Last reviewed · How we verify
low-dose atorvastatin
low-dose atorvastatin is a HMG-CoA reductase inhibitor (statin) Small molecule drug developed by Wakayama Medical University. It is currently FDA-approved for Hypercholesterolemia, Cardiovascular disease prevention, Dyslipidemia. Also known as: Lipitor5.
Low-dose atorvastatin inhibits HMG-CoA reductase to reduce cholesterol synthesis and lower LDL cholesterol levels.
Low-dose atorvastatin has been studied in clinical trials for conditions such as hyperlipidemias, contrast-induced acute kidney injury, cardiovascular diseases, coronary artery disease, and HMG-CoA Reductase Inhibitor toxicity. Atorvastatin, a medication that inhibits HMG-CoA reductase, has been evaluated in a phase 1 study (NCT06239714) for its effects on elevated low-density lipoprotein cholesterol (LDL-C).
At a glance
| Generic name | low-dose atorvastatin |
|---|---|
| Also known as | Lipitor5 |
| Sponsor | Wakayama Medical University |
| Drug class | HMG-CoA reductase inhibitor (statin) |
| Target | HMG-CoA reductase |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
Mechanism of action
Atorvastatin is a statin that competitively inhibits HMG-CoA reductase, the rate-limiting enzyme in cholesterol biosynthesis. By reducing hepatic cholesterol production, it lowers circulating LDL cholesterol and triglycerides while modestly increasing HDL cholesterol. Low-dose formulations maintain efficacy while potentially reducing adverse effects associated with higher doses.
Approved indications
- Hypercholesterolemia
- Cardiovascular disease prevention
- Dyslipidemia
Common side effects
- Muscle pain or myalgia
- Elevated liver enzymes
- Headache
- Rhabdomyolysis
Key clinical trials
- Atorvastatin Therapy on Xanthoma in Alagille Syndrome (PHASE4)
- Moderate-intensity Statin vs. Individualized LDL-C Target-based Therapy in Older Adults With Type 2 Diabetes (iTARGET-Elderly Study) (NA)
- Comparison of High and Moderate Intensity Statins in Achieving the Target LDL-C Level After Acute Coronary Syndrome (NA)
- Intensive Lipid-lowering for Plaque and Major Adverse Cardiovascular Events in Low to Intermediate 10-year ASCVD Risk Population (NA)
- A Study of Atorvo+™ in Healthy Adult Participants (PHASE1)
- A Phase II Study to Evaluate the Safety and Efficacy of SAL003 Combined With Atorvastatin in Hypercholesterolemia and Mixed Dyslipidemia (PHASE2)
- Exploring the Impact of Nephropathy Formula No. 1 on Chronic Kidney Disease Patients (EARLY_PHASE1)
- Impact of Statin Therapy on Adaptations to Aerobic Exercise (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:
- low-dose atorvastatin CI brief — competitive landscape report
- low-dose atorvastatin updates RSS · CI watch RSS
- Wakayama Medical University portfolio CI
Frequently asked questions about low-dose atorvastatin
What is low-dose atorvastatin?
How does low-dose atorvastatin work?
What is low-dose atorvastatin used for?
Who makes low-dose atorvastatin?
Is low-dose atorvastatin also known as anything else?
What drug class is low-dose atorvastatin in?
What development phase is low-dose atorvastatin in?
What are the side effects of low-dose atorvastatin?
What does low-dose atorvastatin target?
Related
- Drug class: All HMG-CoA reductase inhibitor (statin) drugs
- Target: All drugs targeting HMG-CoA reductase
- Manufacturer: Wakayama Medical University — full pipeline
- Therapeutic area: All drugs in Cardiovascular
- Indication: Drugs for Hypercholesterolemia
- Indication: Drugs for Cardiovascular disease prevention
- Indication: Drugs for Dyslipidemia
- Also known as: Lipitor5
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing