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Safety and Efficacy of STL303 In Patients With Primary Immunoglobulin A (IgA) Nephropathy
Sponsor: Sitala Bio LTD
Summary
This is a multicenter, randomized, double-blind, placebo controlled Phase IIb study to explore the efficacy and safety of STL303 capsules in IgAN patients. About 15 patients dignosed with primary IgAN will be enrolled and randomized to three cohorts and take different dosage of STL303 or placebo capsules orally according to protocol.
Official title: A Multicenter, Randomised, Double-Blinded, Placebo-Controlled Study to Evaluate the Safety and Efficacy of STL303 In Patients With Primary Immunoglobulin A (IgA) Nephropathy
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
15
Start Date
2026-08-04
Completion Date
2027-09
Last Updated
2026-09-17
Healthy Volunteers
No
Conditions
Interventions
STL303
STL303 arm participants will receive a specific dose of STL303
STL303
STL303 arm participants will receive a specific dose of STL303
Placebo capsule
Placebo arm participants will receive placebo capsules
Locations (8)
John Hunter Hospital
Newcastle, New South Wales, Australia
Nepean Hospital
Penrith, New South Wales, Australia
Prince of Wales Hospital
Sydney, New South Wales, Australia
Concord Hospital
Sydney, New South Wales, Australia
Research Site
Woolloongabba, Queensland, Australia
Research Site
Clayton, Victoria, Australia
Research Site
Saint Albans, Victoria, Australia
Royal Perth Hospital
Perth, Western Australia, Australia