We'd like your feedback
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Incyte Corporation Call Center (ex-US)
+800 00027423
eumedinfo@incyte.com
Incyte Corporation Call Center (US)
1.855.463.3463
medinfo@incyte.com
Prurigo Neurodermatitis
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
The purpose of this study is to evaluate effect of povorcitinib on itch and skin lesions in participants with prurigo nodularis.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
You can take part if:
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Incyte Corporation Call Center (US)
1.855.463.3463
medinfo@incyte.com
Incyte Corporation Call Center (ex-US)
+800 00027423
eumedinfo@incyte.com
The study is sponsored by Incyte Corporation
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
