| Measure |
Clopidogrel 75mg Qdpo.
n=1511 Participants
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
n=501 Participants
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 45mg Bidpo.
n=525 Participants
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
n=506 Participants
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
|---|---|---|---|---|
|
Number of Participants With Bleeding (Major or Minor Bleeding)
Minor bleeding
|
15 Participants
|
30 Participants
|
14 Participants
|
9 Participants
|
|
Number of Participants With Bleeding (Major or Minor Bleeding)
Major bleeding
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
|
Number of Participants With Bleeding (Major or Minor Bleeding)
No bleeding
|
1496 Participants
|
471 Participants
|
511 Participants
|
497 Participants
|
SECONDARY outcome
Timeframe: up to 5 daysThe physical properties of samples were analyzed using Thromboelastography (TEG) Hemostasis Analyzer (CFMS LEPU-8800, Lepu Medical Technology Co., Ltd, Beijing, China) and automated analytical software. TEG test used four channels to detect the effects of anti-platelet therapy via the arachidonic acid (AA) and ADP pathways. TEG test results were expressed in terms of ADP-induced platelet-fibrin clot strength (MA). A MA\>47mm was shown to have a high predictive value for 3-year post-PCI ischemic events during dual antiplatelet therapy. Moreover, ROC curve and quartile analysis suggested MA\<31 mm as a predictive value for post-PCI bleeding events (J Am Coll Cardiol. 2013;62(24):2261-73. doi: 10.1016/j.jacc.2013.07.101.).
Outcome measures
| Measure |
Clopidogrel 75mg Qdpo.
n=1511 Participants
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
n=501 Participants
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 45mg Bidpo.
n=525 Participants
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
n=506 Participants
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
|---|---|---|---|---|
|
ADP-induced Platelet-fibrin Clot Strength (MA)
|
40.3 mm
Interval 27.0 to 51.6
|
28.4 mm
Interval 18.5 to 38.9
|
32.3 mm
Interval 19.5 to 43.9
|
34.05 mm
Interval 23.6 to 46.1
|
SECONDARY outcome
Timeframe: up to 5 daysHTPR was defined as IPA ≤ 30% and MA ≥ 47 mm.
Outcome measures
| Measure |
Clopidogrel 75mg Qdpo.
n=1511 Participants
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
n=501 Participants
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 45mg Bidpo.
n=525 Participants
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
n=506 Participants
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
|---|---|---|---|---|
|
Number of Participants With High On-Treatment Platelet Reactivity (HTPR)
HTPR
|
317 Participants
|
13 Participants
|
23 Participants
|
32 Participants
|
|
Number of Participants With High On-Treatment Platelet Reactivity (HTPR)
Non-HTPR
|
1194 Participants
|
488 Participants
|
502 Participants
|
474 Participants
|
SECONDARY outcome
Timeframe: up to 5 daysCardiovascular death was defined as sudden cardiac death, fatal myocardial infarction, death due to heart failure, or death due to other cardiovascular causes. Stroke was defined as the focal loss of neurologic function caused by an ischemic or a hemorrhagic event with residual symptoms lasting at least 24 hours or eventually leading to death.
Outcome measures
| Measure |
Clopidogrel 75mg Qdpo.
n=1511 Participants
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
n=501 Participants
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 45mg Bidpo.
n=525 Participants
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
n=506 Participants
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
|---|---|---|---|---|
|
Number of Participants With Cardiovascular Event (Cardiovascular Death, New-onset Myocardial Infarction, or Stroke)
Participants with cardiovascular death
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
|
Number of Participants With Cardiovascular Event (Cardiovascular Death, New-onset Myocardial Infarction, or Stroke)
Participants without cardiovascular events
|
1511 Participants
|
501 Participants
|
525 Participants
|
506 Participants
|
|
Number of Participants With Cardiovascular Event (Cardiovascular Death, New-onset Myocardial Infarction, or Stroke)
Participants with new-onset myocardial infarction
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
|
Number of Participants With Cardiovascular Event (Cardiovascular Death, New-onset Myocardial Infarction, or Stroke)
Participants with stroke
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
SECONDARY outcome
Timeframe: up to 5 daysNew-onset dyspnea in patients without previous history of dyspnea
Outcome measures
| Measure |
Clopidogrel 75mg Qdpo.
n=1511 Participants
To observe the efficacy and safety of clopidogrel 75mg qdpo. in patients with coronary artery disease.
clopidogrel: clopidogrel 75 mg once daily for 5 consecutive days at least.
|
Ticagrelor 90mg Bidpo.
n=501 Participants
To observe the efficacy and safety of ticagrelor 90mg bidpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 45mg Bidpo.
n=525 Participants
To observe the efficacy and safety of ticagrelor 45mg bidpo. in patients with coronary artery disease.
Ticagrelor: ticagrelor 45 mg twice daily for 5 consecutive days at least.
|
Ticagrelor 90mg Qdpo.
n=506 Participants
To observe the efficacy and safety of ticagrelor 90mg qdpo. in patients with coronary artery disease.
ticagrelor: ticagrelor 90 mg once daily for 5 consecutive days at least.
|
|---|---|---|---|---|
|
Number of Participants With New-onset Dyspnea
Participants without new-onset dyspne
|
1477 Participants
|
472 Participants
|
493 Participants
|
478 Participants
|
|
Number of Participants With New-onset Dyspnea
Participants with new-onset dyspnea
|
34 Participants
|
29 Participants
|
32 Participants
|
28 Participants
|
Adverse Events
Clopidogrel 75mg Qdpo.
Ticagrelor 90mg Bidpo.
Ticagrelor 45mg Bidpo.
Ticagrelor 90mg Qdpo.
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Dr. Yue Li
Department of Cardiology, the First Affiliated Hospital, Harbin Medical University, Harbin, China
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place