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umeclidinium 62.5 µg and vilanterol 25 µg
umeclidinium 62.5 µg and vilanterol 25 µg is a Long-acting anticholinergic and long-acting beta-2 agonist combination (LAMA/LABA) Small molecule drug developed by University of Tennessee Graduate School of Medicine. It is currently FDA-approved for Chronic obstructive pulmonary disease (COPD) maintenance treatment. Also known as: Anoro Ellipta.
Umeclidinium is a long-acting anticholinergic that blocks muscarinic M3 receptors in airway smooth muscle, while vilanterol is a long-acting beta-2 agonist that activates beta-2 adrenergic receptors, together producing bronchodilation for maintenance treatment of chronic obstructive pulmonary disease.
Umeclidinium is a long-acting anticholinergic that blocks muscarinic M3 receptors in airway smooth muscle, while vilanterol is a long-acting beta-2 agonist that activates beta-2 adrenergic receptors, together producing bronchodilation for maintenance treatment of chronic obstructive pulmonary disease. Used for Chronic obstructive pulmonary disease (COPD) maintenance treatment.
At a glance
| Generic name | umeclidinium 62.5 µg and vilanterol 25 µg |
|---|---|
| Also known as | Anoro Ellipta |
| Sponsor | University of Tennessee Graduate School of Medicine |
| Drug class | Long-acting anticholinergic and long-acting beta-2 agonist combination (LAMA/LABA) |
| Target | Muscarinic M3 receptor (umeclidinium); Beta-2 adrenergic receptor (vilanterol) |
| Modality | Small molecule |
| Therapeutic area | Respiratory/Pulmonology |
| Phase | FDA-approved |
Mechanism of action
Umeclidinium prevents acetylcholine from binding to M3 receptors on airway smooth muscle, reducing bronchoconstriction. Vilanterol activates beta-2 adrenergic receptors, increasing intracellular cAMP and promoting smooth muscle relaxation. The combination provides dual bronchodilation through complementary mechanisms, improving airflow and reducing symptoms in COPD patients.
Approved indications
- Chronic obstructive pulmonary disease (COPD) maintenance treatment
Common side effects
- Tremor
- Headache
- Palpitations
- Dry mouth
- Urinary retention
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:
- umeclidinium 62.5 µg and vilanterol 25 µg CI brief — competitive landscape report
- umeclidinium 62.5 µg and vilanterol 25 µg updates RSS · CI watch RSS
- University of Tennessee Graduate School of Medicine portfolio CI
Frequently asked questions about umeclidinium 62.5 µg and vilanterol 25 µg
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Related
- Drug class: All Long-acting anticholinergic and long-acting beta-2 agonist combination (LAMA/LABA) drugs
- Target: All drugs targeting Muscarinic M3 receptor (umeclidinium); Beta-2 adrenergic receptor (vilanterol)
- Manufacturer: University of Tennessee Graduate School of Medicine — full pipeline
- Therapeutic area: All drugs in Respiratory/Pulmonology
- Indication: Drugs for Chronic obstructive pulmonary disease (COPD) maintenance treatment
- Also known as: Anoro Ellipta
- Compare: umeclidinium 62.5 µg and vilanterol 25 µg vs similar drugs
- Pricing: umeclidinium 62.5 µg and vilanterol 25 µg cost, discount & access