Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2024-511879-16-00 | Registry Identifier | EU CT Number |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of this study is to evaluate effect of povorcitinib on itch and skin lesions in participants with prurigo nodularis.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Povorcitinib Dose 1 | Experimental | Povorcitinib at the protocol-defined dose. |
|
| Povorcitinib Dose 2 | Experimental | Povorcitinib at the protocol-defined dose. |
|
| Placebo | Placebo Comparator | Placebo at the protocol-defined dose. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Povorcitinib | Drug | Oral Tablet |
|
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of participants achieving Itch NRS4 and IGA-CPG-S-TS at Week 24 | Defined as proportion of participants achieving a ≥ 4-point improvement [reduction] in Itch NRS score from baseline (Itch NRS4) and an IGA CPG-S score of 0 or 1 with a ≥ 2-grade improvement from baseline (IGA-CPG-S-TS). | Week 24 |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of participants achieving Itch NRS4 at Week 24 | Defined as percentage of participants that achieve a ≥ 4-point improvement (reduction) in Itch NRS score from baseline. | Week 24 |
| Proportion of participants achieving IGA-CPG-S-TS at Week 24 |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Other protocol-defined Inclusion/Exclusion Criteria apply.
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Incyte Medical Monitor | Incyte Corporation | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cahaba Dermatology | Birmingham | Alabama | 35244 | United States | ||
| Banner - University Medicine Multispecialty Services Clinic |
Not provided
| Label | URL |
|---|---|
| A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN1) | View source |
Not provided
Incyte shares data with qualified external researchers after a research proposal is submitted. These requests are reviewed and approved by a review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.The trial data availability is according to the criteria and process described on https://www.incyte.com/our-company/compliance-and-transparency
Data will be shared after the primary publication or 2 years after the study has ended for market authorized products and indications.
Data from eligible studies will be shared with qualified researchers according to the criteria and process described in the Data Sharing section of the www.incyteclinicaltrials.com website. For approved requests, the researchers will be granted access to anonymized data under the terms of a data sharing agreement.
Not provided
Not provided
Not provided
Not provided
| Placebo | Drug | Oral Tablet |
|
Defined as percentage of participants that achieve IGA-CPG-S score of 0 or 1 with a ≥ 2 grade improvement from baseline.
| Week 24 |
| Proportion of participants achieving Itch NRS4 at Week 4 | Defined as percentage of participants that achieve a ≥ 4-point improvement (reduction) in Itch NRS score from baseline. | Week 4 |
| Time to Itch NRS4 | Defined as time taken for the participant to achieve a ≥4 improvement in Itch NRS score from baseline. | Up to 52 weeks |
| Change from baseline in Itch NRS score at each postbaseline visit | Itch will be measured using an NRS used to indicate the intensity of the worst itching over the past 24 hours using a 0 to 10 numeric rating scale, where "0" represents "no itching" and "10" represents "worst itching imaginable". | Up to 52 weeks |
