drug · small molecule
MEDROL
Marketedupdated 5mo agoby $PFE PFIZER INC🔗 ChEMBL
Approvedcommunity read0 votes
🐶 often sniffed alongside
top 8- tagApproval454 co-mentions · 127 sources
- drugMETHYLPREDNISOLONE231 co-mentions · 131 sources
- drugSOLU-MEDROL192 co-mentions · 48 sources
- drugDEPO-MEDROL137 co-mentions · 44 sources
- drugmethylprednisolone sodium succinate96 co-mentions · 48 sources
- drugMETHYLPREDNISOLONE ACETATE75 co-mentions · 44 sources
- tagSmall Molecule58 co-mentions · 37 sources
- companyGreenstone LLC2 co-mentions · 1 sources
Small molecule drug with a maximum clinical stage of Approval (across all indications), with 17 approved and 94 investigational indications.
indications
investigational
IBD (Crohn's + UC)Rheumatoid ArthritisPsoriasisLupusAsthma
targets
Glucocorticoid receptor
all catalysts(34)
approval · 33
Oct 24, 1957
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Sep 10, 1976
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Apr 11, 1978
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Apr 5, 1979
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Apr 5, 1979
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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May 30, 1979
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Apr 14, 1980
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Oct 8, 1980
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Mar 9, 1983
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Feb 24, 1987
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Jan 5, 1989
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Jan 28, 1993
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Dec 28, 1993
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Oct 31, 1997
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Dec 5, 1997
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Jun 23, 1998
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Oct 29, 1999
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Dec 1, 1999
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Oct 12, 2001
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Oct 12, 2001
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Oct 25, 2002
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Nov 20, 2002
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Nov 20, 2002
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Jul 18, 2013
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Jul 24, 2018
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Aug 26, 2019
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Dec 19, 2023
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Jun 5, 2024
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Aug 1, 2025
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Aug 1, 2025
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Aug 1, 2025
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Nov 4, 2025
approval
$PFE28.28+1.65%
MEDROL (METHYLPREDNISOLONE) — FDA approval
MEDROL
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Apr 10, 2026
approval
METHYLPREDNISOLONE — FDA approval
MEDROL
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Trials studying MEDROL
- phase2A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Obinutuzumab in Adolescents With Active Class III or IV Lupus Nephritis and the Safety and PK of Obinutuzumab in Pediatric Participants
- phase3A Study Evaluating the Efficacy and Safety of Obinutuzumab in Participants With Primary Membranous Nephropathy
- phase3A Study to Evaluate Zilovertamab Vedotin (MK-2140) Combination With Rituximab Plus Cyclophosphamide, Doxorubicin, and Prednisone (R-CHP) Versus Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Participants With Previously Untreated DLBCL (MK-2140-010)
- phase2A Phase 1/2 Study of Intravenous Gene Transfer With an AAV9 Vector Expressing Human Beta-galactosidase in Type I and Type II GM1 Gangliosidosis
- phase3A Study to Investigate the Efficacy and Safety of Frexalimab Versus Tacrolimus in Adults Undergoing Kidney Transplantation
- phase2Phase 1/2a Clinical Trial of PR001 (LY3884961) in Patients With Parkinson's Disease With at Least One GBA1 Mutation (PROPEL)
- phase2Study of ASP2957 in Male Participants With X-linked Myotubular Myopathy Who Need Ventilators
- phase3SC Versus IV Isatuximab in Combination With Pomalidomide and Dexamethasone in RRMM
News(1)
- Opinion: The U.S. pharmaceutical supply chain problem is not about ChinaThe national security framing of the discussion around pharmaceutical supply chain vulnerabilities is a distraction, writes Pooja Yerramilli.stat · 2mo ago
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