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.

Recruitment status

COMPLETED

Study phase

PHASE2/PHASE3

Target enrollment

3043 participants

Primary outcome timeframe

up to 5 days

Results posted on

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

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

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 days

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.

Outcome measures

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 days

Major 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

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 days

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 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

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 days

HTPR was defined as IPA ≤ 30% and MA ≥ 47 mm.

Outcome measures

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 days

Cardiovascular 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

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 days

New-onset dyspnea in patients without previous history of dyspnea

Outcome measures

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.

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

Ticagrelor 90mg Bidpo.

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

Ticagrelor 45mg Bidpo.

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

Ticagrelor 90mg Qdpo.

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

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

Phone: 86-451-85555673

Results disclosure agreements

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