| Percent change from baseline in NRS score at each postbaseline visit | Itch will be measured using an NRS used to indicate the intensity of the worst itching over the past 24 hours using a 0 to 10 numeric rating scale, where "0" represents "no itching" and "10" represents "worst itching imaginable". | Up to 52 weeks |
| Proportion of participants achieving Itch NRS4 at each postbaseline visit | Defined as percentage of participants that achieve a ≥ 4-point improvement in Itch NRS score from baseline. | Up to 52 weeks |
| Proportion of participants achieving IGA-CPG-S-TS at each postbaseline visit | Defined as percentage of participants that achieve an IGA-CPG-S score of 0 or 1 with a ≥ 2 grade improvement from baseline. | Up to 52 weeks |
| Proportion of participants achieving Investigator's Global Assessment - Chronic Prurigo Activity (IGA-CPG-A) at each postbaseline visit | Defined as percentage of participants that achieve an IGA-CPG-A score of 0 or 1 with a ≥ 2 grade improvement (reduction) from baseline. | Up to 52 weeks |
| Proportion of participants achieving ≥ 75% healed lesions in Prurigo Activity Score (PAS) at each postbaseline visit | The modified PAS will be used in this study as defined by the protocol. | Up to 52 weeks |
| Proportion of participants achieving Itch NRS4 and IGA-CPG-S-TS at each postbaseline visit | Defined as percentage of participants that achieve a ≥ 4-point improvement (reduction) in Itch NRS score and IGA-CPG-S score of 0 or 1 with a ≥ 2-grade improvement from baseline. | Up to 52 weeks |
| Change from baseline in Dermatology Life Quality Index (DLQI) score at each postbaseline visit. | The DLQI is a simple, 10-question validated questionnaire to measure how much the skin problem has affected the participant over the previous 7 days. | Up to 52 weeks |
| Percent change from baseline in Dermatology Life Quality Index (DLQI) score at each postbaseline visit. | The DLQI is a simple, 10-question validated questionnaire to measure how much the skin problem has affected the participant over the previous 7 days. | Up to 52 weeks |
| Proportion of participants with at least a 4-point decrease in DLQI score from baseline at each postbaseline visit for participants with DLQI score ≥ 4 at baseline | Defined as percentage of participants with at least a 4-point decrease in DLQI score from baseline at each postbaseline visit for participants with DLQI score ≥ 4 at baseline. | Up to 52 weeks |
| Change from baseline in Skin Pain NRS score at each postbaseline visit | Skin Pain NRS is an 11-point scale (0 to10) where 0 is "no pain" and 10 is the "worst pain imaginable". | Up to 52 weeks |
| Percent change from baseline in Skin Pain NRS score at each postbaseline visit | Skin Pain NRS is an 11-point scale (0 to10) where 0 is "no pain" and 10 is the "worst pain imaginable". | Up to 52 weeks |
| Change from baseline in the Hospital Anxiety and Depression Scale (HADS) score at each postbasline visit | HADS is a 14-item questionnaire that assesses the levels of anxiety and depression that a participant is currently experiencing. There are 7 questions each for measuring anxiety and for measuring depression, with 4 possible responses to each question (responses are scored as 0, 1, 2, or 3). | Up to 52 weeks |
| Percent change from baseline in the HADS score at each postbaseline visit | HADS is a 14-item questionnaire that assesses the levels of anxiety and depression that a participant is currently experiencing. There are 7 questions each for measuring anxiety and for measuring depression, with 4 possible responses to each question (responses are scored as 0, 1, 2, or 3). | Up to 52 weeks |
