Long-term treatment of hidradenitis suppurativa with secukinumab
Résumé de l'étude
This study is an extension study of the main studies CAIN457M2301 and CAIN457M2302. Both studies were also conducted at Swiss centers. Eligible patients are those who completed the entire study treatment phase (52 weeks) in one of the main studies. This study examines the safety, tolerability, and efficacy of further administration of secukinumab for up to 4 years in individuals affected by hidradenitis suppurativa (HS). Secukinumab is a medication that is a monoclonal antibody. Secukinumab binds to and reduces the activity of a cytokine (a messenger in the body) called interleukin-17A (IL-17A). IL-17A is believed to be partially responsible for the inflammation in HS (pain, swelling, and redness) and that IL-17A contributes to HS symptoms. A medication that acts on IL-17A could therefore help alleviate these symptoms. Secukinumab is a medication that is not approved by the Swiss Agency for Therapeutic Products Swissmedic for the treatment of patients with HS, but it has been approved for the treatment of individuals with other conditions (psoriasis, psoriatic arthritis, ankylosing spondylitis) and is marketed under the name Cosentyx. Patients are randomly assigned to one of two treatment groups 1) The same dose of secukinumab as in the previous study (66% probability) or 2) Placebo (33% probability). If placebo is assigned and symptoms worsen, the placebo is discontinued and there is the possibility to start an open-label treatment with secukinumab. After a maximum period of 1 year, each participant has the opportunity to continue with an open-label secukinumab treatment for up to an additional 3 years, administered every 2 or 4 weeks.
(BASEC)
Intervention étudiée
When a patient has completed the entire study treatment phase (52 weeks) of one of the main studies and agrees to participate in this study, the participant is randomly assigned to one of the 2 following treatment groups: - Secukinumab 300 mg every 2 weeks or every 4 weeks (the same dose as in the previous study is continued) - Placebo group for secukinumab treatment with 300 mg every 2 weeks or every 4 weeks. The study medication is provided in 2 ml pre-filled syringes and is injected under the skin. Participants are expected to self-administer the study treatment (inject), if possible. Participation in the study may last a total of 4 years.
(BASEC)
Maladie en cours d'investigation
This study examines patients with hidradenitis suppurativa (HS). HS is a chronic inflammatory skin disease in which lumps form under the skin in areas where skin rubs against skin, which can lead to inflammatory pain, fluid drainage, scarring, and potentially even reduced mobility of the arms and legs.
(BASEC)
Individuals who have completed the entire study treatment phase (52 weeks) of one of the main studies (CAIN457M2301 or CAIN457M2302) may participate. (BASEC)
Critères d'exclusion
Individuals who do not practice adequate contraception, as well as pregnant and breastfeeding women, may not participate. Additionally, individuals who would take certain medications in parallel with the study that are not allowed are also excluded. Further information can be obtained from the study physician. (BASEC)
Lieu de l’étude
Berne, Genève, Lausanne
(BASEC)
Sponsor
Novartis Pharma Schweiz AG
(BASEC)
Contact pour plus d'informations sur l'étude
Personne de contact en Suisse
Kerstin Wanke
+41793308956
kerstin.wanke@clutternovartis.comNovartis Pharma Schweiz AG
(BASEC)
Informations générales
Novartis Pharmaceuticals
(ICTRP)
Informations scientifiques
Novartis Pharmaceuticals
(ICTRP)
Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)
Commission cantonale d'éthique de Genève
(BASEC)
Date d'approbation du comité d'éthique
08.06.2020
(BASEC)
Identifiant de l'essai ICTRP
NCT04179175 (ICTRP)
Titre officiel (approuvé par le comité d'éthique)
A multicenter, double-blind, randomized withdrawal extension study of subcutaneous secukinumab to demonstrate long-term efficacy, safety and tolerability in subjects with moderate to severe hidradenitis suppurativa (BASEC)
Titre académique
A Multicenter, Double-blind, Randomized Withdrawal Extension Study of Subcutaneous Secukinumab to Demonstrate Long-term Efficacy, Safety and Tolerability in Subjects With Moderate to Severe Hidradenitis Suppurativa (ICTRP)
Titre public
Extension Study to Assess Effects of Non-interrupted Versus Interrupted and Long Term Treatment of Two Dose Regimes of Secukinumab in Subjects With Hidradenitis Suppurativa (ICTRP)
Maladie en cours d'investigation
Hidradenitis Suppurativa (ICTRP)
Intervention étudiée
Drug: secukinumabDrug: secukinumab (ICTRP)
Type d'essai
Interventional (ICTRP)
Plan de l'étude
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Triple (Participant, Care Provider, Investigator). (ICTRP)
Critères d'inclusion/exclusion
Inclusion Criteria:
- written informed consent must be obtained before any assessment is performed
- subject must have completed the study treatment period (52 weeks) in the core
studies (AIN457M2301 or AIN457M2302) and had received secukinumab treatment during
Treatment Period 2
Exclusion Criteria:
- protocol deviation in the core study which will prevent the meaningful analysis of
the extension study
- ongoing or planned use of prohibited HS or non-HS treatment
- participation in the extension could expose the subject to an undue safety risk
- current sever progressive or uncontrolled disease which renders the subject
unsuitable for the study (ICTRP)
non disponible
Critères d'évaluation principaux et secondaires
Time to Loss of Response (LOR) up to Week 104 in Hidradenitis Suppurativa Clinical Response (HiSCR) Responders;Incidence Rate of Participants Achieving Loss of Response (LOR) up to Week 104 in Hidradenitis Suppurativa Clinical Response (HiSCR) Responders (ICTRP)
Number of Participants With Treatment Emergent Adverse Events (ICTRP)
Date d'enregistrement
25.11.2019 (ICTRP)
Inclusion du premier participant
non disponible
Sponsors secondaires
non disponible
Contacts supplémentaires
Novartis Pharmaceuticals, Novartis Pharmaceuticals (ICTRP)
ID secondaires
2023-508956-20, CAIN457M2301E1 (ICTRP)
Résultats-Données individuelles des participants
non disponible
Informations complémentaires sur l'essai
https://clinicaltrials.gov/study/NCT04179175 (ICTRP)
Résultats de l'essai
Résumé des résultats
non disponible
Lien vers les résultats dans le registre primaire
non disponible