Recurrent Classical Hodgkin Lymphoma Clinical Trial
— JeRiCHOOfficial title:
A Phase II, Open-label, Prospective, Non-randomized, Multicenter Clinical Trial With the JAK-inhibitor Ruxolitinib in Patients With Relapsed or Refractory Classical Hodgkin Lymphoma
NCT number | NCT02164500 |
Other study ID # | JeRiCHO |
Secondary ID | |
Status | Completed |
Phase | Phase 2 |
First received | |
Last updated | |
Start date | October 2015 |
Est. completion date | May 17, 2019 |
Verified date | April 2020 |
Source | University of Cologne |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The Purpose of this trial is:
- to determine the overall response rate (ORR, complete response [CR] + partial response
[PR]) in patients with relapsed or refractory HL
- to determine the safety profile of ruxolitinib in patients with relapsed or refractory
HL
Status | Completed |
Enrollment | 12 |
Est. completion date | May 17, 2019 |
Est. primary completion date | May 17, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility |
Inclusion Criteria: - relapsed or refractory HL - ECOG <= 2, - no major organ dysfunction - written informed consent Exclusion Criteria: - history of another primary malignancy = 2 years - female patients who are pregnant or breast feeding - patients with a known history of HIV seropositivity - chronic active hepatitis |
Country | Name | City | State |
---|---|---|---|
Germany | 1st Dept. of Medicine, Cologne University Hospital | Cologne |
Lead Sponsor | Collaborator |
---|---|
University of Cologne |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | overall response rate | 8 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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