| Change from baseline in EQ-5D-5L score at each postbaseline visit | The EQ-5D-5L questionnaire is a standardized, validated instrument for use as a measure of health outcome. | Up to 52 weeks |
| Percent change from baseline in EQ-5D-5L score at each postbaseline visit | The EQ-5D-5L questionnaire is a standardized, validated instrument for use as a measure of health outcome. | Up to 52 weeks |
| Change in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F) score at each postbaseline visit | The FACIT-F is a 13-item measure that assesses self-reported fatigue and its impact upon daily activities and function over the past 7 days. | Up to 52 weeks |
| Percent change in FACIT-F score at each postbaseline visit | The FACIT-F is a 13-item measure that assesses self-reported fatigue and its impact upon daily activities and function over the past 7 days. | Up to 52 weeks |
| Proportion of participants with at least a ≥ 4-point increase in FACIT-F score at each postbaseline visit for participants with FACIT-F score ≤ 48 at baseline | The FACIT-F is a 13-item measure that assesses self-reported fatigue and its impact upon daily activities and function over the past 7 days. | Up to 52 weeks |
| Number of Participants with Treatment Emergent Adverse Events (TEAE) | Defined as any adverse event either reported for the first time or worsening of a pre-existing event after first dose of study drug. | Up to 52 weeks |
| Tucson |
| Arizona |
| 85718 |
| United States |
| Premier Dermatology Clinical Trials Institute At Northwest Arkansas | Fayetteville | Arkansas | 72703 | United States |
| Burke Pharmaceutical Research | Hot Springs | Arkansas | 71913 | United States |
| Dermatology Research Associates | Los Angeles | California | 90045 | United States |
| Northridge | Northridge | California | 91325 | United States |
| Rendon Center the Dermatology and Aesthetic Center | Boca Raton | Florida | 33486 | United States |
| Driven Research Llc | Coral Gables | Florida | 33134 | United States |
| University of Miami Miller School of Medicine | Miami | Florida | 33136 | United States |
| Research Institute of the Southeast, Llc | West Palm Beach | Florida | 33401 | United States |
| Illinois Dermatology Institute the Chicago Loop | Chicago | Illinois | 60602 | United States |
| Chicago Cosmetic Surgery and Dermatology | Chicago | Illinois | 60654 | United States |
| Center For Medical Dermatology and Immunology Research | Chicago | Illinois | 60657 | United States |
| Northshore University Healthsystem | Skokie | Illinois | 60077 | United States |
| Dermatology Specialists Research Indiana | Clarksville | Indiana | 47129 | United States |
| Oakland Hills Dermatology | Auburn Hills | Michigan | 48326 | United States |
| Hamzavi Dermatology | Fort Gratiot | Michigan | 48059 | United States |
| Somerset Skin Centre | Troy | Michigan | 48084 | United States |
| Medisearch Clinical Trials | Saint Joseph | Missouri | 64506 | United States |
| Washington University School of Medicine | St Louis | Missouri | 63110 | United States |
| The University of New Mexico Unm Health Sciences Center Hsc | Albuquerque | New Mexico | 87131 | United States |
| Montefiore Medical Center | East Syracuse | New York | 13057 | United States |
| Skin Center Dermatology Group | New York | New York | 10956 | United States |
| Stony Brook Dermatology Associates | Stony Brook | New York | 11790 | United States |
| Centricity Research Columbus | Columbus | Ohio | 43213 | United States |
| Wright State Physicians Health Center | Dayton | Ohio | 45324 | United States |
