NDAORALTABLET
Approved
Oct 1957
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
4/8 — Partial
MEDROL (methylprednisolone) by Pfizer is corticosteroid hormone receptor agonists [moa]. First approved in 1957.
Drug data last refreshed 15h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
MEDROL (methylprednisolone) is an oral corticosteroid that works as a glucocorticoid receptor agonist to suppress immune and inflammatory responses. It is used across multiple therapeutic areas including rheumatologic, allergic, dermatologic, and hematologic conditions. The drug has been a cornerstone therapy for over 65 years and remains a standard-of-care option for acute and chronic inflammatory disorders.
$0.011BPart D
LOE ApproachingMEDROL faces LOE pressure with moderate competitive intensity (30), signaling smaller brand teams focused on retention and life-cycle management rather than expansion.
Mechanism of Action
Corticosteroid Hormone Receptor Agonists
Pharmacologic Class:
Corticosteroid
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Efficacy and Safety of Methylprednisolone After Flow-Diverter Stent Implantation in Unruptured Intracranial Aneurysms
Started Jan 2026
864 enrolled
Unruptured Intracranial AneurysmsCerebrovascular EventHemorrhagic Stroke+2 more
Evaluating Premedication Regimens (Methylprednisolone vs Dexamethasone-based) for the Prevention of Systemic and Injection Site Reactions to Motixafortide in Patients With Multiple Myeloma Undergoing Stem Cell Mobilization, PARADE Trial
Started Sep 2025
94 enrolled
Multiple Myeloma
The Effect of Methylprednisolone on the Reversal Time of Rocuronium by Sugammadex in the Pediatric Patient Group
Started Oct 2024
Depo-Medrol on Psoas After LLIF
Started May 2023
80 enrolled
Muscle WeaknessPain, PostoperativeParesthesia+1 more
Rapamycin Plus Methylprednisolone Versus Methylprednisolone Alone in Active, Moderate-to-severe Graves' Orbitopathy.
Started Sep 2022
140 enrolled
Graves Ophthalmopathy
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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.