Study CSL324\_1002 will investigate the safety and pharmacokinetics of repeat doses of CSL324 in subjects with hidradenitis suppurativa and palmoplantar pustulosis. CSL324 is a novel, recombinant therapy that may treat diseases caused by increased numbers of neutrophils at sites of inflammation.
Age range
18 Years – 75 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Incidence of treatment-emergent adverse events (TEAEs)
Timeframe: Up to 24 weeks
TEAEs by severity
Timeframe: Up to 24 weeks
TEAEs by casuality
Timeframe: Up to 24 weeks
Incidence of adverse events of special interest (AESIs): Grade 3 and 4 neutropenia
Timeframe: Up to 24 weeks
AESIs: Grade 3 and 4 neutropenia by causality
Timeframe: Up to 24 weeks
Incidence of AESIs: Grade 3 and 4 infection
Timeframe: Up to 24 weeks
AESIs: Grade 3 and 4 infection by causality
Timeframe: Up to 24 weeks