Clinical development

Advancing CIT-013 through clinical development

Citryll has identified multiple antibodies targeting ETosis. Our lead target, CIT-013, is currently under clinical development and has started Phase 2a studies in rheumatoid arthritis (RA) and hidradenitis suppurativa (HS) in 2025.

Phase 1 - First in human studies

Q3 2022 - finalized
Single ascending dose in healthy volunteers
CIT-013 was well tolerated within therapeutic window, PK as expected.
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Q3 2022 - finalized
Q4 2022 - finalized
LPS challenge in healthy volunteers
Study showed excellent target engagement via complete suppression of LPS-induced NETs.
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Q4 2022 - finalized
Q1 2023 - finalized
Subcutaneous single dosing in healthy volunteers
CIT-013 well-tolerated, good bioavailability.
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Q1 2023 - finalized
Q3 2024 - finalized
Repeat dosing In Rheumatoid Arthritis patient volunteers
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Q3 2024 - finalized

Phase 2a

Q3 2025 - first patient dosed
Phase 2a
in Rheumatoid Arthritis
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Q3 2025 - first patient dosed
Q4 2025 - first patient dosed
Phase 2a
in Hidradenitis Suppurativa
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Q4 2025 - first patient dosed

Future development opportunities

After successful Phase 2a studies of our ET targeting approach in RA and HS, there are opportunities to expand the clinical development into other immune-mediated inflammatory diseases in which ETs play a pathogenic role.

Clinical trial opportunities for patients

Citryll is conducting clinical trials for CIT-013, an investigational therapy developed to address Rheumatoid Arthritis (RA) and Hidradenitis Suppurativa (HS). This clinical research seeks to understand CIT-013’s potential effectiveness, safety, and impact on patient quality of life. We expect two clinical trials to start by mid 2025.