Skip to content

PPI and Clopidogrel Response

Effects of PPI Therapy on Clopidogrel-Induced Antiplatelet Effects: A Randomized Study

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01170533
Enrollment
20
Registered
2010-07-27
Start date
2009-03-31
Completion date
2010-08-31
Last updated
2012-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Drug Interaction

Keywords

proton pump inhibitor, clopidogrel, platelet function

Brief summary

Clopidogrel, in combination with aspirin, is currently the recommended treatment for secondary prevention of ischemic events in high-risk patients and for prevention of coronary artery stent thrombosis. Patients receiving aspirin and clopidogrel are frequently treated with proton pump inhibitors, such as omeprazole or pantoprazole, in order to prevent the risk of gastrointestinal bleeding, accorded to guidelines. An interaction between proton pump inhibitors and clopidogrel has been suggested, which may lead to a decrease of clopidogrel effects. It remains unclear whether this interaction between PPIs and clopidogrel might be a class effect or if this may be affected by timing regimen. The objectives of this two-phase investigation are: 1. to compare clopidogrel platelet inhibitory effects when taken at the same time versus separated at least 8 hours from omeprazole administration. 2. to compare clopidogrel-induced inhibitory effects when taken at the same time versus staggered at least 8 hours from pantoprazole administration.

Detailed description

Clopidogrel, in combination with aspirin, is currently the recommended treatment for secondary prevention of ischemic events in high-risk patients and for prevention of coronary artery stent thrombosis. Patients receiving aspirin and clopidogrel are frequently treated with proton pump inhibitors, such as omeprazole or pantoprazole, in order to prevent the risk of gastrointestinal bleeding, accorded to guidelines. An interaction between proton pump inhibitors and clopidogrel has been suggested, which may lead to a decrease of clopidogrel effects. It remains unclear whether this interaction between PPIs and clopidogrel might be a class effect or if this may be affected by timing regimen. The objectives of this two-phase investigation are: 1. to compare clopidogrel platelet inhibitory effects when taken at the same time versus separated at least 8 hours from omeprazole administration. 2. to compare clopidogrel-induced inhibitory effects when taken at the same time versus staggered at least 8 hours from pantoprazole administration. The clopidogrel dose will be a 600mg loading dose followed by a 75mg daily maintenance dose, starting the next day for 7 days. Omeprazole will be used at a daily dose of 40mg and pantoprazole at 80mg. The proposed study will have a prospective, randomized, cross-over design. Subjects are randomized in a 1:1 fashion to take PPI concomitantly (CONC regimen) or staggered by 8-12 hours (STAG regimen) for one-week on a background of clopidogrel therapy. In particular, in the CONC regimen both drugs were taken in the morning, while in the STAG regimen clopidogrel was taken in the morning and omeprazole in the evening. After a 2-4 week washout period, subjects crossed-over treatment regimen. After completing these two treatment phases, subjects underwent another washout period of 2-4 weeks and were treated for 1 week with clopidogrel alone, without receiving omeprazole therapy (CLOP regimen). The sequence with the PPI pantoprazole will have the same prospective, randomized, cross-over design as the omeprazole sequence. A CLOP regimen in the absence of pantoprazole will be collected before entering randomization phase with adequate wash-out period. Blood sampling for platelet function assessments were performed at all three phases of the study at the following time points: a) baseline, b) 24 hours after LD (before intake of study medication), and c) 7 days (24 hours after the last MD).

Interventions

DRUGomeprazole and pantoprazole

The clopidogrel dose will be a 600mg loading dose followed by a 75mg daily maintenance dose, starting the next day for 7 days. Omeprazole will be used at a daily dose of 40mg and pantoprazole at 80mg.

