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Comparison of Generic and Original Formulation of Clopidogrel

Comparison of the Generic and Original Formulation of Clopidogrel Regarding the Potency of Platelet Inhibition in Patients After PCI

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01147133
Acronym
DOSER-GENERIC
Enrollment
75
Registered
2010-06-22
Start date
2009-11-30
Completion date
2010-05-31
Last updated
2013-01-29

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

Conditions

Coronary Heart Disease, Percutaneous Coronary Intervention

Keywords

Platelet aggregation, Generic, Clopidogrel, Comparison, VASP-PRI

Brief summary

Clopidogrel is essential for the prevention of vascular events in patients after percutaneous coronary interventions (PCI). Most of our current knowledge with clopidogrel originates from the clinical investigations that had used Plavix®/Iscover® from Sanofi-Aventis as the original formulation of clopidogrel-bisulphate. However, as the patency of Plavix® has expired in November 2009 in Hungary, several generic clopidogrel have been introduced to the market. Some of the generics are using the original bisulphate formulation, while others are with besylate salt of clopidogrel. Despite the differences in the clopidogrel-salts, the different carriers might also modulate the pharmacokinetic/pharmacodynamic profile of each drug. As the consequences of the impaired antiplatelet potency might be devastating, including stent thrombosis, the investigators sought to compare generic clopidogrel to the original blister by different assays of platelet aggregation.

Detailed description

Clopidogrel is essential for the prevention of vascular events in patients after percutaneous coronary interventions (PCI). Most of our current knowledge with clopidogrel originates from the clinical investigations that had used Plavix®/Iscover® from Sanofi-Aventis as the original formulation of clopidogrel-bisulphate. However, as the patency of Plavix® has expired in November 2009 in Hungary, several generic clopidogrel have been introduced to the market. Some of the generics are using the original bisulphate formulation, while others are with besylate salt of clopidogrel. Despite the differences in the clopidogrel-salts, the different carriers might also modulate the pharmacokinetic/pharmacodynamic profile of each drug. As the consequences of the impaired antiplatelet potency might be devastating, including stent thrombosis, the investigators sought to compare generic clopidogrel to the original blister by different assays of platelet aggregation. In a prospective, cross-over, open-label, unblinded study the investigators aim to compare platelet activation and aggregation between Plavix® and generic clopidogrel.

Interventions

DRUGPlavix

1x75 mg

DRUGKardogrel

1x75 mg

Sponsors

Hungarian Academy of Sciences
CollaboratorOTHER
KRKA
CollaboratorINDUSTRY
University of Pecs
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients in the maintenance phase of PCI receiving 1x75 mg clopidogrel and 1x100 mg aspirin * No planned interruption of the antiplatelet therapy in the next 1 month * Informed consent

Exclusion criteria

* Oral anticoagulant therapy * Contraindication for aspirin or clopidogrel * Planned interruption of antiplatelet therapy in the next month

Design outcomes

Primary

MeasureTime frame
ADP 5 microM-induced maximal aggregation in light transmission aggregometry between the two time point.14 days

Secondary

MeasureTime frame
VASP-PRI (%) 6-minute late aggregation with LTA (%) Proportion of patients with high platelet reactivity (HPR)14 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026