PhaseI/II Investigator-Initiated Trial to Investigate Safety and Efficacy of Ripasudil in Patients With Retinopathy of Prematurity

Key facts

Sponsor

Kyushu University

Principal Investigator

Mitsuru Arima, MD,PhD

Kyushu University Hospital

Intervention

Ripasudil ophthalmic solution 0.4%(drug)

Enrollment

24 target

Eligibility

All sexes

Timeline

2020 – 2022

Study locations (3)

• University Hospital of Occupational and Environmental Health, Kitakyushu, Fukuoka, Japan
• Yamaguchi University Hospital, Ube, Yamaguchi, Japan
• Kyushu University Hospital, Fukuoka, Japan

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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