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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Veröffentlicht in:British journal of dermatology (1951) 2013-07, Vol.169 (1), p.137-145
Hauptverfasser: Ports, W.C., Khan, S., Lan, S., Lamba, M., Bolduc, C., Bissonnette, R., Papp, K.
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container_end_page 145
container_issue 1
container_start_page 137
container_title British journal of dermatology (1951)
container_volume 169
creator Ports, W.C.
Khan, S.
Lan, S.
Lamba, M.
Bolduc, C.
Bissonnette, R.
Papp, K.
description 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 pen
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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.</description><identifier>ISSN: 0007-0963</identifier><identifier>EISSN: 1365-2133</identifier><identifier>DOI: 10.1111/bjd.12266</identifier><identifier>PMID: 23387374</identifier><identifier>CODEN: BJDEAZ</identifier><language>eng</language><publisher>Oxford: Blackwell Publishing Ltd</publisher><subject>Administration, Cutaneous ; Adult ; Aged ; Biological and medical sciences ; Chronic Disease ; Dermatologic Agents - administration &amp; 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 &amp; dosage ; Piperidines - adverse effects ; Piperidines - pharmacokinetics ; Protein Kinase Inhibitors - administration &amp; dosage ; Protein Kinase Inhibitors - adverse effects ; Protein Kinase Inhibitors - pharmacokinetics ; Psoriasis - drug therapy ; Psoriasis. Parapsoriasis. Lichen ; Pyrimidines - administration &amp; dosage ; Pyrimidines - adverse effects ; Pyrimidines - pharmacokinetics ; Pyrroles - administration &amp; dosage ; Pyrroles - adverse effects ; Pyrroles - pharmacokinetics ; Treatment Outcome ; Young Adult</subject><ispartof>British journal of dermatology (1951), 2013-07, Vol.169 (1), p.137-145</ispartof><rights>The Authors © 2013 Pfizer Inc BJD © 2013 British Association of Dermatologists</rights><rights>2014 INIST-CNRS</rights><rights>The Authors © 2013 Pfizer Inc BJD © 2013 British Association of Dermatologists.</rights><rights>Copyright © 2013 British Association of Dermatologists 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbjd.12266$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbjd.12266$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=27605089$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23387374$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ports, W.C.</creatorcontrib><creatorcontrib>Khan, S.</creatorcontrib><creatorcontrib>Lan, S.</creatorcontrib><creatorcontrib>Lamba, M.</creatorcontrib><creatorcontrib>Bolduc, C.</creatorcontrib><creatorcontrib>Bissonnette, R.</creatorcontrib><creatorcontrib>Papp, K.</creatorcontrib><title>A randomized phase 2a efficacy and safety trial of the topical Janus kinase inhibitor tofacitinib in the treatment of chronic plaque psoriasis</title><title>British journal of dermatology (1951)</title><addtitle>Br J Dermatol</addtitle><description>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.</description><subject>Administration, Cutaneous</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Chronic Disease</subject><subject>Dermatologic Agents - administration &amp; dosage</subject><subject>Dermatologic Agents - adverse effects</subject><subject>Dermatologic Agents - pharmacokinetics</subject><subject>Dermatology</subject><subject>Double-Blind Method</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Ointments</subject><subject>Original</subject><subject>Piperidines - administration &amp; dosage</subject><subject>Piperidines - adverse effects</subject><subject>Piperidines - pharmacokinetics</subject><subject>Protein Kinase Inhibitors - administration &amp; dosage</subject><subject>Protein Kinase Inhibitors - adverse effects</subject><subject>Protein Kinase Inhibitors - pharmacokinetics</subject><subject>Psoriasis - drug therapy</subject><subject>Psoriasis. Parapsoriasis. Lichen</subject><subject>Pyrimidines - administration &amp; dosage</subject><subject>Pyrimidines - adverse effects</subject><subject>Pyrimidines - pharmacokinetics</subject><subject>Pyrroles - administration &amp; dosage</subject><subject>Pyrroles - adverse