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Safety and Efficacy of Obatoclax Mesylate (GX15-070MS) in the Treatment of Hodgkin's Lymphoma

Primary Purpose

Hodgkin's Lymphoma

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Obatoclax mesylate (GX15-070MS)
Sponsored by
Gemin X
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hodgkin's Lymphoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • MD Anderson Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Obatoclax Mesylate

Arm Description

Obatoclax Mesylate 60mg

Outcomes

Primary Outcome Measures

Determine the response rate to obatoclax and characterize the safety profile; Determine the steady-state pharmacokinetic parameters and pharmacodynamic response.

Secondary Outcome Measures

Full Information

First Posted
August 2, 2006
Last Updated
August 3, 2012
Sponsor
Gemin X
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1. Study Identification

Unique Protocol Identification Number
NCT00359892
Brief Title
Safety and Efficacy of Obatoclax Mesylate (GX15-070MS) in the Treatment of Hodgkin's Lymphoma
Official Title
A Multi-Center, Open-Label Phase II Study of Single-Agent GX15-070MS Administered as a 24-Hour Infusion Every 2 Weeks to Patients With Relapsed or Refractory Hodgkin's Lymphoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
November 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Gemin X

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hodgkin's Lymphoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Obatoclax Mesylate
Arm Type
Experimental
Arm Description
Obatoclax Mesylate 60mg
Intervention Type
Drug
Intervention Name(s)
Obatoclax mesylate (GX15-070MS)
Intervention Description
60 mg q2wks
Primary Outcome Measure Information:
Title
Determine the response rate to obatoclax and characterize the safety profile; Determine the steady-state pharmacokinetic parameters and pharmacodynamic response.
Time Frame
4 weeks to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Viallet, MD
Organizational Affiliation
Gemin X, Inc.
Official's Role
Study Director
Facility Information:
Facility Name
MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22383790
Citation
Oki Y, Copeland A, Hagemeister F, Fayad LE, Fanale M, Romaguera J, Younes A. Experience with obatoclax mesylate (GX15-070), a small molecule pan-Bcl-2 family antagonist in patients with relapsed or refractory classical Hodgkin lymphoma. Blood. 2012 Mar 1;119(9):2171-2. doi: 10.1182/blood-2011-11-391037. No abstract available.
Results Reference
derived

Learn more about this trial

Safety and Efficacy of Obatoclax Mesylate (GX15-070MS) in the Treatment of Hodgkin's Lymphoma

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