POC Study to Evaluate the Efficacy and Safety of ESK-001 in Patients With Active Intermediate, Posterior, or Pan NIU

PHASE2TerminatedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

June 14, 2023

Primary Completion Date

August 13, 2024

Study Completion Date

August 13, 2024

Conditions
Uveitis Posterior Non-InfectiousUveitis, IntermediateNoninfectious Panuveitis
Interventions
DRUG

ESK-001

Oral tablet

Trial Locations (17)

16507

Investigator Site #1064, Erie

21740

Investigator Site #1085, Hagerstown

27705

Investigator Site #1083, Durham

37203

Investigator Site#1066, Nashville

37232

Investigator Site #1084, Nashville

60304

Investigator Site #1086, Oak Park

75075

Investigator Site #1078, Plano

77401

Investigator Site#1075, Bellaire

77494

Investigator Site #1074, Katy

80228

Investigator Site#1068, Lakewood

90033

Investigator Site #1073, Los Angeles

90095

Investigator Site #1072, Los Angeles

90211

Investigator Site#1065, Beverly Hills

94303

Investigator Site #1080, Palo Alto

95825

Investigator Site #1079, Sacramento

02451

Investigator Site #1069, Waltham

07650

Investigator Site #1076, Palisades Park

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Alumis Inc

INDUSTRY

NCT05953688 - POC Study to Evaluate the Efficacy and Safety of ESK-001 in Patients With Active Intermediate, Posterior, or Pan NIU | Biotech Hunter | Biotech Hunter