Clinical trial
A Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous…
NCT01729754 · Sun Pharmaceutical Industries Limited, Industry · Completed
Key facts
| NCT number | NCT01729754 |
|---|---|
| Title | A Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222/MK-3222) in Participants With Moderate-to-Severe Chronic Plaque Psoriasis Followed by a Long-term Extension Study (MK-3222-011) |
| Official title | A 52-Week, Phase 3, Randomized, Active Comparator and Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222/MK-3222), Followed by an Optional Long-Term Safety Extension Study, in Subjects With Moderate-to-Severe Chronic… |
| Acronym | reSURFACE 2 |
| Lead sponsor | Sun Pharmaceutical Industries Limited, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Plaque Psoriasis |
| Intervention type | Drug |
| Interventions | Tildrakizumab 200 mg, Tildrakizumab 100 mg, Tildrakizumab Placebo, Etanercept Placebo, Etanercept 50 mg |
| Enrollment | 1,090 |
| Start date | Feb 5, 2013 |
| Primary completion | Sep 28, 2015 |
| Completion | Oct 26, 2021 |
| First posted | Nov 20, 2012 |
| Last update posted | Mar 8, 2022 |
At a glance
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: