Real-world Secukinumab Outcomes in Canadian HS Patients
ConditionHidradenitis Suppurativa
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorNovartis Pharmaceuticals
About this trial
The HS-RISE study aims to assess real-world HS treatment outcomes and patterns, safety of secukinumab, and to describe the baseline characteristics of patients diagnosed with moderate-to- severe HS who are prescribed secukinumab in Canadian routine clinical practice.
Eligibility criteria
Qualifiers
Patients must give written, signed, and dated informed consent before any information is collected and any study-related activity is performed.
Adult patients at the time of informed consent signature.
Patients with the diagnosis of moderate-to-severe HS, as determined by the dermatologist.
Patients who have been newly prescribed secukinumab as part of routine clinical care according to the approved Canadian PM. The decision to prescribe secukinumab must be made prior to,and independent of, study participation. First treatment with secukinumab must occur no more than 7 days (≤7 days) prior to Baseline visit.
Disqualifiers
Any medical or psychological condition in the treating physician's opinion that may prevent the patient from study participation.
Patients who have any contraindications to treatment with secukinumab, as defined in the Canadian PM.
Patients who have had any prior exposure to secukinumab (i.e., >7 days prior to the baseline visit).
Trial design
Treatments tested in this trial
- Not listed
Trial groups
142 Participants
are grouped into 1 trial groupSponsors and collaborators
Source ClinicalTrials.gov