Hodgkin's Lymphoma
Conditions
Brief summary
Defects in the apoptotic process can lead to the onset of cancer by allowing cells to grow unchecked when an oncogenic signal is present. Obatoclax is designed to restore apoptosis through inhibition of the Bcl-2 family of proteins, thereby reinstating the natural process of cell death that is often inhibited in cancer cells. This is a multi-center, open-label, Phase II study of single-agent obatoclax administered in 2-week cycles as a 24-hour infusion every 2 weeks at a fixed dose of 60 mg to patients with relapsed or refractory Hodgkin's Lymphoma. Infusions may be administered on an out-patient basis. No investigational or commercial agents or therapies other than those described in the protocol may be administered with the intent to treat the patient's malignancy. Supportive care measures including those directed at controlling symptoms resulting from Hodgkin's Lymphoma (blood products, growth factor, etc.) are allowed.
Interventions
60 mg q2wks
Sponsors
Gemin X
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Pathological confirmation of Hodgkin's Lymphoma. * Must have measurable disease. * Evidence of progressive disease following at least one prior line of combination therapy. * Must have failed, refused, or otherwise not a candidate for stem cell transplant. * Patient's must have normal organ function. * Willing to submit to blood sampling for planned PK and PD analyses. * Ability to understand and willingness to sign a written informed consent form.
Exclusion criteria
* No other agents or therapies administered with the intent to treat malignancy. * Patients with prior exposure to obatoclax. * Prior allogeneic stem cell transplant if evidence of graft versus host disease, or requirement for steroids or other immunosuppressive therapy. * Uncontrolled, intercurrent illness. * Pregnant women and women who are breast feeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determine the response rate to obatoclax and characterize the safety profile; Determine the steady-state pharmacokinetic parameters and pharmacodynamic response. | 4 weeks to 1 year |
Countries
United States
Outcome results
None listed