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Aspirin 80
Aspirin 80 is a Nonsteroidal anti-inflammatory drug (NSAID); antiplatelet agent Small molecule drug developed by Shiraz University of Medical Sciences. It is currently FDA-approved for Acute myocardial infarction prevention, Ischemic stroke prevention, Transient ischemic attack (TIA) prevention.
Aspirin irreversibly inhibits cyclooxygenase (COX) enzymes, reducing the production of thromboxane A2 and other prostaglandins to decrease platelet aggregation and inflammation.
Aspirin irreversibly inhibits cyclooxygenase (COX) enzymes, reducing the production of thromboxane A2 and other prostaglandins to decrease platelet aggregation and inflammation. Used for Acute myocardial infarction prevention, Ischemic stroke prevention, Transient ischemic attack (TIA) prevention.
At a glance
| Generic name | Aspirin 80 |
|---|---|
| Sponsor | Shiraz University of Medical Sciences |
| Drug class | Nonsteroidal anti-inflammatory drug (NSAID); antiplatelet agent |
| Target | Cyclooxygenase-1 (COX-1); Cyclooxygenase-2 (COX-2) |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
Mechanism of action
Aspirin acetylates serine residues on COX-1 and COX-2 enzymes, permanently blocking their catalytic activity. This prevents the synthesis of thromboxane A2 in platelets, which is essential for platelet activation and clot formation. At low doses (such as 80 mg), aspirin preferentially affects platelet function, making it effective for antiplatelet therapy without significantly inhibiting protective prostaglandins in the gastrointestinal tract.
Approved indications
- Acute myocardial infarction prevention
- Ischemic stroke prevention
- Transient ischemic attack (TIA) prevention
- Stable angina pectoris
Common side effects
- Gastrointestinal bleeding
- Dyspepsia
- Nausea
- Hemorrhagic stroke
- Allergic reactions
Key clinical trials
- IRELAnD: Investigating the Role of Early Low-dose Aspirin in Diabetes (PHASE3)
- Short-Term Anticoagulation Versus Antiplatelet Therapy for Preventing Device Thrombosis Following Left Atrial Appendage Closure (PHASE4)
- PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated Stroke in Patients Aged 60 to 80 Years (PHASE3)
- Rivaroxaban vs Warfarin in Patients With Mechanical Heart Valves (PHASE3)
- Aspirin-free Strategy With Ticagrelor in Patients With a Myocardial Infarction Treated Medically Alone (PHASE3)
- Testing a New Treatment Strategy to Improve Secondary Stroke Prevention for Older Adults: The STROKE75+ Trial (PHASE3)
- Gut Microbiota in Acute Stroke Patients
- Women's IschemiA TRial to Reduce Events In Non-ObstRuctive CAD (PHASE4)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Aspirin 80 CI brief — competitive landscape report
- Aspirin 80 updates RSS · CI watch RSS
- Shiraz University of Medical Sciences portfolio CI
Frequently asked questions about Aspirin 80
What is Aspirin 80?
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Related
- Drug class: All Nonsteroidal anti-inflammatory drug (NSAID); antiplatelet agent drugs
- Target: All drugs targeting Cyclooxygenase-1 (COX-1); Cyclooxygenase-2 (COX-2)
- Manufacturer: Shiraz University of Medical Sciences — full pipeline
- Therapeutic area: All drugs in Cardiovascular
- Indication: Drugs for Acute myocardial infarction prevention
- Indication: Drugs for Ischemic stroke prevention
- Indication: Drugs for Transient ischemic attack (TIA) prevention
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing