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Pemafibrate

Alternative Names: pemafibrate, K-877, K877, K 877
Latest Update: 2024-12-14
Latest Update Note: Clinical Trial Update

Product Description

Kowa is developing Pemafibrate as a treatment for Type 2 Diabetes and Dyslipidemia. (Sourced from: https://clinicaltrials.gov/study/NCT03071692)

Mechanisms of Action: PPAR-a Agonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Japan | Malaysia

Approved Indications: None

Known Adverse Events: None

Company: Kowa
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Pemafibrate

Countries in Clinic: Argentina, Brazil, Bulgaria, Canada, China, Japan, Spain, United States

Active Clinical Trial Count: 16

Highest Development Phases

Phase 3: Dyslipidemia|Hypercholesterolemia|Ischemic Stroke|Myocardial Infarction|Type 2 Diabetes

Phase 2: Biliary Cirrhosis|Cholangitis|Hepatitis, Alcoholic|Liver Cirrhosis|Non-alcoholic Steatohepatitis

Phase 1: Healthy Volunteers|Hyperlipidemia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

K-001-201

P2

Unknown Status

Liver Cirrhosis|Non-alcoholic Steatohepatitis|Hepatitis, Alcoholic

2026-07-31

2021-003901-23

P2

Active, not recruiting

Liver Cirrhosis|Non-alcoholic Steatohepatitis|Hepatitis, Alcoholic

2026-05-04

jRCT2071230106

P2

Recruiting

Cholangitis|Biliary Cirrhosis

2026-04-08

K-001-201

P2

Recruiting

Liver Cirrhosis|Non-alcoholic Steatohepatitis

2026-02-01

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