NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
JRCT ID: jRCT2031210371

Registered date:08/10/2021

A Phase 2a Study Assessing the Efficacy and Safety of STN1010905 Ophthalmic Suspension in Subjects with MGD

Basic Information

Recruitment status Complete
Health condition(s) or Problem(s) studiedMGD (Meibomian Gland Dysfunction)
Date of first enrollment18/10/2021
Target sample size36
Countries of recruitment
Study typeInterventional
Intervention(s)Screening period : Artificial tear (BID, Both eyes) Treatment period : STN1010905 ophthalmic suspension or Placebo (BID, Both eyes)

Outcome(s)

Primary OutcomeSign of Meibomian glands
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum>= 20age old
Age maximumNot applicable
GenderBoth
Include criteriaOutpatient Diagnosed as MGD Having ocular symptoms
Exclude criteriaOcular disease which needs treatment expect MGD and DRYEYE Requires contact lenses wear during the study Any decision by the Investigator to terminate a subject in screening

Related Information

Contact

Public contact
Name Yukie Migita
Address 4-20 Ofuka-cho, Kita-ku, Osaka, Japan Osaka Japan 530-8552
Telephone +81-6-4802-9341
E-mail clinical@santen.co.jp
Affiliation Santen pharmaceutical co.,ltd
Scientific contact
Name Yukie Migita
Address 4-20 Ofuka-cho, Kita-ku, Osaka, Japan Osaka Japan 530-8552
Telephone +81-6-4802-9341
E-mail clinical@santen.co.jp
Affiliation Santen pharmaceutical co.,ltd