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Trial + Data / Events	Status	Ph	N	Region	Interventions	Sponsor	Conditions	Primary compl	Study compl
KUS121 / KDDD
GION, NCT06178055: A Study of the Efficacy and Safety of KUS121 in Participants With Acute Non-Arteritic Central Retinal Artery Occlusion (CRAO)	Active, not recruiting	2	75	US	KUS121 high dose, KUS121 low dose, Sham procedure	Kyoto Drug Discovery and Development Co., Ltd.	Central Retinal Artery Occlusion	03/25	12/25