ClinConnect ClinConnect Logo
Search / Trial NCT05787236

A Study of Moderate-to-severe Plaque Psoriasis Patients Response to Secukinumab Treatment in Real-world Setting

Launched by NOVARTIS PHARMACEUTICALS · Mar 15, 2023

Trial Information

Current as of June 13, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Male or female, aged at least 18 years old.
  • Diagnosed as moderate-to-severe plaque type psoriasis with PASI score ≥ 5 prior to initiating secukinumab treatment.
  • Treated with secukinumab for a minimum of 8 weeks after the initial secukinumab treatment without any interruption.
  • Patients included in this study received the initial secukinumab treatment within the period of 1 August 2017 to 31 October 2019. With the secondary endpoint of 52 weeks, the latest recorded data included in the analysis was recorded on 31 October 2020.
  • Exclusion Criteria
  • Patients with other types of psoriasis.
  • Patients with incomplete information on PASI score at Weeks 0, 8, and 16 in their medical records.

About Novartis Pharmaceuticals

Novartis Pharmaceuticals is a global healthcare company dedicated to reimagining medicine to improve and extend people's lives. With a strong focus on innovation, Novartis engages in the research, development, and commercialization of a broad range of therapies across various therapeutic areas, including oncology, cardiology, dermatology, and neuroscience. The company is committed to advancing scientific knowledge and patient care through clinical trials that prioritize safety and efficacy. Novartis leverages cutting-edge technology and collaborative partnerships to address unmet medical needs and deliver transformative treatments that enhance patient outcomes worldwide.

Locations

Jakarta, , Indonesia

Patients applied

0 patients applied

Trial Officials

Novartis Pharmaceuticals

Study Director

Novartis Pharmaceuticals

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials