Short-term treatment satisfaction with Cosentyx for hidradenitis suppurativa in Saudi Arabia

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a 24-week, single-arm, prospective observational study of adults with moderate-to-severe hidradenitis suppurativa treated in routine clinical practice in Saudi Arabia. Secukinumab-naive patients who begin Cosentyx will have data collected at baseline and at 24 weeks from electronic medical records and patient-reported questionnaires (TSQM, DLQI, and NPRS-11). The primary focus is patient-reported treatment satisfaction (convenience, perceived safety, perceived effectiveness, and global satisfaction) measured by the TSQM at week 24. The design follows standard-of-care visits and allows concurrent antibiotics or surgery as clinically indicated.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Male or Female adult patients ≥18 years of age at the time of data collection.
2. Patient with a confirmed diagnosis of active moderate to severe HS.
3. Secukinumab naive patients (first dose to coincide within one month of the signature of the informed consent) as per locally approved label.
4. Patients can be using antibiotics or have undergone surgery as per routine clinical practice.
5. Patients agree to sign an informed consent form (ICF) to be able to complete the questionnaires.

Exclusion Criteria:

1. Patients not fulfilling any of the above-mentioned inclusion criteria.
2. Patient's refusal to be included in the study or refusal to sign the ICF.
3. A history of off-label indication uses of biological treatment or JAK inhibitor.

Where it's running

• Novartis Investigative Site
  Riyadh, Sau, Saudi Arabia Recruiting
• Novartis Investigative Site
  Jeddah, Saudi Arabia Recruiting
• Novartis Investigative Site
  Jeddah, Saudi Arabia Recruiting
• Novartis Investigative Site
  Riyadh, Saudi Arabia Recruiting

Study contacts

• Study coordinator: Novartis Pharmaceuticals
• Email: novartis.email@novartis.com
• Phone: +41613241111

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Secukinumab in Chinese adults with moderate to severe hidradenitis suppurativa

  This trial tests two dosing regimens of secukinumab to see if they can help Chinese adults with moderate to severe hidradenitis suppurativa.

  Recruiting at 10 sites Phase 4 Novartis · Guangzhou, Guangdong and 9 other locations · NCT07489573

• Secukinumab for moderate-to-severe hidradenitis suppurativa

  This study tests whether secukinumab helps adults with moderate-to-severe hidradenitis suppurativa who have not improved with antibiotics, isotretinoin, or TNF inhibitors.

  Recruiting Peking Union Medical College · Beijing, Beijing Municipality · NCT07109765

• Evaluating secukinumab's effectiveness with surgery for hidradenitis suppurativa

  This study is testing if using secukinumab along with surgery can help people with moderate to severe hidradenitis suppurativa feel better and have fewer problems after surgery.

  Recruiting Peking Union Medical College · Nanjing, Jiangsu · NCT06926192

• Soquelitinib in adults with hidradenitis suppurativa

  This study tests whether oral soquelitinib can help adults with moderate-to-severe hidradenitis suppurativa.

  Recruiting at 9 sites Phase 1 Corvus Pharmaceuticals, Inc. · West Lafayette, Indiana and 10 other locations · NCT07828860

• ORKA-002 versus placebo for moderate-to-severe hidradenitis suppurativa

  A study tests ORKA-002 against placebo in adults with moderate-to-severe hidradenitis suppurativa to see if it helps reduce symptoms.

  Recruiting at 25 sites Phase 2 Oruka Therapeutics, Inc. · Birmingham, Alabama and 24 other locations · NCT07783542

• SPY072 in adults with moderate to severe hidradenitis suppurativa

  This study tests whether SPY072 can help adults with moderate to severe hidradenitis suppurativa when added to their current care, compared with a placebo over 16 weeks.

  Recruiting at 7 sites Phase 2 Spyre Therapeutics, Inc. · Birmingham, Alabama and 33 other locations · NCT07766005

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.