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Nitrendipine/Atenolol
This combination drug reduces blood pressure by blocking calcium channels (nitrendipine) to relax blood vessels and blocking beta-adrenergic receptors (atenolol) to reduce heart rate and cardiac output.
This combination drug reduces blood pressure by blocking calcium channels (nitrendipine) to relax blood vessels and blocking beta-adrenergic receptors (atenolol) to reduce heart rate and cardiac output. Used for Hypertension.
At a glance
| Generic name | Nitrendipine/Atenolol |
|---|---|
| Also known as | Nitrendipine and Atenolol Tablets |
| Sponsor | Shanghai Jiao Tong University School of Medicine |
| Drug class | Calcium channel blocker / Beta-blocker combination |
| Target | L-type calcium channels; Beta-1 adrenergic receptor |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
Mechanism of action
Nitrendipine is a dihydropyridine calcium channel blocker that inhibits L-type calcium channels in vascular smooth muscle, causing vasodilation and reduced peripheral vascular resistance. Atenolol is a selective beta-1 adrenergic antagonist that decreases heart rate, contractility, and blood pressure. The combination provides complementary antihypertensive effects through different mechanisms.
Approved indications
- Hypertension
Common side effects
- Headache
- Dizziness
- Fatigue
- Peripheral edema
- Bradycardia
- Flushing
Key clinical trials
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:
- Nitrendipine/Atenolol CI brief — competitive landscape report
- Nitrendipine/Atenolol updates RSS · CI watch RSS
- Shanghai Jiao Tong University School of Medicine portfolio CI