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Clinical Trial Details — Status: Approved for marketing

Administrative data

NCT number NCT05722912
Other study ID # I 18424-22-02
Secondary ID
Status Approved for marketing
Phase
First received
Last updated

Study information

Verified date January 2023
Source Incyte Corporation
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

To provide ruxolitinib through an expanded access to treat a single patient with cGVHD


Recruitment information / eligibility

Status Approved for marketing
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility

Study Design


Intervention

Drug:
Ruxolitinib
Ruxolitinib Cream

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Incyte Corporation
See also
  Status Clinical Trial Phase
Completed NCT03112603 - A Study of Ruxolitinib vs Best Available Therapy (BAT) in Patients With Steroid-refractory Chronic Graft vs. Host Disease (GvHD) After Bone Marrow Transplantation (REACH3) Phase 3
Completed NCT03139604 - GRAVITAS-301: A Study of Itacitinib or Placebo in Combination With Corticosteroids for Treatment of Acute Graft-Versus-Host Disease Phase 3
Completed NCT02953678 - A Study of Ruxolitinib in Combination With Corticosteroids for the Treatment of Steroid-Refractory Acute Graft-Versus-Host Disease (REACH-1) Phase 2
Completed NCT02614612 - Study of Itacitinib in Combination With Corticosteroids for the Treatment of Acute GVHD Phase 1
Approved for marketing NCT03147742 - An Expanded Access Program of Ruxolitinib for the Treatment of Graft-Versus-Host Disease Following Allogeneic Hematopoietic Stem Cell Transplant