A Clinical Study to Evaluate the Efficacy and Safety of CKD-351

  • End date
    Dec 5, 2022
  • participants needed
  • sponsor
    Chong Kun Dang Pharmaceutical
Updated on 25 January 2021
brimonidine tartrate ophthalmic solution
pigmentary glaucoma
primary open angle glaucoma


The purpose of this study is to evaluate efficacy and safety of CKD-351


Multi center, Randomized, Open-label, Active controlled, Phase 2 trial, Proof Of Concept Study to evaluate the efficacy and safety of CKD-351 in primary open angle glaucoma or ocular hypertension patients

Condition EYE DISORDER, Eye Disorders/Infections, Eye Disorders/Infections (Pediatric), Dry Eye Disease, Eye Disease, Ocular Hypertension, Ocular Hypertension, Glaucoma, Glaucoma, Pigmentary glaucoma, Open Angle Glaucoma, Eye Disorders/Infections, Dry Eye Disease, Primary Open Angle Glaucoma, Eye Disorders/Infections (Pediatric), Eye Disease, Open Angle Glaucoma
Treatment CKD-351, Latanoprost+Dorzolmamide
Clinical Study IdentifierNCT04448223
SponsorChong Kun Dang Pharmaceutical
Last Modified on25 January 2021


Yes No Not Sure

Inclusion Criteria

More than the age of 19 years old
Subjects who has primary open-angle glaucoma or ocular hypertension
Subjects who sign on an informed consent form willingly

Exclusion Criteria

Subjects with intraocular pressure 35 mmHg at Visit 1 or Visit 2 (AM 09:00)
Subjects with a maximum corrected visual acuity 0.3 in the selected evaluation eye at Visit 1 or Visit 2
Subjects who were diagnosed as below
Intraocular lens
Acute or Chronic Closed-Angle Glaucoma
Secondary Glaucoma
Subjects with ocular inflammation or infection within the last 3 months
Subjects with significant history of ocular trauma during the last 6 months or who underwent surgical opthalmic surgery
Subjects who received topical or systemic steroids within the last 1 month
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact



Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider


Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 



Reply by • Private

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note