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A Study of JNJ-40346527 in Patients With Relapsed or Refractory Hodgkin Lymphoma
Not Recruiting
Trial ID: NCT01572519
Purpose
The purpose of this study is to determine the safety, pharmacokinetics, and preliminary
efficacy information of JNJ-40346527 in patients with relapsed or refractory Hodgkin
lymphoma.
Official Title
An Open-label, Multicenter, Phase 1/2 Study of JNJ-40346527, an FMS Inhibitor, in Subjects With Relapsed or Refractory Hodgkin Lymphoma
Stanford Investigator(s)
Lauren Maeda
Clinical Associate Professor, Medicine - Oncology
Eligibility
Inclusion Criteria:
- Patients with histopathologically confirmed initial diagnosis of Hodgkin lymphoma and who
have disease that has relapsed or is refractory that is progressing or active and requires
treatment after at least 1 appropriate therapy
Exclusion Criteria:
- Known brain metastases or leptomeningeal disease
- Other malignancy within past 5 years
- Has any condition that, in the opinion of the investigator, would make study
participation not be in the best interest (eg, compromise the well-being) of the
patient or that could prevent, limit, or confound the protocol-specified assessments
- QTc prolongation at screening or other factors that increase the risk of QT
prolongation such as diagnosis or family history of long-QT syndrome, diagnosed or
suspected congenital long QT syndrome, or concomitant use of medication that can
prolong the QT interval
- Taking CYP3A4 substrate drugs with a narrow therapeutic index (eg, alfentanil,
astemizole, sirolimus, tacrolimus, terfenadine)
Intervention(s):
drug: Phase 1, Cohort 1
drug: Phase 1, Cohort 2
drug: Phase 1, Cohort 3
drug: Phase 1, Cohort 4
drug: Phase 2
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Sarah Daadi
650-725-6456