| International Clinical Research Tennessee Llc | Murfreesboro | Tennessee | 37130 | United States |
| Dermatology Treatment and Research Center | Dallas | Texas | 75230 | United States |
| Sweetwater Dermatology | Sugar Land | Texas | 77479 | United States |
| Center For Clinical Studies | Webster | Texas | 77598 | United States |
| Frontier Dermatology | Mill Creek | Washington | 98012 | United States |
| Conexa Investigacion Clinica S.A. | Buenos Aires | 01012 | Argentina |
| Cedic - Centro de Investigacion Clinica | Buenos Aires | C1060ABN | Argentina |
| Instituto de Neumonologia Y Dermatologia | Buenos Aires | C1425BEA | Argentina |
| Instituto de Investigaciones En Alergia Y Enfermedades Respiratorias (Inaer) | Buenos Aires | C1425BEN | Argentina |
| Centro de Investigaciones Medicas Mar Del Plata | Mar del Plata | B7600FYK | Argentina |
| Instituto Especialidades de La Salud Rosario - Clinica Del Torax | Rosario | S2000 | Argentina |
| Investigaciones Reumatologicas Tucuman S.R.L. | San Miguel de Tucumán | T4000AXL | Argentina |
| Medical University Graz University Clinic For Dermatology and Venerology | Graz | 08036 | Austria |
| Wiener Krankenanstaltenverbund (Kav) - Krankenhaus Hietzing Mit Neurologischem Zentrum Rosenhuegel | Vienna | 01130 | Austria |
| Medical Center Medconsult Pleven | Lovech | 05500 | Bulgaria |
| Medical Center Medconsult Pleven Ood | Pleven | 05800 | Bulgaria |
| Diagnostic-Consultative Centre Pulmed Eood | Plovdiv | 04002 | Bulgaria |
| Medical Center Prolet Eood | Rousse | 07000 | Bulgaria |
| Medical Center Unimed Eood | Sevlievo | 05400 | Bulgaria |
| Diagnostic-Consultative Center Ascendent Eood | Sofia | 01202 | Bulgaria |
| Diagnostic-Consultative Center Aleksandrovska Eood | Sofia | 01431 | Bulgaria |
| Dermatology Research Institute | Calgary | Alberta | T2J 7E1 | Canada |
| Rao Dermatology | Edmonton | Alberta | T6G 1C3 | Canada |
| Skin Physicians | Edmonton | Alberta | T6W 4V4 | Canada |
| Alpha Research-Lucere Dermatology and Laser Clinic | Edmonton | Alberta | T6X 0N9 | Canada |
| Park Dermatology | Sherwood Park | Alberta | T8H 0P1 | Canada |
| Simcoderm Medical and Surgical Dermatology Centre | Barrie | Ontario | L4M 7G1 | Canada |
| Skin Health | Cobourg | Ontario | K9A 0Z4 | Canada |
| Centricity Research London Victoria Multispecialty | London | Ontario | N6A 2C2 | Canada |
| Dermeffects | London | Ontario | N6H 5L5 | Canada |
| North York Research Inc. | Toronto | Ontario | M2N 3A6 | Canada |
| Toronto Research Centre | Toronto | Ontario | M3H 5Y8 | Canada |
| Centre de Recherche Dermatologique de Quebec | Québec | Quebec | G1V4X7 | Canada |
| Centre de Recherche Saint-Louis | Québec | Quebec | G1W 4R4 | Canada |
| Sima Recherche | Verdun | Quebec | H4G 3E7 | Canada |
| Skinsense Medical Research | Saskatoon | Saskatchewan | S7K 2C1 | Canada |
| Hopital Prive D Antony | Antony | 92160 | France |
| Hospital Morvan | Brest | 29200 | France |
| Cabinet Medical- Chemin de Paradis | Martigues | 13500 | France |
| Ghrmsa Hopital Emile Muller | Mulhouse | 68100 | France |
| Centre Hospitalier Universitaire de Nantes (Chu de Nantes) - Hopital Hotel Dieu | Nantes | 44093 | France |
| Chu Paris-Gh St-Louis Lariboisiere F.Widal Hopital Saint-Louis | Paris | 75010 | France |
| Hopitaux Drome Nord - Site de Romans Sur Isere | Romans-sur-Isère | 26102 | France |
| Hopital Larrey | Toulouse | 31400 | France |
| Aachen University Hospital | Aachen | 52074 | Germany |
| Fachklinik Bad Bentheim | Bad Bentheim | 48455 | Germany |
| Hautzentrum Friedrichshain Studien | Berlin | 10247 | Germany |
