- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05722912
Expanded Access of Ruxolitinib Cream to Treat a Single Patient With cGVHD
January 26, 2023 updated by: Incyte Corporation
To provide ruxolitinib through an expanded access to treat a single patient with cGVHD
Study Overview
Status
Approved for marketing
Conditions
Intervention / Treatment
Study Type
Expanded Access
Expanded Access Type
- Individual Patients
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Pooja Khandelwal, MD, Children's Hospital Medical Center, Cincinnati
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
October 4, 2022
First Submitted That Met QC Criteria
January 26, 2023
First Posted (Actual)
February 10, 2023
Study Record Updates
Last Update Posted (Actual)
February 10, 2023
Last Update Submitted That Met QC Criteria
January 26, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- I 18424-22-02
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Incyte CorporationCompletedGraft-versus-host Disease (GVHD)United States, Spain, Belgium, France, Italy, Finland, United Kingdom, Switzerland, Germany, Israel, Austria, Australia, New Zealand, Poland, Portugal, Taiwan, South Korea, Czechia, Greece
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Incyte CorporationCompletedGraft-versus-host Disease (GVHD)United States
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John LevineCompletedGVHD | Low Risk Acute Graft-versus-host Disease | Graft-versus-host-diseaseUnited States
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The First Affiliated Hospital of Soochow UniversityRecruiting
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Clinical Trials on Ruxolitinib
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Institute of Hematology & Blood Diseases Hospital...Not yet recruitingTransplant-Related Disorder
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Children's Hospital Medical Center, CincinnatiTerminatedChronic Graft Versus Host DiseaseUnited States
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Children's Hospital Medical Center, CincinnatiTerminatedBronchiolitis Obliterans (BO) | Hematopoietic Stem Cell Transplant (HSCT)United States
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Novartis PharmaceuticalsRecruitingSteroid-refractory Acute Graft Versus Host DiseaseChina
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Massachusetts General HospitalIncyte CorporationRecruitingPolycythemia Vera | Essential ThrombocythemiaUnited States
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H. Lee Moffitt Cancer Center and Research InstituteIncyte CorporationActive, not recruitingLeukemia | Chronic Myelomonocytic LeukemiaUnited States
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Massachusetts General HospitalWashington University School of Medicine; Medical College of Wisconsin; Vanderbilt... and other collaboratorsActive, not recruitingAcute Myeloid Leukemia | Allogeneic Stem Cell Transplantation | Acute Myeloid Leukemia in RemissionUnited States
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Julie NangiaIncyte Corporation; Translational Breast Cancer Research ConsortiumCompletedDuctal Carcinoma In Situ | Atypical Ductal Hyperplasia | Atypical Lobular Hyperplasia | Lobular Carcinoma In SituUnited States
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Sidney Kimmel Comprehensive Cancer Center at Johns...Incyte CorporationNot yet recruitingImmune Effector Associated Hemophagocytic Lymphohistiocytosis-like Syndrome (IEC-HS)