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Reopro (ABCIXIMAB)

Johnson & Johnson · FDA-approved approved Monoclonal antibody Quality 30/100

Reopro (abciximab) is a medication originally developed by Centocor Inc, currently owned by the same company. It targets the integrin alpha-IIb/beta-3, a protein involved in platelet aggregation. Reopro is used to treat patients undergoing percutaneous coronary intervention, and it was FDA-approved in 1993. The commercial status of Reopro is patented, and it is not yet available as a generic medication. Key safety considerations include bleeding risks and allergic reactions.

At a glance

Generic nameABCIXIMAB
SponsorJohnson & Johnson
TargetIntegrin alpha-IIb/beta-3
ModalityMonoclonal antibody
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1993

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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