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 in | British journal of dermatology (1951) Vol. 169; no. 1; pp. 137 - 145 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Blackwell Publishing Ltd
01.07.2013
Wiley-Blackwell |
Subjects | |
Online Access | Get full text |
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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. |
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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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Copyright | The Authors © 2013 Pfizer Inc BJD © 2013 British Association of Dermatologists 2014 INIST-CNRS The Authors © 2013 Pfizer Inc BJD © 2013 British Association of Dermatologists. Copyright © 2013 British Association of Dermatologists 2013 |
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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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Notes | ark:/67375/WNG-RS57W7DM-5 istex:02E698EA47C6757E435665A854A360FD35B77109 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. ArticleID:BJD12266 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 Funding source This study was funded by Pfizer Inc. Conflicts of interest See Appendix. |
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References_xml | – reference: van der Heijde D, Tanaka Y, Fleischmann R et al. Tofacitinib (CP-690,550), an oral Janus kinase inhibitor, in combination with methotrexate reduced the progression of structural damage in patients with rheumatoid arthritis: a 24-month Phase 3 study. Arthritis Rheum 2011; 63(Suppl. 10):S107. – reference: Boy MG, Wang C, Wilkinson BE et al. Double-blind, placebo-controlled, dose-escalation study to evaluate the pharmacologic effect of CP-690,550 in patients with psoriasis. J Invest Dermatol 2009; 129:2299-302. – reference: Fleischmann R, Kremer J, Cush J et al. Placebo-controlled trial of tofacitinib monotherapy in rheumatoid arthritis. N Engl J Med 2012; 367:495-507. – reference: Williams SC. New biologic drugs get under the skin of psoriasis. Nat Med 2012; 18:638. – reference: Racz E, Prens EP. Molecular pathophysiology of psoriasis and molecular targets of antipsoriatic therapy. Expert Rev Mol Med 2009; 11:e38. – reference: Murray PJ. 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pharmacologic effect of CP‐690,550 in patients with psoriasis publication-title: J Invest Dermatol – volume: 186 start-page: 4234 year: 2011 end-page: 43 article-title: Modulation of innate and adaptive immune responses by tofacitinib (CP‐690,550) publication-title: J Immunol – volume: 361 start-page: 496 year: 2009 end-page: 509 article-title: Psoriasis publication-title: N Engl J Med – volume: 71 start-page: 440 year: 2012 end-page: 7 article-title: The JAK inhibitor CP‐690,550 (tofacitinib) inhibits TNF‐induced chemokine expression in fibroblast‐like synoviocytes: autocrine role of type I interferon publication-title: Ann Rheum Dis – volume: 21 start-page: 13 year: 2010 end-page: 22 article-title: Treatment of plaque psoriasis with the two‐compound product calcipotriol/betamethasone dipropionate versus both monotherapies: an immunohistochemical study publication-title: J Dermatolog Treat – volume: 11 start-page: e38 year: 2009 article-title: Molecular pathophysiology of psoriasis 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combination with traditional DMARDS: a Phase 3 efficacy and safety study in patients with active rheumatoid arthritis with an inadequate response to DMARDs publication-title: Ann Rheum Dis – volume: 21 start-page: 466 year: 2007 end-page: 72 article-title: An investigator‐masked comparison of the efficacy and safety of twice daily applications of calcitriol 3 microg/g ointment vs. calcipotriol 50 microg/g ointment in subjects with mild to moderate chronic plaque‐type psoriasis publication-title: J Eur Acad Dermatol Venereol – reference: 22894574 - N Engl J Med. 2012 Aug 16;367(7):616-24 – reference: 9390335 - Br J Dermatol. 1997 Oct;137(4):581-6 – reference: 21383241 - J Immunol. 2011 Apr 1;186(7):4234-43 – reference: 17373972 - J Eur Acad Dermatol Venereol. 2007 Apr;21(4):466-72 – reference: 19225543 - J Invest Dermatol. 2009 Sep;129(9):2299-302 – reference: 22281165 - J Am Acad Dermatol. 2012 Oct;67(4):658-64 – reference: 20096156 - Actas Dermosifiliogr. 2009 Dec;100 Suppl 2:2-13 – reference: 22561807 - Nat Med. 2012 May;18(5):638 – reference: 17312100 - J Immunol. 2007 Mar 1;178(5):2623-9 – reference: 21781627 - J Cutan Med Surg. 2011 Jul-Aug;15(4):210-9 – reference: 22924949 - Br J Dermatol. 2012 Sep;167(3):668-77 – reference: 20003607 - Expert Rev Mol Med. 2009;11:e38 – reference: 21084214 - Cytokine Growth Factor Rev. 2010 Dec;21(6):425-34 – reference: 17208301 - Mol Immunol. 2007 Apr;44(10):2497-506 – reference: 20701804 - J Inflamm (Lond). 2010 Aug 11;7:41 – reference: 21952978 - Arthritis Rheum. 2012 Mar;64(3):617-29 – reference: 22873531 - N Engl J Med. 2012 Aug 9;367(6):508-19 – reference: 22873530 - N Engl J Med. 2012 Aug 9;367(6):495-507 – reference: 22121136 - Ann Rheum Dis. 2012 Mar;71(3):440-7 – reference: 22006202 - Arthritis Rheum. 2012 Apr;64(4):970-81 – reference: 23834112 - Br J Dermatol. 2013 Jul;169(1):2-3 – reference: 20055694 - J Dermatolog Treat. 2010 Jan;21(1):13-22 – reference: 19641206 - N Engl J Med. 2009 Jul 30;361(5):496-509 |
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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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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 |
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