A Phase-II Trial of ZIO 101 in Advanced Hepatocellular Carcinoma
NCT ID: NCT00423306
Last Updated: 2013-11-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE2
15 participants
INTERVENTIONAL
2007-01-31
2013-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Single Arm
Darinaparsin
420 mg/m2 of Darinaparsin given twice weekly for three weeks, followed by one week of rest, for up to 6 months
Interventions
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Darinaparsin
420 mg/m2 of Darinaparsin given twice weekly for three weeks, followed by one week of rest, for up to 6 months
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Male or female patients ≥ 18 years of age
3. Patients who have a life expectancy of at least 12 weeks
4. Patients who have at least one uni-dimensional measurable lesion by CT-scan or MRI according to Response Evaluation Criteria in Solid Tumors (RECIST).
5. Patients who have an Eastern Co-operative Oncology Group (ECOG) performance status of 0 - 2 (see Appendix 4).
6. Patients who have received local therapy, such as surgery, radiation therapy, hepatic arterial embolization, chemo-embolization, radio-frequency ablation or cryo-ablation are eligible, provided that they either have a target lesion which has not been subjected to local therapy and/or the target lesion(s) within the field of the local therapy has shown an increase of ≥ 25% in the size. Furthermore, the local therapy applied to target or non-target lesions needs to have been completed at least 8 weeks prior to study inclusion. Lesions treated with external beam radiation therapy are not acceptable as target lesions, unless they fulfil the conditions described above.
7. No more than one prior chemotherapy based regimen is allowed. Patients can receive up to two regimes where target therapies have been used (washout)
8. Cirrhotic status of Child-Pugh Class A or B only (Appendix 5).
9. Adequate hepatic function at screening as assessed by the following:
* Platelet count ≥ 60 x 109/L
* Hemoglobin ≥ 8.5 g/dl
* Total bilirubin ≤ 3 mg/dl
* ALT and AST ≤ 5 x upper limit of normal
* Serum creatinine ≤ 2.0 x the upper limit of normal
* PT-INR ≤ 2.3 or PT ≤ 6 seconds above control
10. Patients who give written informed consent prior to any study specific screening procedures with the understanding that the patient has the right to withdraw from the study at any time, without prejudice.
Exclusion Criteria
2. Congestive heart failure \> NYHA Class II
3. Cardiac arrhythmias requiring anti-arrythmics (excluding beta blockers or digoxin for chronic stable atrial fibrillation) or QTc greater than 450 msec.
4. Active coronary artery disease or cardiac ischemia
5. Active clinically serious bacterial, viral or fungal infections (\> grade 2 NCI-CTCAE, Version 3)
6. Known history of human immunodeficiency virus (HIV) infection for less than 2 years or uncontrolled disease on antiretroviral medication
7. Metastatic brain or meningeal tumors
8. Patients with seizure disorder requiring medication (such as anti-epileptics)
9. History of confusion or dementia or neurological condition that could mask a potential adverse response to the study drug (or something along these lines)
10. History of organ allograft
11. Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
12. Known or suspected allergy to the investigational agent or any agent given in association with this trial
13. Any condition that is unstable or which could jeopardize the safety of the patient and his/her compliance in the study
14. Pregnant or breast-feeding patients. Women of childbearing potential must have a negative pregnancy test performed within 14 days prior to the start of study drug. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial
18 Years
ALL
No
Sponsors
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Alaunos Therapeutics
INDUSTRY
Responsible Party
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Locations
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Miami, Florida, United States
Atlanta, Georgia, United States
Boston, Massachusetts, United States
Kansas City, Missouri, United States
New York, New York, United States
Seattle, Washington, United States
Countries
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Other Identifiers
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SGL2005
Identifier Type: -
Identifier Source: org_study_id