NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
JRCT ID: jRCT2051220050

Registered date:16/06/2022

Phase 3b Study of STN1011402 ophthalmic cream in Patients With Allergic Conjunctivitis

Basic Information

Recruitment status Complete
Health condition(s) or Problem(s) studiedAllergic Conjunctivitis
Date of first enrollment25/06/2022
Target sample size50
Countries of recruitment
Study typeInterventional
Intervention(s)0.5% STN1011402 ophthalmic cream (approximately 30mg/time, once a day) and 0.1% Epinastine hydrochloride ophthalmic solution (1 drop/time, twice a day) will be applied for 2 weeks at a time.

Outcome(s)

Primary OutcomeUsability and burden of use (Questionnaire)
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum>= 20age old
Age maximumNot applicable
GenderBoth
Include criteriaProvided signed, written informed consent. Has a positive result from a Type I allergy test.
Exclude criteriaEye disease other than allergic conjunctivitis is present and requires treatment. Females who are pregnant, nursing or planning a pregnancy, or females of childbearing potential who are not using a reliable method of contraception.

Related Information

Contact

Public contact
Name Sakamoto Kayoko
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 Sakamoto Kayoko
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