FENOFIBRATE · IMPAX LABS
Fenofibrate tablet USP is a peroxisome proliferator-activated receptor (PPAR) alpha agonist indicated as an adjunct to diet: To reduce elevated LDL-C, Total-C, TG and Apo B, and to increase HDL-C in adult patients with primary hypercholesterolemia or mixed dyslipidemia . For treatment of adult patients with severe hypertriglyceridemia . Limitations of Use: Fenofibrate was not shown to reduce coronary heart disease morbidity and mortality in patients with type 2 diabetes mellitus .
Details
- Status
- Prescription
- First Approved
- 1993-12-31
- Routes
- ORAL
- Dosage Forms
- TABLET
Companies
FENOFIBRATE Approval History
What FENOFIBRATE Treats
31 FDA approvalsOriginally approved for its first indication in 2005 . Covers 31 distinct patient populations.
- Other (31)
Other
(31 approvals)- • Approved indication (May 2005)
- • Approved indication (Oct 2005)Letter
- • Approved indication (Dec 2005)
- • Approved indication (Mar 2008)
- • Approved indication (Dec 2011)Letter
- • Approved indication (Apr 2012)
- • Approved indication (Dec 2012)
- • Approved indication (Aug 2015)
- • Approved indication (May 2016)
- • Approved indication (Jun 2016)Label Letter
- • Approved indication (Jul 2016)
- • Approved indication (Dec 2016)
- • Approved indication (Sep 2017)
- • Approved indication (Dec 2017)
- • Approved indication (Feb 2018)
- • Approved indication (Mar 2018)
- • Approved indication (Jul 2018)
- • Approved indication (Aug 2018)
- • Approved indication (Aug 2018)
- • Approved indication (Feb 2019)
- • Approved indication (Aug 2019)
- • Approved indication (Sep 2019)
- • Approved indication (Jan 2020)
- • Approved indication (Mar 2020)
- • Approved indication (Jun 2020)
- • Approved indication (Feb 2021)
- • Approved indication (Sep 2022)
- • Approved indication (Sep 2023)
- • Approved indication (Apr 2024)
- • Approved indication (Nov 2024)
- • Approved indication (Jan 2026) New
Clinical Trial Registry
48 trials| Trial | Sponsor ID | Phase | Status | Title |
|---|---|---|---|---|
| NCT07572552 | 36265MD41030/1/26 | Ph 2 | not yet recruiting | Clinical Study Evaluating the Efficacy and Safety of Fenofibrates Versus Silymarin in Adult Patients With Sepsis |
| NCT04929379 PERL-FENO | STUDY00000156 | Ph 2 | active not recruiting | A Pilot Study of Fenofibrate to Prevent Kidney Function Loss in Type 1 Diabetes |
| NCT01320345 FAME 1 EYE | FAME0001 ACTRN12611000249954 | Ph 3 | active not recruiting | The Fenofibrate And Microvascular Events in Type 1 Diabetes Eye. |
| NCT06174402 | KY-20232219-C-1 | Ph 2, Ph 3 | active not recruiting | Fenofibrate in Combination With Ursodeoxycholic Acid in Primary Biliary Cholangitis |
| NCT06755151 | KY20232219-C-1-1 | Ph 3 | recruiting | Fenofibrate in Primary Biliary Cholangitis: a Real World Study |
| NCT07296458 | KY-20252505 | Ph 3 | recruiting | FIREFLY Trial: Fenofibrate Intervention---Randomized Evaluation in First-Line PBC Therapy |
| NCT04661358 Protocol AF | DRCR.net Protocol AF U10EY014231 | Ph 3 | active not recruiting | Fenofibrate for Prevention of DR Worsening |
| NCT05514119 FICsDCD results posted | 22-007122 | Ph 2 | terminated | A Study to Assess the Role of Fenofibrate in Preventing Ischemic Cholangiopathy After Liver Transplantation |
| NCT06191133 | CASE3822 | Ph 1 | recruiting | Fenofibrate in Patients With Cervical Intraepithelial Neoplasia and Invasive Cervical Carcinoma |
| NCT06155331 | Breast cancer and fenofibrate | Ph 2 | completed | Evaluation of Possible Safety and Efficacy of Fenofibrate in the Prophylaxis of Doxorubicin Induced Cardiotoxicity in Breast Cancer Patients |