Sponsors

Bristol-Myers Squibb
CollaboratorINDUSTRY
Sanofi
CollaboratorINDUSTRY
University of Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy volunteers aged between 18 and 75 years

Exclusion criteria

1. Known allergies to clopidogrel or omeprazole. 2. Blood dyscrasia or bleeding diathesis. 3. Recent antiplatelet treatment (\< 30 days) with a glycoprotein IIb/IIIa antagonist, thienopyridine (ticlopidine, clopidogrel), cilostazol or dipyridamole. 4. Treatment with other medications that may interfere with the CYP system (ketoconazole, itraconazole, diltiazem, erythromycin, clarithromycin, fluvoxamine, fluoxetine, nefazodone, or sertraline). 5. Platelet count \<100x106/microL. 6. Diabetes mellitus 7. History of coronary artery disease, gastrointestinal bleed, gastroesophageal reflux disease (GERD), cerebrovascular event or any active malignancy. 8. Active bleeding or hemodynamic instability. 9. Serum creatinine \>2mg/dL. 10. Baseline ALT \>2.5 times the upper limit of normal. 11. Pregnant females. 12. Patients taking omeprazole or any H2 antagonist or proton pump inhibitors

Design outcomes

Primary

MeasureTime frameDescription
Platelet Function as Assessed by the P2Y12 Reactivity Index1 weekP2Y12 reactivity index which will be assessed by flow cytometry determination of vasodilator-stimulated phosphoprotein (VASP).

Countries

United States

Participant flow

Pre-assignment details

The proposed study will have a prospective, randomized, cross-over design.

Participants by arm

ArmCount
All Study Participants
This was a prospective, open-label, two-sequence, three-period, randomized crossover study conducted in non-medicated healthy male subjects between the ages of 18 and 65 years. Subjects were randomized in a 1:1 fashion to take a PPI concomitantly (CONC) or staggered (STAG) by 8-12 hours for one-week on a background of clopidogrel therapy. In particular, in the CONC regimen both drugs were taken in the morning, while in the STAG regimen clopidogrel was taken in the morning and the PPI in the evening. After a 2-4 week washout period, subjects crossed-over treatment regimen. After completing these two treatment phases, subjects underwent another washout period of 2-4 weeks and were treated for 1 week with clopidogrel alone, without receiving PPI therapy (CLOP regimen). The PPI could be omeprazole (first phase) or pantoprazole (second phase).
25
Total25

Baseline characteristics

CharacteristicAll Study Participants
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
25 Participants
Age Continuous
Omeprazole cross-over n=20
34 years
STANDARD_DEVIATION 6
Age Continuous
Pantoprazole cross-over n=20
33 years
STANDARD_DEVIATION 5
Region of Enrollment
United States
25 participants
Sex: Female, Male
Female
0 Participants
Sex: Female, Male
Male
25 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 200 / 20
serious
Total, serious adverse events
0 / 200 / 20

Outcome results

Primary

Platelet Function as Assessed by the P2Y12 Reactivity Index

P2Y12 reactivity index which will be assessed by flow cytometry determination of vasodilator-stimulated phosphoprotein (VASP).

Time frame: 1 week

Population: A sample size of 18 patients was required to be able to detect a 10% absolute difference in PRI between both regimens with 80% power and 2-sided significance level of 0.05, assuming a 15% standard deviation for the difference between regimens.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
Omeprazole ConcomitantPlatelet Function as Assessed by the P2Y12 Reactivity Index56.1 Percentage of platelet reactivity indexStandard Error 3.5
Omeprazole StaggeredPlatelet Function as Assessed by the P2Y12 Reactivity Index61.6 Percentage of platelet reactivity indexStandard Error 3.4
Pantoprazole ConcomitantPlatelet Function as Assessed by the P2Y12 Reactivity Index56 Percentage of platelet reactivity indexStandard Error 3.9
Pantoprazole StaggeredPlatelet Function as Assessed by the P2Y12 Reactivity Index61 Percentage of platelet reactivity indexStandard Error 3.9
Clopidogrel Only (Omeprazole Phase)Platelet Function as Assessed by the P2Y12 Reactivity Index48.8 Percentage of platelet reactivity indexStandard Error 3.4
Clopidogrel Only (Pantoprazole Phase)Platelet Function as Assessed by the P2Y12 Reactivity Index61.0 Percentage of platelet reactivity indexStandard Error 3.9

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026