Last reviewed · How we verify
Pitavastin 4mg
Pitavastin 4mg is a Statins Small molecule drug developed by University of Kansas Medical Center. It is currently FDA-approved. Also known as: Livalo.
Pitavastatin 4mg is used to treat hypercholesterolemia, a condition characterized by high levels of cholesterol in the blood. It works by inhibiting HMG-CoA reductase, an enzyme involved in cholesterol production, as indicated by its classification in ChEMBL.
At a glance
| Generic name | Pitavastin 4mg |
|---|---|
| Also known as | Livalo |
| Sponsor | University of Kansas Medical Center |
| Drug class | Statins |
| Target | HMG-CoA reductase |
| Modality | Small molecule |
| Therapeutic area | Metabolic |
| Phase | FDA-approved |
Approved indications
Pipeline indications
Common side effects
Drug interactions
- Cyclosporine
- Gemfibrozil
- Erythromycin
- Itraconazole
Key clinical trials
Patents
| Patent | Expiry | Type |
|---|---|---|
| US12345678 |
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 |
| FDA Orange Book | Patents + exclusivity |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Pitavastin 4mg CI brief — competitive landscape report
- Pitavastin 4mg updates RSS · CI watch RSS
- University of Kansas Medical Center portfolio CI
Frequently asked questions about Pitavastin 4mg
What is Pitavastin 4mg?
Who makes Pitavastin 4mg?
Is Pitavastin 4mg also known as anything else?
What drug class is Pitavastin 4mg in?
What development phase is Pitavastin 4mg in?
What does Pitavastin 4mg target?
Related
- Drug class: All Statins drugs
- Target: All drugs targeting HMG-CoA reductase
- Manufacturer: University of Kansas Medical Center — full pipeline
- Therapeutic area: All drugs in Metabolic
- Also known as: Livalo
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing