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Efficacy and safety of tildrakizumab for plaque psoriasis with continuous dosing, treatment interruption, dose adjustments and switching from etanercept: results from phase III studies.
Kimball, A B; Papp, K A; Reich, K; Gooderham, M; Li, Q; Cichanowitz, N; La Rosa, C; Blauvelt, A.
Affiliation
  • Kimball AB; Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, U.S.A.
  • Papp KA; K. Papp Clinical Research and Probity Medical Research, Waterloo, ON, Canada.
  • Reich K; Translational Research in Inflammatory Skin Diseases, Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Gooderham M; Skinflammation® Center, Hamburg, Germany.
  • Li Q; Skin Centre for Dermatology and Probity Medical Research, Peterborough, ON, Canada.
  • Cichanowitz N; Queen's University, Kingston, ON, Canada.
  • La Rosa C; Merck & Co., Inc., Kenilworth, NJ, U.S.A.
  • Blauvelt A; Merck & Co., Inc., Kenilworth, NJ, U.S.A.
Br J Dermatol ; 182(6): 1359-1368, 2020 06.
Article in En | MEDLINE | ID: mdl-31487406
ABSTRACT

BACKGROUND:

Chronic psoriasis may require medication adjustments over time.

OBJECTIVES:

To evaluate the efficacy/safety of tildrakizumab in subgroups from the reSURFACE studies (N = 1862) that received continuous dosing, higher/lower dosing, treatment interruption/reinitiation and initiation.

METHODS:

Responders [Psoriasis Area and Severity Index (PASI) ≥ 75%] and partial responders (PASI ≥ 50% to < 75%) in Part 3 of the reSURFACE studies (weeks 28-52 or week 64) who received tildrakizumab 200 mg or 100 mg were rerandomized to the same dosage (T100/T100 or T200/T200), a higher/lower dosage (T100/T200 or T200/T100) or placebo (PBO) (T100/PBO or T200/PBO). Patients receiving PBO who relapsed were reinitiated to tildrakizumab. Etanercept (ETN) week-28 partial responders and nonresponders (PASI < 50%) received tildrakizumab 200 mg (ETN/T200).

RESULTS:

Among T100/T100 and T200/T200 week-28 partial responders, the proportion of patients who achieved as-observed PASI 75 responses increased over time. Among T100/T200 week-28 partial responders, PASI 75 responses increased from week 32 (38·5%) to week 52 (63·2%) and remained consistent in T200/T100 week-28 responders. Among patients who relapsed in the T100/PBO and T200/PBO groups, 86% and 83% of those who reinitiated tildrakizumab achieved PASI 75 by week 64, respectively. Among ETN/T200 week-28 partial responders, PASI 75 responses (nonresponder imputation) increased from week 32 (24·1%) to week 52 (74·7%). PASI 90, PASI 100 and Physician's Global Assessment responses were consistent with PASI 75 results. Treatment was well tolerated.

CONCLUSIONS:

Patients generally fared well with tildrakizumab maintenance, reinitiation, dose adjustment or initiation. What's already known about this topic? Tildrakizumab demonstrated significant efficacy vs. placebo with a positive safety profile during the first 28 weeks of treatment in two randomized double-blind trials. What does this study add? Treatment scenarios with tildrakizumab, such as long-term continuous dosing (up to 64 weeks), treatment interruption/reinitiation and switching from another biologic, can be part of the management of plaque psoriasis with a reasonable expectation of efficacy and tolerability.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psoriasis Type of study: Clinical_trials Limits: Humans Language: En Journal: Br J Dermatol Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psoriasis Type of study: Clinical_trials Limits: Humans Language: En Journal: Br J Dermatol Year: 2020 Document type: Article Affiliation country: