A randomized phase 2a efficacy and safety trial of the topical Janus kinase inhibitor tofacitinib in the treatment of chronic plaque psoriasis

Summary Background Tofacitinib (CP‐690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory diseases including psoriasis. Objectives This phase 2a study aimed to assess the efficacy, systemic safety, local tolerability and systemic ph...

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Published inBritish journal of dermatology (1951) Vol. 169; no. 1; pp. 137 - 145
Main Authors Ports, W.C., Khan, S., Lan, S., Lamba, M., Bolduc, C., Bissonnette, R., Papp, K.
Format Journal Article
LanguageEnglish
Published Oxford Blackwell Publishing Ltd 01.07.2013
Wiley-Blackwell
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Abstract Summary Background Tofacitinib (CP‐690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory diseases including psoriasis. Objectives This phase 2a study aimed to assess the efficacy, systemic safety, local tolerability and systemic pharmacokinetics of topical tofacitinib in mild‐to‐moderate plaque psoriasis. Methods Two tofacitinib ointment formulations were evaluated in this multicentre, double‐blind, vehicle‐controlled trial (NCT01246583). Seventy‐one patients were randomized 2 : 1 : 2 : 1 to 2% tofacitinib ointment 1, vehicle 1, 2% tofacitinib ointment 2 and vehicle 2, each administered twice daily for 4 weeks to a single fixed 300 cm2 treatment area containing a target plaque with or without one or more nontarget plaques and normal skin. Results The primary endpoint of percentage change from baseline in the Target Plaque Severity Score at week 4 demonstrated statistically significant improvement for ointment 1 [least squares mean (LSM) –54·4%] vs. vehicle 1 (LSM –41·5%), but not ointment 2 (LSM –24·2%) vs. vehicle 2 (LSM –17·2%). Secondary endpoints (target plaque area and Itch Severity Item) improved similarly for tofacitinib ointment vs. corresponding vehicle. Adverse event (AE) occurrence was similar across treatment groups. All AEs were mild or moderate and none were serious or led to subject discontinuation. One application‐site AE (erythema) was reported. Tofacitinib mean systemic exposure was minimal and was greater for ointment 1 than for ointment 2. Conclusions Tofacitinib ointment 1 was well tolerated and efficacious compared with vehicle for the treatment of plaque psoriasis. Further study of topical tofacitinib for psoriasis treatment is warranted. What's already known about this topic? Janus kinase (JAK) signalling has been implicated in the pathogenesis of psoriasis. Tofacitinib (CP‐690,550) is a novel, small‐molecule JAK inhibitor in development for the treatment of several inflammatory diseases: it has demonstrated efficacy in a phase 2b study in moderate‐to‐severe plaque psoriasis when given orally. Topical therapy is the more commonly used therapeutic option for psoriasis, but there is a need for improved topical treatments. What does this study add? In this phase 2a study, tofacitinib in an ointment formulation demonstrated efficacy, systemic safety and local tolerability during 4 weeks of treatment in patients with mild‐to‐moderate chronic plaque psoriasis. Dermal penetration of tofacitinib, a small‐molecule, was demonstrated. Topical application of tofacitinib has the potential to provide an additional therapeutic option for patients with plaque psoriasis.
AbstractList Summary Background Tofacitinib (CP‐690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory diseases including psoriasis. Objectives This phase 2a study aimed to assess the efficacy, systemic safety, local tolerability and systemic pharmacokinetics of topical tofacitinib in mild‐to‐moderate plaque psoriasis. Methods Two tofacitinib ointment formulations were evaluated in this multicentre, double‐blind, vehicle‐controlled trial (NCT01246583). Seventy‐one patients were randomized 2 : 1 : 2 : 1 to 2% tofacitinib ointment 1, vehicle 1, 2% tofacitinib ointment 2 and vehicle 2, each administered twice daily for 4 weeks to a single fixed 300 cm2 treatment area containing a target plaque with or without one or more nontarget plaques and normal skin. Results The primary endpoint of percentage change from baseline in the Target Plaque Severity Score at week 4 demonstrated statistically significant improvement for ointment 1 [least squares mean (LSM) –54·4%] vs. vehicle 1 (LSM –41·5%), but not ointment 2 (LSM –24·2%) vs. vehicle 2 (LSM –17·2%). Secondary endpoints (target plaque area and Itch Severity Item) improved similarly for tofacitinib ointment vs. corresponding vehicle. Adverse event (AE) occurrence was similar across treatment groups. All AEs were mild or moderate and none were serious or led to subject discontinuation. One application‐site AE (erythema) was reported. Tofacitinib mean systemic exposure was minimal and was greater for ointment 1 than for ointment 2. Conclusions Tofacitinib ointment 1 was well tolerated and efficacious compared with vehicle for the treatment of plaque psoriasis. Further study of topical tofacitinib for psoriasis treatment is warranted. What's already known about this topic? Janus kinase (JAK) signalling has been implicated in the pathogenesis of psoriasis. Tofacitinib (CP‐690,550) is a novel, small‐molecule JAK inhibitor in development for the treatment of several inflammatory diseases: it has demonstrated efficacy in a phase 2b study in moderate‐to‐severe plaque psoriasis when given orally. Topical therapy is the more commonly used therapeutic option for psoriasis, but there is a need for improved topical treatments. What does this study add? In this phase 2a study, tofacitinib in an ointment formulation demonstrated efficacy, systemic safety and local tolerability during 4 weeks of treatment in patients with mild‐to‐moderate chronic plaque psoriasis. Dermal penetration of tofacitinib, a small‐molecule, was demonstrated. Topical application of tofacitinib has the potential to provide an additional therapeutic option for patients with plaque psoriasis.
Tofacitinib (CP-690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory diseases including psoriasis. This phase 2a study aimed to assess the efficacy, systemic safety, local tolerability and systemic pharmacokinetics of topical tofacitinib in mild-to-moderate plaque psoriasis. Two tofacitinib ointment formulations were evaluated in this multicentre, double-blind, vehicle-controlled trial (NCT01246583). Seventy-one patients were randomized 2 : 1 : 2 : 1 to 2% tofacitinib ointment 1, vehicle 1, 2% tofacitinib ointment 2 and vehicle 2, each administered twice daily for 4 weeks to a single fixed 300 cm(2) treatment area containing a target plaque with or without one or more nontarget plaques and normal skin. The primary endpoint of percentage change from baseline in the Target Plaque Severity Score at week 4 demonstrated statistically significant improvement for ointment 1 [least squares mean (LSM) -54.4%] vs. vehicle 1 (LSM -41.5%), but not ointment 2 (LSM -24.2%) vs. vehicle 2 (LSM -17.2%). Secondary endpoints (target plaque area and Itch Severity Item) improved similarly for tofacitinib ointment vs. corresponding vehicle. Adverse event (AE) occurrence was similar across treatment groups. All AEs were mild or moderate and none were serious or led to subject discontinuation. One application-site AE (erythema) was reported. Tofacitinib mean systemic exposure was minimal and was greater for ointment 1 than for ointment 2. Tofacitinib ointment 1 was well tolerated and efficacious compared with vehicle for the treatment of plaque psoriasis. Further study of topical tofacitinib for psoriasis treatment is warranted.
Tofacitinib (CP-690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory diseases including psoriasis.BACKGROUNDTofacitinib (CP-690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory diseases including psoriasis.This phase 2a study aimed to assess the efficacy, systemic safety, local tolerability and systemic pharmacokinetics of topical tofacitinib in mild-to-moderate plaque psoriasis.OBJECTIVESThis phase 2a study aimed to assess the efficacy, systemic safety, local tolerability and systemic pharmacokinetics of topical tofacitinib in mild-to-moderate plaque psoriasis.Two tofacitinib ointment formulations were evaluated in this multicentre, double-blind, vehicle-controlled trial (NCT01246583). Seventy-one patients were randomized 2 : 1 : 2 : 1 to 2% tofacitinib ointment 1, vehicle 1, 2% tofacitinib ointment 2 and vehicle 2, each administered twice daily for 4 weeks to a single fixed 300 cm(2) treatment area containing a target plaque with or without one or more nontarget plaques and normal skin.METHODSTwo tofacitinib ointment formulations were evaluated in this multicentre, double-blind, vehicle-controlled trial (NCT01246583). Seventy-one patients were randomized 2 : 1 : 2 : 1 to 2% tofacitinib ointment 1, vehicle 1, 2% tofacitinib ointment 2 and vehicle 2, each administered twice daily for 4 weeks to a single fixed 300 cm(2) treatment area containing a target plaque with or without one or more nontarget plaques and normal skin.The primary endpoint of percentage change from baseline in the Target Plaque Severity Score at week 4 demonstrated statistically significant improvement for ointment 1 [least squares mean (LSM) -54.4%] vs. vehicle 1 (LSM -41.5%), but not ointment 2 (LSM -24.2%) vs. vehicle 2 (LSM -17.2%). Secondary endpoints (target plaque area and Itch Severity Item) improved similarly for tofacitinib ointment vs. corresponding vehicle. Adverse event (AE) occurrence was similar across treatment groups. All AEs were mild or moderate and none were serious or led to subject discontinuation. One application-site AE (erythema) was reported. Tofacitinib mean systemic exposure was minimal and was greater for ointment 1 than for ointment 2.RESULTSThe primary endpoint of percentage change from baseline in the Target Plaque Severity Score at week 4 demonstrated statistically significant improvement for ointment 1 [least squares mean (LSM) -54.4%] vs. vehicle 1 (LSM -41.5%), but not ointment 2 (LSM -24.2%) vs. vehicle 2 (LSM -17.2%). Secondary endpoints (target plaque area and Itch Severity Item) improved similarly for tofacitinib ointment vs. corresponding vehicle. Adverse event (AE) occurrence was similar across treatment groups. All AEs were mild or moderate and none were serious or led to subject discontinuation. One application-site AE (erythema) was reported. Tofacitinib mean systemic exposure was minimal and was greater for ointment 1 than for ointment 2.Tofacitinib ointment 1 was well tolerated and efficacious compared with vehicle for the treatment of plaque psoriasis. Further study of topical tofacitinib for psoriasis treatment is warranted.CONCLUSIONSTofacitinib ointment 1 was well tolerated and efficacious compared with vehicle for the treatment of plaque psoriasis. Further study of topical tofacitinib for psoriasis treatment is warranted.
Author Papp, K.
Khan, S.
Bolduc, C.
Ports, W.C.
Bissonnette, R.
Lan, S.
Lamba, M.
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Issue 1
Keywords Local administration
Skin disease
Chronic
Randomization
Phase
Treatment
Psoriasis
Dermatology
Tyrosine kinase inhibitor
Clinical trial
Safety
Language English
License CC BY 4.0
The Authors © 2013 Pfizer Inc BJD © 2013 British Association of Dermatologists.
Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
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Data S1. CYP3A4 inhibitors and inducers. Table S1. List of prohibited potent inhibitors and inducers of CYP3A4. Table S2. List of permitted moderate inhibitors and inducers of CYP3A4.
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Funding source This study was funded by Pfizer Inc.
Conflicts of interest See Appendix.
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2011; 63
2009; 100
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2011; 15
2009; 361
2009; 129
2012; 367
2007; 21
2007; 44
2012; 67
2010; 7
2012; 64
2011; 186
19225543 - J Invest Dermatol. 2009 Sep;129(9):2299-302
17312100 - J Immunol. 2007 Mar 1;178(5):2623-9
19641206 - N Engl J Med. 2009 Jul 30;361(5):496-509
23834112 - Br J Dermatol. 2013 Jul;169(1):2-3
20096156 - Actas Dermosifiliogr. 2009 Dec;100 Suppl 2:2-13
20003607 - Expert Rev Mol Med. 2009;11:e38
22121136 - Ann Rheum Dis. 2012 Mar;71(3):440-7
22894574 - N Engl J Med. 2012 Aug 16;367(7):616-24
21383241 - J Immunol. 2011 Apr 1;186(7):4234-43
21084214 - Cytokine Growth Factor Rev. 2010 Dec;21(6):425-34
22873531 - N Engl J Med. 2012 Aug 9;367(6):508-19
22006202 - Arthritis Rheum. 2012 Apr;64(4):970-81
22281165 - J Am Acad Dermatol. 2012 Oct;67(4):658-64
20055694 - J Dermatolog Treat. 2010 Jan;21(1):13-22
21952978 - Arthritis Rheum. 2012 Mar;64(3):617-29
22561807 - Nat Med. 2012 May;18(5):638
22873530 - N Engl J Med. 2012 Aug 9;367(6):495-507
21781627 - J Cutan Med Surg. 2011 Jul-Aug;15(4):210-9
22924949 - Br J Dermatol. 2012 Sep;167(3):668-77
17373972 - J Eur Acad Dermatol Venereol. 2007 Apr;21(4):466-72
20701804 - J Inflamm (Lond). 2010 Aug 11;7:41
17208301 - Mol Immunol. 2007 Apr;44(10):2497-506
9390335 - Br J Dermatol. 1997 Oct;137(4):581-6
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Snippet Summary Background Tofacitinib (CP‐690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory...
Tofacitinib (CP-690,550) is a novel Janus kinase inhibitor in development as an oral formulation for the treatment of several inflammatory diseases including...
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StartPage 137
SubjectTerms Administration, Cutaneous
Adult
Aged
Biological and medical sciences
Chronic Disease
Dermatologic Agents - administration & dosage
Dermatologic Agents - adverse effects
Dermatologic Agents - pharmacokinetics
Dermatology
Double-Blind Method
Drug Administration Schedule
Female
Humans
Male
Medical sciences
Middle Aged
Ointments
Original
Piperidines - administration & dosage
Piperidines - adverse effects
Piperidines - pharmacokinetics
Protein Kinase Inhibitors - administration & dosage
Protein Kinase Inhibitors - adverse effects
Protein Kinase Inhibitors - pharmacokinetics
Psoriasis - drug therapy
Psoriasis. Parapsoriasis. Lichen
Pyrimidines - administration & dosage
Pyrimidines - adverse effects
Pyrimidines - pharmacokinetics
Pyrroles - administration & dosage
Pyrroles - adverse effects
Pyrroles - pharmacokinetics
Treatment Outcome
Young Adult
Title A randomized phase 2a efficacy and safety trial of the topical Janus kinase inhibitor tofacitinib in the treatment of chronic plaque psoriasis
URI https://api.istex.fr/ark:/67375/WNG-RS57W7DM-5/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fbjd.12266
https://www.ncbi.nlm.nih.gov/pubmed/23387374
https://www.proquest.com/docview/1399263664
https://pubmed.ncbi.nlm.nih.gov/PMC3761190
Volume 169
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