A double-blind, randomized, placebo- and positive-controlled phase III trial of 1% benvitimod cream in mild-to-moderate plaque psoriasis

Supplemental Digital Content is available in the text Abstract Background Benvitimod cream, a novel synthetic small molecule, was effective in treating mild-to-moderate plaque psoriasis. We conducted a phase III clinical trial to assess the efficacy and safety of benvitimod cream in patients with mild-to-moderate plaque psoriasis. Methods We randomly assigned 686 patients (2:1:1) to receive 1% benvitimod cream, 0.005% calcipotriol ointment or placebo twice a day for 12 weeks. The primary efficacy end points were the percentage of patients with a 75% or greater reduction from baseline in the psoriasis area and severity index (PASI 75) score and with a score of 0 or 1 in static physician's global assessment (sPGA) at week 12. Results The results showed that 50.4% of patients in the benvitimod group achieved PASI 75, which was significantly higher than that in the calcipotriol (38.5%, P < 0.05) and placebo (13.9%, P < 0.05) groups. The proportion of patients achieving an sPGA score 0 or 1 was 66.3% in the benvitimod group and 63.9% in the calcipotriol group, which were both significantly higher than that in the placebo group (34%, P < 0.05). In the long-term follow-up study, 50.8% of patients experienced recurrence. After retreatment with 1% benvitimod, 73.3% of patients achieved an sPGA score of 0 or 1 again at week 52. Adverse events included application site irritation, follicular papules, and contact dermatitis. No systemic adverse reactions were reported. Conclusion During this 12-week study, benvitimod cream was demonstrated with high effectiveness and safety in patients with mild-to-moderate plaque psoriasis. Trial Registration Chinese Clinical Trial Registry (ChiCTR), ChiCTR-TRC-13003259; http://www.chictr.org.cn/showprojen.aspx?proj=6300.

[1]  C. Dolianitis,et al.  Treatment modalities and risk of adverse events associated with biologic therapy: A 10‐year observational review of the Australasian Psoriasis Registry , 2020, The Australasian journal of dermatology.

[2]  L. Gold,et al.  A Phase IIb, Randomized Clinical Trial of Tapinarof Cream for the Treatment of Plaque Psoriasis: Secondary Efficacy and Patient-Reported Outcomes. , 2020, Journal of the American Academy of Dermatology.

[3]  J. Rosso Topical Corticosteroid Therapy for Psoriasis-A Review of Clobetasol Propionate 0.025% Cream and the Clinical Relevance of Penetration Modification. , 2020 .

[4]  J. D. Del Rosso Topical Corticosteroid Therapy for Psoriasis-A Review of Clobetasol Propionate 0.025% Cream and the Clinical Relevance of Penetration Modification. , 2020, The Journal of clinical and aesthetic dermatology.

[5]  Ping Liu,et al.  Aryl hydrocarbon receptor expression in serum, peripheral blood mononuclear cells, and skin lesions of patients with atopic dermatitis and its correlation with disease severity , 2019, Chinese medical journal.

[6]  G. Han,et al.  New and Emerging Topical Therapies for Psoriasis and Atopic Dermatitis. , 2019, The Journal of clinical and aesthetic dermatology.

[7]  H. Merk [The aryl hydrocarbon receptor as the target structure for new drugs in psoriasis and atopic dermatitis]. , 2019, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

[8]  M. Furue,et al.  Aryl Hydrocarbon Receptor in Atopic Dermatitis and Psoriasis , 2019, International journal of molecular sciences.

[9]  J. Peppers,et al.  Phase 2, randomized dose‐finding study of tapinarof (GSK2894512 cream) for the treatment of plaque psoriasis , 2019, Journal of the American Academy of Dermatology.

[10]  J. Weinberg,et al.  Update on the pathophysiology of psoriasis. , 2018, Cutis.

[11]  E. Kulakov,et al.  Psoriasis. , 2018, British journal of hospital medicine.

[12]  Wen-Ming Wang,et al.  Skin Microbiome: An Actor in the Pathogenesis of Psoriasis , 2018, Chinese medical journal.

[13]  H. Jin,et al.  Vitamin D and Cardiovascular Risk in Children , 2017, Chinese medical journal.

[14]  J. Yeung,et al.  Diagnosis and management of psoriasis. , 2017, Canadian family physician Medecin de famille canadien.

[15]  S. John,et al.  A systematic review of worldwide epidemiology of psoriasis , 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

[16]  M. Oray,et al.  Long-term side effects of glucocorticoids , 2016, Expert opinion on drug safety.

[17]  J. Zhang,et al.  Randomized, double‐blind, placebo‐controlled, multiple‐dose study of the safety, tolerability and pharmacokinetics of benvitimod, a candidate drug for the treatment of psoriasis , 2014, Journal of clinical pharmacy and therapeutics.

[18]  L. You,et al.  Vitamin D status and the risk of pancreatic cancer: a meta‐analysis , 2013, Chinese medical journal.

[19]  J. Webster,et al.  Identification of two pigments and a hydroxystilbene antibiotic from Photorhabdus luminescens , 1995, Applied and environmental microbiology.

[20]  L. Parish,et al.  Topical Corticosteroids , 1985, International journal of dermatology.