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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date April 2020
Source University of Cologne
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ruxolitinib


Locations

Country Name City State
Germany 1st Dept. of Medicine, Cologne University Hospital Cologne

Sponsors (1)

Lead Sponsor Collaborator
University of Cologne

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary overall response rate 8 weeks
See also
  Status Clinical Trial Phase
Completed NCT03229278 - Trigriluzole With Nivolumab and Pembrolizumab in Treating Patients With Metastatic or Unresectable Solid Malignancies or Lymphoma Phase 1

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