Overview

This trial is active, not recruiting.

Condition advanced cancer
Treatment zio-101-c (darinaparsin)
Phase phase 1
Sponsor Ziopharm
Start date August 2007
End date June 2013
Trial size 23 participants
Trial identifier NCT00591422, SGC1001

Summary

The study of Dariniparsin (ZIO-101-C) in Advanced Solid Tumors and Non-Hodgkin's Lymphomas

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Endpoint classification safety/efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
zio-101-c (darinaparsin) ZIO-101-C
Capsule, Dose escalation study from 100 mg to 1000 mg (or Maximum Tolerated Dose). 3 times weekly (>36 hours between doses) for 3 weeks with 1 week rest.

Primary Outcomes

Measure
Toxicities
time frame: 6 months

Secondary Outcomes

Measure
pharmacokinetics
time frame: 6 months

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria 1. Patients with non-Hodgkin's Lymphomas that are refractory to standard therapies for their condition.(As of protocol amendment 6.0 dated 8/26/2009) 2. Men and women of ≥ 18 years of age. 3. ECOG performance score ≤ 2 (see Appendix 4). 4. Eligible subjects with lymphomas must have measurable disease as defined by the revised International Working Group response criteria (Appendix 7) 5. Life expectancy ≥ 12 weeks. 6. Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements, to be conducted <2 weeks prior to Baseline: - Creatinine ≤ 2X upper limit of normal (ULN) OR a calculated creatinine clearance ≥ 50 cc/min - Total bilirubin ≤ 2X ULN - Alanine transaminase (ALT) and aspartate transaminase (AST) ≤ 3X ULN - Granulocytes in peripheral blood ≥1 x 109/L, hemoglobin ≥8.5 g/dL, and platelets ≥50,000 /µL 7. Written informed consent in compliance with ZIOPHARM policies and the Human Investigation Review Committee (IEC/IRB) having jurisdiction over the site. Exclusion Criteria 1. New York Heart Association (NYHA) functional class ≥3 myocardial infarction (see Appendix 5) within 6 months. 2. Uncontrolled cardiac arrhythmia other than asymptomatic atrial fibrillation; a QTc ≥450 msec; or a ≥Grade 2 atrioventricular (AV) block or left bundle branch block (LBBB); or documented history of prolonged QTc. 3. Pregnant and/or lactating female. (Women of childbearing age must use effective contraception from Screening through the duration of Study participation.) 4. Uncontrolled systemic infection (documented with microbiological studies). 5. Metastatic brain or meningeal tumors. 6. Patients with seizure disorder requiring medication (such as anti-epileptics). 7. History of confusion or dementia or neurological condition that could mask a potential adverse response to Study Drug which may include transient ischemic attack, Parkinson's disease, thrombotic or hemorrhagic stroke, Alzheimers, and other neurological disorders. 8. Anticancer chemotherapy or immunotherapy during the study or within 4 weeks of Study entry (mitomycin C or nitrosureas should not be given within 6 weeks of Study entry). 9. Radiotherapy during study or within 3 weeks of Study entry. 10. Surgery within 4 weeks of start of Study Drug. 11. Investigational drug therapy outside of this trial during or within 4 weeks of Study entry. 12. History of invasive second primary malignancy diagnosed within the previous 3 years except for Stage I endometrial/cervical carcinoma or prostate carcinoma treated surgically, and non-melanoma skin cancer. 13. Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of Study results. 14. Any condition that is unstable or could jeopardize the safety of the patient and his/her compliance in the Study. 15. Arsenic allergy.

Additional Information

Official title Phase I Study of Oral Darinaparsin (ZIO-101-C) in Advanced Solid Tumors and Non-Hodgkin's Lymphomas
Trial information was received from ClinicalTrials.gov and was last updated in July 2012.
Information provided to ClinicalTrials.gov by Ziopharm.