Recruiting

Secukinumab

Sponsor:

Novartis Pharmaceuticals

Code:

NCT07282015

Conditions

Hidradenitis Suppurativa

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

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.

Conditions

Hidradenitis Suppurativa

Study ID

NCT07282015

Start date

Dec 12, 2025

Status verified date

Jun, 2026

Completion date

Feb 11, 2028

Anticipated

Primary completion date

Feb 11, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Patients must give written, signed, and dated informed consent before any information is collected and any study-related activity is performed.
2. Adult patients at the time of informed consent signature.
3. Patients with the diagnosis of moderate-to-severe HS, as determined by the dermatologist.
4. 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.
5. Patients who can understand written and spoken Canadian English or French.

Exclusion Criteria:

1. Any medical or psychological condition in the treating physician's opinion that may prevent the patient from study participation.
2. Patients who have any contraindications to treatment with secukinumab, as defined in the Canadian PM.
3. Patients who have had any prior exposure to secukinumab (i.e., >7 days prior to the baseline visit).

Study Design

Enrollment

142 participants

Anticipated

Interventions and Outcome Measures

Arms

Secukinumab

Patients with moderate-to-severe HS who are prescribed secukinumab in Canadian routine clinical practice

Primary outcome measure

  • Proportion of patients who experience a change in disease severity classification [ Time Frame: Baseline, month 12 ]

Central Contacts and Locations

Central contacts

Novartis Pharmaceuticals

novartis.email@novartis.com

Locations

Novartis Investigative Site

Recruiting

Calgary, Alberta, Canada, T2J 7E1

Novartis Investigative Site

Recruiting

Calgary, Alberta, Canada, T3E 0B2

Novartis Investigative Site

Recruiting

Winnipeg, Manitoba, Canada, R3M 3Z4

Novartis Investigative Site

Recruiting

Fredericton, New Brunswick, Canada, E3B 1G9

Novartis Investigative Site

Recruiting

St. John's, Newfoundland and Labrador, Canada, A1E 1V4

Novartis Investigative Site

Recruiting

Cobourg, Ontario, Canada, K9A 4J9

Novartis Investigative Site

Recruiting

Hamilton, Ontario, Canada, L8P4B4

Novartis Investigative Site

Recruiting

London, Ontario, Canada, N6H 5L5

Novartis Investigative Site

Recruiting

Markham, Ontario, Canada, L3P 1X3

Novartis Investigative Site

Recruiting

Mississauga, Ontario, Canada, L4W 0C2

Novartis Investigative Site

Recruiting

Richmond Hill, Ontario, Canada, L4C 9M7

Novartis Investigative Site

Recruiting

Toronto, Ontario, Canada, M4E 1R7

Novartis Investigative Site

Recruiting

Saint-Jérôme, Quebec, Canada, J7Z 7E2

Novartis Investigative Site

Recruiting

Sherbrooke, Quebec, Canada, J1L 0H8

Novartis Investigative Site

Recruiting

Saskatoon, Saskatchewan, Canada, S7N0N5

More Information

Sponsor

Novartis Pharmaceuticals

Last update posted

Jun 23, 2026

Last verified

Jun, 2026

Keywords

  • Hidradenitis Suppurativa
  • NIS
  • secukinumab
  • Phase IV

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Novartis Pharmaceuticals on 2026-06-23.