| NCT06365424 | KY20151230-5-1 | Ph 2, Ph 3 | recruiting | Fenofibrate in Patients With Primary Biliary Cholangitis (PBC) |
| NCT05781698 | 1-2023 | Ph 2 | completed | Repurposing Fenofibrate in Modulating mTOR/NLRP3 Inflammasome in Patients With Ulcerative Colitis |
| NCT06623539 | jRCTs031200280 | Ph 2 | active not recruiting | Efficacy and Safety of Pemafibrate for Nonalcoholic Fatty Liver Disease |
| NCT06451900 | prophylactic fenofibrate | Ph 4 | completed | Role of Fenofibrate in Neonatal Jaundice |
| NCT03615534 results posted | 1 Al-KindyCM | Ph 4 | completed | Extended Release Niacin and Fenofibrate for the Treatment of Atherogenic Dyslipidemia in Obese Females |
| NCT03829514 results posted | Pro00079289 | Ph 4 | completed | Fenofibrate in Type 2 Diabetes |
| NCT03515213 results posted | 20163022 | Ph 2 | completed | Safety and Efficacy of Fenofibrate as a Treatment for Huntington's Disease |
| NCT03510884 results posted | EFC14643 2017-001903-60, U1111-1193-0721 | Ph 3 | completed | An Efficacy and Safety Study of Alirocumab in Children and Adolescents With Heterozygous Familial Hypercholesterolemia |
| NCT02823353 | KY20151230-4 | Ph 3 | completed | Fenofibrate in Combination With Ursodeoxycholic Acid in Primary Biliary Cirrhosis |
| NCT03001817 results posted | K-877-301 | Ph 3 | completed | Study to Evaluate the Efficacy and Safety of K-877 in Adult Patients With Fasting High Triglyceride Levels and Normal Renal Function |
| NCT03011450 results posted | K-877-303 | Ph 3 | completed | Study to Evaluate the Efficacy and Safety of K-877 in Adult Patients With Fasting High Triglyceride Levels and Mild or Moderate Renal Impairment |
| NCT02965911 | BJ302-FGRXGB-002 | Ph 1, Ph 2 | withdrawn | Efficacy and Safety of Fenofibrate Combined With UDCA in PBC Patients With an Incomplete Biochemical Response to UDCA |
| NCT03510715 results posted | EFC14660 2017-002297-39, U1111-1200-2046 | Ph 3 | completed | An Efficacy and Safety Study of Alirocumab in Children and Adolescents With Homozygous Familial Hypercholesterolemia |
| NCT02891408 HI results posted | GS-US-426-3988 | Ph 1 | completed | Study to Evaluate the Pharmacokinetics of Firsocostat or Fenofibrate in Adults With Normal and Impaired Hepatic Function |
| NCT01594983 | CLCQ908C2201 2012-000872-40 | Ph 2 | completed | A Pilot Study to Assess the Efficacy and Safety of LCQ908 Alone and in Combination With Fenofibrate or Lovaza® in Patients With Severe Hypertriglyceridemia |
| NCT01148004 | 100124 10-CC-0124 | Ph 1 | completed | The Influence of Ritonavir, Alone and in Combination With Lopinavir, on Fenofibric Acid Pharmacokinetics in Healthy Volunteers |
| NCT02452255 | 14-0441 NIH RO1GM056687 | Ph 2, Ph 3 | terminated | Fenofibrate and Propranolol in Burn Patients |
| NCT01574131 | 11-106 | Ph 4 | terminated | Acute and Long-Term Outcome Investigations of Fenofibrate on Severely Burned Patients |
| NCT02984982 ODYSSEY J-IVUS results posted | ALIROL08069 U1111-1184-8764 | Ph 4 | completed | Evaluation of Effect of Alirocumab on Coronary Atheroma Volume in Japanese Patients Hospitalized for Acute Coronary Syndrome With Hypercholesterolemia |
| NCT02890992 ODYSSEY KIDS results posted | DFI14223 2015-003766-85, U1111-1178-4764 | Ph 2 | completed | An 8-Week Dose-Finding Study to Evaluate the Efficacy and Safety of Alirocumab in Children and Adolescents With Heterozygous Familial Hypercholesterolemia |
| NCT02455336 results posted | B1925-P | Ph 2, Ph 3 | completed | Fenofibrate Treatment in SCI |
