NDAORALSUSPENSION
Approved
Jun 2004
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
3/8 — Basic
MELOXICAM (meloxicam) by Ascentage Pharma is cyclooxygenase inhibitors [moa]. First approved in 2004.
Drug data last refreshed 6h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Meloxicam is an oral NSAID suspension that inhibits cyclooxygenase enzymes to reduce inflammation and pain. It is used to treat inflammatory conditions, though specific indications are not detailed in available data. The drug works as a small-molecule COX inhibitor targeting inflammatory pathways.
LOE Approaching
As a near-LOE product, expect a smaller, defensive team focused on maintaining market share against generics rather than expansion.
Mechanism of Action
Cyclooxygenase Inhibitors
Pharmacologic Class:
Nonsteroidal Anti-inflammatory Drug
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Oral Levonorgestrel Plus Meloxicam, IG-002 Delays Ovulation in Normal Menstruating Women by Seven Days
Started Jun 2022
19 enrolled
Pregnancy Prevention
A Study to Compare the Amount of Meloxicam in the Blood When it is Taken as Capsules or as Tablets
Started Oct 2018
26 enrolled
Healthy
This Study is Randomised, Single Oral Dose Bioequivalence Study of Meloxicam GSK 15 MG Tablets.
Started Sep 2013
28 enrolled
Arthritis, Rheumatoid
Effect Of Meloxicam Versus Placebo In Mainland Chinese Patients With Osteoarthritis Of The Knee
Started Oct 2011
408 enrolled
Osteoarthritis of the Knee
Bioequivalence Study of Meloxicam Capsules 15 mg (Mobic® Capsules 15 mg) Versus Meloxicam Tablets 15 mg (Mobic® Tablets 15 mg) in Healthy Adult Volunteers
Started Nov 2008
6 enrolled
Healthy
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.