MedPath

Kowa Research Institute, Inc.

πŸ‡ΊπŸ‡ΈUnited States
Ownership
Subsidiary
Established
1981-01-01
Employees
1
Market Cap
-
Website
http://www.kowaus.com

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
2025-05-09
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
17
Registration Number
NCT06525311
Locations
πŸ‡―πŸ‡΅

301, Yufu, Japan

πŸ‡ΊπŸ‡Έ

Arizona Liver Health, Chandler, Arizona, United States

πŸ‡ΊπŸ‡Έ

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

and more 11 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
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
2025-02-26
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
45
Registration Number
NCT06247735
Locations
πŸ‡ΊπŸ‡Έ

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

πŸ‡ΊπŸ‡Έ

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

πŸ‡ΊπŸ‡Έ

Velocity Clinical Research, Santa Ana, 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
2025-03-03
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
110
Registration Number
NCT05826353
Locations
πŸ‡ΊπŸ‡Έ

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

πŸ‡ΊπŸ‡Έ

Macy Eye Center, Los Angeles, California, United States

πŸ‡ΊπŸ‡Έ

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
2025-03-03
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
107
Registration Number
NCT05795699
Locations
πŸ‡ΊπŸ‡Έ

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

πŸ‡ΊπŸ‡Έ

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

πŸ‡ΊπŸ‡Έ

Sacramento Eye Consultants, Sacramento, California, United States

and more 44 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
πŸ‡ΊπŸ‡Έ

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

A Study to Investigate the Safety and Efficacy of Ripasudil (K-321) Eye Drops After Cataract Surgery

Phase 3
Completed
Conditions
Corneal Edema After Cataract Surgery
Interventions
Drug: Placebo
First Posted Date
2022-09-06
Last Posted Date
2024-05-24
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
331
Registration Number
NCT05528172
Locations
πŸ‡ΊπŸ‡Έ

Eye Care Specialists, Kingston, Pennsylvania, United States

πŸ‡ΊπŸ‡Έ

Center for Sight, Las Vegas, Nevada, United States

πŸ‡ΊπŸ‡Έ

Houston Eye Associates, Houston, Texas, United States

and more 41 locations

A Study to Confirm the Efficacy and Safety of K-161 Ophthalmic Solution for Treatment of Moderate to Severe Dry Eye Disease

Phase 3
Completed
Conditions
Dry Eye Disease
Interventions
Drug: Placebo
First Posted Date
2022-06-03
Last Posted Date
2025-01-14
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
644
Registration Number
NCT05403827
Locations
πŸ‡ΊπŸ‡Έ

Trinity Research Group, Dothan, Alabama, United States

πŸ‡ΊπŸ‡Έ

Orange County Ophthalmology Medical Group, Garden Grove, California, United States

πŸ‡ΊπŸ‡Έ

LoBue Laser and Eye Medical Center, Murrieta, California, United States

and more 47 locations

Study to Evaluate the Efficacy and Safety of K-877-ER and CSG452 in Participants With NASH With Liver Fibrosis

Phase 2
Recruiting
Conditions
NASH
Interventions
First Posted Date
2022-04-14
Last Posted Date
2025-05-15
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
200
Registration Number
NCT05327127
Locations
πŸ‡ΊπŸ‡Έ

Centricity Research, Columbus, Georgia, United States

πŸ‡ΊπŸ‡Έ

Birmingham Digestive Health Research, Inc., Birmingham, Alabama, United States

πŸ‡ΊπŸ‡Έ

Adobe Clinical Research, LLC, Tucson, Arizona, United States

and more 98 locations

Study to Assess the Food Effect of K-877 in Healthy Adult Volunteers

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2021-02-08
Last Posted Date
2021-08-09
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
18
Registration Number
NCT04742218
Locations
πŸ‡ΊπŸ‡Έ

PPD Development, LP, Austin, Texas, United States

A Study to Evaluate the Efficacy and Safety of K-285 Compared With Menthol Gel for the Treatment of Delayed Onset Muscle Soreness (DOMS) in the Lower Extremity

Phase 2
Terminated
Conditions
Acute Pain
Interventions
First Posted Date
2020-07-23
Last Posted Date
2024-12-27
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
126
Registration Number
NCT04484428
Locations
πŸ‡ΊπŸ‡Έ

Lotus Clinical Research, LLC, Pasadena, California, United States

Β© Copyright 2025. All Rights Reserved by MedPath