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 |
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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 |
doi_str_mv | 10.1111/bjd.12266 |
format | Article |
fullrecord | <record><control><sourceid>istex_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3761190</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_RS57W7DM_5</sourcerecordid><originalsourceid>FETCH-LOGICAL-i3746-cdc65c619b4e6a3ea07f7c662eac5359897e4e8a06d5ff9099d15ffb7cca585b3</originalsourceid><addsrcrecordid>eNpVUctu1DAUtRAVHQoLfgB5wzKtHY_teINUWiitWpB4qEvrxrHJbTNJGnuA4SP6zfV02gG88ZXPw1fnEPKKs32ez0F91ezzslTqCZlxoWRRciGekhljTBfMKLFLnsd4xRgXTLJnZLcUotJCz2fk9pBO0DfDAv_4ho4tRE9LoD4EdOBWNGM0QvBpRdOE0NEh0NR6moYxEzp6Bv0y0mvs10LsW6wxDVOGAzhM2GOdXzeKyUNa-D6tLVw7DT06OnZws_R0jEM2jxhfkJ0AXfQvH-498v3D-29HH4vzzyenR4fnBeatVeEap6RT3NRzr0B4YDpop1TpwUkhTWW0n_sKmGpkCIYZ0_A81No5kJWsxR55u_Edl_XCNy6vNUFnxwkXMK3sAGj_R3ps7Y_hpxVacW5YNnj9r8FW-ZhsJrx5IEDMQYWcssP4l6dVrqIymXew4f3Czq-2OGd2Xa3N1dr7au27s-P7ISuKjQJj8r-3CpiurcpfS3v56cR--Sr1pT6-sFLcAbXNqRU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A randomized phase 2a efficacy and safety trial of the topical Janus kinase inhibitor tofacitinib in the treatment of chronic plaque psoriasis</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Ports, W.C. ; Khan, S. ; Lan, S. ; Lamba, M. ; Bolduc, C. ; Bissonnette, R. ; Papp, K.</creator><creatorcontrib>Ports, W.C. ; Khan, S. ; Lan, S. ; Lamba, M. ; Bolduc, C. ; Bissonnette, R. ; Papp, K.</creatorcontrib><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><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 & 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</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&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 & 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 & dosage</subject><subject>Piperidines - adverse effects</subject><subject>Piperidines - pharmacokinetics</subject><subject>Protein Kinase Inhibitors - administration & 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 & dosage</subject><subject>Pyrimidines - adverse effects</subject><subject>Pyrimidines - pharmacokinetics</subject><subject>Pyrroles - administration & 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 & 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 & dosage</topic><topic>Piperidines - adverse effects</topic><topic>Piperidines - pharmacokinetics</topic><topic>Protein Kinase Inhibitors - administration & 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 & dosage</topic><topic>Pyrimidines - adverse effects</topic><topic>Pyrimidines - pharmacokinetics</topic><topic>Pyrroles - administration & 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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