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Kowa Research Institute, Inc.

🇺🇸United States
Ownership
Subsidiary
Established
1981-01-01
Employees
1
Market Cap
-
Website
http://www.kowaus.com

Clinical Trials

74

Active:28
Completed:38

Trial Phases

5 Phases

Phase 1:42
Phase 2:10
Phase 3:13
+2 more phases

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (73 trials with phase data)• Click on a phase to view related trials

Phase 1
42 (57.5%)
Phase 3
13 (17.8%)
Phase 2
10 (13.7%)
Phase 4
7 (9.6%)
Not Applicable
1 (1.4%)

A Study to Evaluate the Pharmacokinetics and Safety of K-808 (Pemafibrate) in Subjects With Primary Biliary Cholangitis With Compensated Cirrhosis and Without Cirrhosis.

Phase 1
Completed
Conditions
Primary Biliary Cholangitis
Compensated Cirrhosis
Interventions
First Posted Date
2024-07-29
Last Posted Date
2025-05-23
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
17
Registration Number
NCT06525311
Locations
🇺🇸

Arizona Liver Health, Chandler, Arizona, United States

🇺🇸

Southern California Research Center, Inc, Coronado, California, United States

🇺🇸

Indiana University School of Medicine - Indianapolis, Indianapolis, Indiana, United States

and more 7 locations

Study to Evaluate the Efficacy and Safety of K-808 (Pemafibrate) in Participants With Primary Biliary Cholangitis (PBC) With Inadequate Response to Ursodeoxycholic Acid (UDCA) and/or Obeticholic Acid (OCA) Treatment.

Phase 2
Active, not recruiting
Conditions
Primary Biliary Cholangitis
Interventions
Drug: K-808 (Dose A)
Drug: K-808 (Dose B)
Drug: Placebo
First Posted Date
2024-02-08
Last Posted Date
2025-05-23
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
45
Registration Number
NCT06247735
Locations
🇺🇸

UA Thomas D. Boyer Liver Institute, Tucson, Arizona, United States

🇺🇸

Southern California Research Center - Coronado, Coronado, California, United States

🇺🇸

Cedars-Sinai Medical Center, Los Angeles, California, United States

and more 35 locations

A Study to Investigate the Safety and Efficacy of K-321 Eye Drops After Simultaneous Cataract Surgery and Descemetorhexis in Participants With Fuchs Endothelial Corneal Dystrophy (FECD)

Phase 3
Active, not recruiting
Conditions
Fuchs Endothelial Corneal Dystrophy
Interventions
Drug: Placebo
First Posted Date
2023-04-24
Last Posted Date
2025-06-22
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
110
Registration Number
NCT05826353
Locations
🇺🇸

Keck Hospital of USC, Los Angeles, California, United States

🇺🇸

Macy Eye Center, Los Angeles, California, United States

🇺🇸

Byers Eye Institute at Stanford, Palo Alto, California, United States

and more 40 locations

A Study to Evaluate the Safety and Efficacy of K-321 Eye Drops After Descemetorhexis in Participants With Fuchs Endothelial Corneal Dystrophy (FECD)

Phase 3
Active, not recruiting
Conditions
Fuchs Endothelial Corneal Dystrophy
Interventions
Drug: Placebo
First Posted Date
2023-04-03
Last Posted Date
2025-06-22
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
107
Registration Number
NCT05795699
Locations
🇺🇸

Keck Hospital of USC, Los Angeles, California, United States

🇺🇸

Macy Eye Center, Los Angeles, California, United States

🇺🇸

Jules Stein Eye Institute, Los Angeles, California, United States

and more 47 locations

Study to Demonstrate the Bioequivalence of Single Oral Administration of K-001 Relative to Single Oral Coadministration of Separate Tablets of K-877-ER and CSG452

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2023-02-10
Last Posted Date
2023-06-02
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
30
Registration Number
NCT05722262
Locations
🇺🇸

PPD - Austin Research Unit, Austin, Texas, United States

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