| NCT02262143 | ID-ROFE-301 | Ph 3 | completed | Phase III Study of Rosuvastatin and Fenofibrate Versus Rosuvastatin in Mixed Dyslipidemia |
| NCT02642159 results posted | LPS14354 2015-001934-19, U1111-1172-5262 | Ph 4 | completed | Efficacy and Safety of Alirocumab Versus Usual Care on Top of Maximally Tolerated Statin Therapy in Patients With Type 2 Diabetes and Mixed Dyslipidemia (ODYSSEY DM-Dyslipidemia) |
| NCT01142323 results posted | 20100533 | Ph 1, Ph 2 | terminated | Pilot Study of Fenofibrate for PSC |
| NCT02066207 | 146DDI13024 | Ph 1 | completed | CKD-337 Drug Interaction Study |
| NCT01965834 results posted | 20110069 | Ph 2 | terminated | Phase II Study to Evaluate Fenofibrate Therapy in Patients With Smoldering or Symptomatic Multiple Myeloma |
| NCT01723735 | PKD12910 U1111-1131-3203, 2012-003049-13 | Ph 1 | completed | Effect of Alirocumab (SAR236553/REGN727) Administered on Top of Ezetimibe or Fenofibrate on Lipid Profiles in Healthy Subjects |
| NCT02886299 | CL (746) | Ph 4 | completed | Randomized Comparative Efficacy and Safety Study of Intermittent Simvastatin and Fenofibrate in Hemodialysis |
| NCT01426438 results posted | ACTG A5293 1U01AI068636 | Ph 2 | completed | Endothelial Function, Lipoproteins, and Inflammation With Low HDL Cholesterol in HIV: ER Niacin Versus Fenofibrate |
| NCT01462877 results posted | W13-254 | Ph 4 | completed | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients With Dyslipidemic |
| NCT01666041 | GMC-201202 | Ph 4 | completed | Vascular and Metabolic Effects of Fenofibrate/Omega vs Fenofibrate |
| NCT02153879 LOWHDL | IISPV-HUSJR-LOWHDL | Ph 4 | completed | Characterization of High Density Lipoprotein (HDL) in Type 2 Diabetes (T2D) After Fenofibrate or Niacin Treatment |
| NCT00819910 RAFAEL results posted | C.2007.122 | Ph 4 | terminated | Rosiglitazone And Fenofibrate Additive Effects on Lipids (RAFAEL) |
| NCT01141296 | Feno-01 | Ph 2 | withdrawn | Fenofibrate in Combination With Ursodeoxycholic Acid (UDCA) in Primary Biliary Cirrhosis |
| NCT01539616 | ZYH7.10.001.01 CTRI/2011/11/002147 | Ph 2 | completed | A Clinical Trial to Evaluate the Safety and Efficacy of ZYH7 Compared to Fenofibrate in Patients With Dyslipidemia |
| NCT00872599 results posted | PPAR Alpha Agonist Grant# DK38226-21 | Ph 4 | completed | The Effect of a Peroxisome Proliferator-activated Receptor (PPAR) Alpha Agonist on Cytochrome P450 (CYP) Monooxygenase Activity in Humans |
| NCT00732485 | 07-389 SHC 08-GAL-006 | Ph 2, Ph 3 | withdrawn | Mitochondrial Oxidation and Insulin Resistance in Burn Patients Treated With Fenofibrate |
| NCT01109758 | S282.1.002 2007-006147-52 | Ph 1 | completed | Effects of Fenofibrate on Gene Expression in Healthy Volunteers |
Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
FENOFIBRATE FDA Label Details
Indications & Usage
FDA Label (PDF)Fenofibrate tablet USP is a peroxisome proliferator-activated receptor (PPAR) alpha agonist indicated as an adjunct to diet: To reduce elevated LDL-C, Total-C, TG and Apo B, and to increase HDL-C in adult patients with primary hypercholesterolemia or mixed dyslipidemia . For treatment of adult patients with severe hypertriglyceridemia . Limitations of Use: Fenofibrate was not shown to reduce coronary heart disease morbidity and mortality in patients with type 2 diabetes mellitus . 1.1 Primary Hypercholesterolemia or Mixed Dyslipidemia Fenofibrate tablet USP is indicated as adjunctive therapy t...
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.