| Charite Universitatsmedizin Berlin | Berlin | 12203 | Germany |
| Klinikum Dortmund Ggmbh | Dortmund | 44137 | Germany |
| Universitaetsklinik Und Poliklinik Fuer Dermatologie Und Venerologie | Halle | 06120 | Germany |
| Universitaetsklinikum Hamburg-Eppendorf | Hamburg | 20246 | Germany |
| Universitatsklinik Heidelberg | Heidelberg | 69115 | Germany |
| Universitaetsklinikum Leipzig | Leipzig | 04103 | Germany |
| Universitaetsklinikum Schleswig-Holstein (Uksh) - Campus Luebeck | Lübeck | 23538 | Germany |
| Universitaetsmedizin Der Johannes - Gutenberg Universitaet Mainz | Mainz | 55131 | Germany |
| Universitaetsklinikum Giessen Und Marburg Gmbh | Marburg | 35043 | Germany |
| Universitaets-Hautklinik Eberhard-Karls-Universitaet Tuebingen | Tübingen | 72076 | Germany |
| Azienda Ospedaliero-Universitaria Policlinico Vittorio Emanuele Ospedale Gaspare Rodolico Di Catania | Catania | 95123 | Italy |
| Clinical Research Centre - Cast | Chieti | 66013 | Italy |
| Azienda Sanitaria Locale 1 (Asl 1) - Ospedale Regionale San Salvatore | L’Aquila | 67100 | Italy |
| Uoc Dermatologia Ospedale Maggiore Policlinico, Fondazione Irccs Ca' Granda | Milan | 20122 | Italy |
| Aou Universita Della Campania Luigi Vanvitelli, Azienda Ospedaliero Universitaria Federico Ii Di Nap | Naples | 80131 | Italy |
| Azienda Ospedaliera Di Perugia | Perugia | 06129 | Italy |
| Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara | Pisa | 56126 | Italy |
| Catholic University of the Sacred Heart | Rome | 00168 | Italy |
| Irccs Istituto Clinico Humanitas | Rozzano | 20089 | Italy |
| Amsterdam Universitair Medisch Centrum, Locatie Amsterdam Medisch Centrum | Amsterdam | 1105 AZ | Netherlands |
| Maxima Medisch Centrum | Veldhoven | 5504 DB | Netherlands |
| Niepubliczny Zaklad Opieki Zdrowotnej Specjalistyczny Osrodek Dermatologiczny Dermal | Bialystok | 15-453 | Poland |
| Uniwersyteckie Centrum Kliniczne | Gdansk | 80-214 | Poland |
| Gyncentrum Sp. Z O.O., Nzoz Holsamed- Oddzial Libero | Katowice | 40-600 | Poland |
| Pro Familia Altera Sp. Z O.O. | Katowice | 40-648 | Poland |
| Centrum Badan Klinicznych, Jagiellonskie Centrum Innowacji Sp.Z.O.O. | Krakow | 30-348 | Poland |
| Diamond Clinic Sp. Z O.O. | Krakow | 31-559 | Poland |
| Niepubliczny Zaklad Opieki Zdrowotnej Med-Laser | Lublin | 20-406 | Poland |
| Mazowieckie Centrum Badan Klinicznych | Pruszków | 05-800 | Poland |
| Laser Clinic | Szczecin | 70-332 | Poland |
| Nzoz Gyncentrum - Oddzial Warszawa | Warsaw | 00-124 | Poland |
| Clinical Research Group Sp. Z.O.O | Warsaw | 01-142 | Poland |
| Centrum Medyczne Evimed | Warsaw | 02-625 | Poland |
| Klinika Ambroziak Sp. Z O.O. | Warsaw | 02-953 | Poland |
| Dermaceum Centrum Badan Klinicznych | Wroclaw | 53-613 | Poland |
| Penta Hospitals Przychodnie, Wroclaw Wejherowska | Wroclaw | 54-239 | Poland |
| Korea University Ansan Hospital | Ansan-si | 15355 | South Korea |
| Soon Chun Hyang University Bucheon Hospital | Bucheon-si | 14584 | South Korea |
| Pusan National University Hospital (Pnuh) | Busan | 49241 | South Korea |
| Pusan National University Yangsan Hospital | Busan | 50612 | South Korea |
| The Catholic University of Korea, Incheon St. Mary'S Hospital | Incheon | 21431 | South Korea |
| Jeonbuk National University Hospital | Jeonju | 54907 | South Korea |
| Seoul National University Hospital | Seoul | 03080 | South Korea |
| Konkuk University Medical Center | Seoul | 05030 | South Korea |
| Inselspital Bern | Bern | 03010 | Switzerland |
| Dsc Clinic Buochs | Buochs | 06374 | Switzerland |
| Universitatsspital Zurich | Zurich | 08091 | Switzerland |