effects</subject><subject>Pyrroles - pharmacokinetics</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0007-0963</issn><issn>1365-2133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNpVUctu1DAUtRAVHQoLfgB5wzKtHY_teINUWiitWpB4qEvrxrHJbTNJGnuA4SP6zfV02gG88ZXPw1fnEPKKs32ez0F91ezzslTqCZlxoWRRciGekhljTBfMKLFLnsd4xRgXTLJnZLcUotJCz2fk9pBO0DfDAv_4ho4tRE9LoD4EdOBWNGM0QvBpRdOE0NEh0NR6moYxEzp6Bv0y0mvs10LsW6wxDVOGAzhM2GOdXzeKyUNa-D6tLVw7DT06OnZws_R0jEM2jxhfkJ0AXfQvH-498v3D-29HH4vzzyenR4fnBeatVeEap6RT3NRzr0B4YDpop1TpwUkhTWW0n_sKmGpkCIYZ0_A81No5kJWsxR55u_Edl_XCNy6vNUFnxwkXMK3sAGj_R3ps7Y_hpxVacW5YNnj9r8FW-ZhsJrx5IEDMQYWcssP4l6dVrqIymXew4f3Czq-2OGd2Xa3N1dr7au27s-P7ISuKjQJj8r-3CpiurcpfS3v56cR--Sr1pT6-sFLcAbXNqRU</recordid><startdate>201307</startdate><enddate>201307</enddate><creator>Ports, W.C.</creator><creator>Khan, S.</creator><creator>Lan, S.</creator><creator>Lamba, M.</creator><creator>Bolduc, C.</creator><creator>Bissonnette, R.</creator><creator>Papp, K.</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>24P</scope><scope>WIN</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>5PM</scope></search><sort><creationdate>201307</creationdate><title>A randomized phase 2a efficacy and safety trial of the topical Janus kinase inhibitor tofacitinib in the treatment of chronic plaque psoriasis</title><author>Ports, W.C. ; Khan, S. ; Lan, S. ; Lamba, M. ; Bolduc, C. ; Bissonnette, R. ; Papp, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3746-cdc65c619b4e6a3ea07f7c662eac5359897e4e8a06d5ff9099d15ffb7cca585b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Administration, Cutaneous</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Chronic Disease</topic><topic>Dermatologic Agents - administration &amp; dosage</topic><topic>Dermatologic Agents - adverse effects</topic><topic>Dermatologic Agents - pharmacokinetics</topic><topic>Dermatology</topic><topic>Double-Blind Method</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Ointments</topic><topic>Original</topic><topic>Piperidines - administration &amp; dosage</topic><topic>Piperidines - adverse effects</topic><topic>Piperidines - pharmacokinetics</topic><topic>Protein Kinase Inhibitors - administration &amp; dosage</topic><topic>Protein Kinase Inhibitors - adverse effects</topic><topic>Protein Kinase Inhibitors - pharmacokinetics</topic><topic>Psoriasis - drug therapy</topic><topic>Psoriasis. Parapsoriasis. Lichen</topic><topic>Pyrimidines - administration &amp; dosage</topic><topic>Pyrimidines - adverse effects</topic><topic>Pyrimidines - pharmacokinetics</topic><topic>Pyrroles - administration &amp; dosage</topic><topic>Pyrroles - adverse effects</topic><topic>Pyrroles - pharmacokinetics</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ports, W.C.</creatorcontrib><creatorcontrib>Khan, S.</creatorcontrib><creatorcontrib>Lan, S.</creatorcontrib><creatorcontrib>Lamba, M.</creatorcontrib><creatorcontrib>Bolduc, C.</creatorcontrib><creatorcontrib>Bissonnette, R.</creatorcontrib><creatorcontrib>Papp, K.</creatorcontrib><collection>Istex</collection><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of dermatology (1951)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ports, W.C.</au><au>Khan, S.</au><au>Lan, S.</au><au>Lamba, M.</au><au>Bolduc, C.</au><au>Bissonnette, R.</au><au>Papp, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A randomized phase 2a efficacy and safety trial of the topical Janus kinase inhibitor tofacitinib in the treatment of chronic plaque psoriasis</atitle><jtitle>British journal of dermatology (1951)</jtitle><addtitle>Br J Dermatol</addtitle><date>2013-07</date><risdate>2013</risdate><volume>169</volume><issue>1</issue><spage>137</spage><epage>145</epage><pages>137-145</pages><issn>0007-0963</issn><eissn>1365-2133</eissn><coden>BJDEAZ</coden><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.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>23387374</pmid><doi>10.1111/bjd.12266</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Access via Wiley Online Library; Oxford University Press Journals All Titles (1996-Current)
subjects 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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