Phase I Trial of ZIO-101 in Patients With Solid Tumors
N/A
N/A
Both
Solid Tumors
Trial Information
Phase I Trial of ZIO-101 in Patients With Solid Tumors
ZIO-101 is a drug that may change cancerous cells into healthy (benign) cells. It is also
designed to cause cancer cells to destroy themselves; a term called apoptosis.
Before you can start treatment on this study, you will have what are called "screening
tests" no more than one week before starting the study. These tests will help the doctor
decide if you are eligible to take part in the study. You will have a complete medical
history and physical exam, including measurements of your weight, blood pressure, pulse, and
temperature. You will also be asked what other medicines you are taking and about your
general well-being. You will have an electrocardiogram (ECG - a test to measure the
electrical activity of the heart). Blood (about 2 1/2 tablespoons) will be drawn. A sample
of urine will be also be collected and tested to see if your kidneys are working correctly.
Women who are able to have children must have a negative urine pregnancy test.
To see the current condition of your tumor, additional tests may need to be performed if
they have not already been done recently. These tests may include a chest x-ray, a CT scan
(imaging computer pictures of your body), a bone scan (an imaging test of your bones with a
contrast material), or an MRI (a detailed imaging scan of certain areas of your body).
If you are found to be eligible to take part in this study, you will begin treatment with
ZIO-101. Immediately before being treated with ZIO-101 on Day 0, you will have another
physical exam and you will be asked about any medicines you are taking and how you are
feeling. You will also be asked a series of questions which will assess your mental health.
This is called a mini-mental status exam and will take approximately 10 minutes to complete.
The blood tests may need to be repeated along with the ECG and the urine test. In addition,
a small blood sample (about 10 teaspoons) must be taken immediately before the injection of
ZIO-101. This blood will be used to help in the measurement of drug levels in the blood.
These are called pharmacokinetic (PK) tests. This blood sample will also be used to measure
arsenic levels in your blood.
ZIO-101 will be injected into your vein over 60 minutes in the clinical translational
research center of UTMDACC. This drug must be given through a special IV called a central
line catheter so that it does not damage your surrounding tissue. You will have to sign a
separate consent document before placement of a catheter can be performed. Special care will
be taken to be sure the drug does not leak into surrounding tissue. The use of anti-nausea
and other supportive care medications may be given during the infusion.
Following the injection, you will have 6 samples of blood taken for PK tests at half an hour
and 1, 2, 4, 8, and 12 hours after finishing the treatment.
For the next 4 days at about the same time as your first infusion, you will be prepared for
treatment with ZIO-101. Before each injection, you will be asked how you feel, an ECG will
be performed, and a small sample of blood (about 2 teaspoons) will be drawn for PK tests.
The Day 1-4 infusions will also each take about 1 hour. In total you will receive 5 daily
injections of ZIO-101. On Day 4 at the end of the infusion, another sample of blood will be
drawn (about 5 teaspoons) to measure arsenic levels in your blood.
Your next visit will be Week 2 and at the start of this visit, a blood sample (about 2
teaspoons) will be drawn for PK tests, and you will be asked how you feel. At Week 3,
another blood sample (about 7 teaspoons) will be drawn for PK tests, and to measure arsenic
levels in your blood, and you will again be asked how you feel.
At Week 4, a new cycle begins. Immediately before being treated with ZIO-101, you will have
a physical examination and you will take a mini-mental status examination; you will be asked
about any medicines you are taking and how you are feeling. The blood tests will be
repeated along with the ECG and the routine urine test. In addition, tests to measure your
tumor will be repeated.
This study is trying to find the best dose of ZIO-101. At first, 3 patients will be
assigned to the first dose level. They will be followed to evaluate their side effects for a
period of 4 weeks before 3 more patients are enrolled. If none of the patients develop
serious side effects, the dose escalation will continue. If 1 of the 3 patients in a
particular dose level develops significant side effects, 3 more patients will be enrolled at
that level. If 2 or more of the 6 patients develop serious side effects, then the escalation
will finish and all future patients on this study will be treated at a lower dose level
(half way between this level and the previous one).
You may receive up to 6 cycles of treatment. You may be taken off study early if your
disease gets worse or intolerable side effects occur. Once you go off study, you will have
an end of study visit. During this visit, you will have a physical exam, a mini-mental
status exam and blood (about 3 teaspoons) will be drawn for routine tests.
This is an investigational study. ZIO-101 has been authorized by the FDA for use in
research only. ZIO-101 will be provided free of charge during the study. Also, any tests
or procedures that are being done solely for the purpose of this research study will be
provided free of charge. Up to 50 patients will take part in this multicenter study. All
will be enrolled at M. D. Anderson.
Inclusion Criteria:
1. Patients with histological confirmation solid malignancy refractory to conventional
standard therapies for their condition.
2. Eligible subjects MUST have at least one measurable lesion as defined by RECIST
guidelines. If the measurable disease is restricted to a solitary lesion, its
neoplastic nature should be confirmed by cytology/histology. Measurable lesions MUST
not have been in a previously irradiated field or injected with biological agents.
3. Pediatric patients will be eligible at the discretion of the primary investigator.
4. ECOG performance status score
5. Women of child-bearing potential (i.e., women who are pre-menopausal or not
surgically sterile) must use acceptable contraceptive methods (abstinence,
intrauterine device [IUD], oral contraceptive or double barrier device), and must
have a negative blood or urine pregnancy test within 1 week before beginning
treatment. Sexually active men must also use acceptable contraceptive methods.
6. Patients must provide written informed consent prior to treatment.
7. At least four weeks from completion of prior therapy to day 1 of study drug.
8. Baseline toxicity assessment less than or equal to grade 1 except treatment induced
alopecia (NCI Common Terminology Criteria for Adverse Events [CTCAE] version 3.0).
9. Evidence of adequate multi-organ functional status as reflected by the following
clinical laboratory values: - Serum creatinine a calculated creatinine clearance upper normal limit. - Alanine aminotransferase (ALT), OR aspartate aminotransferase
(AST)
10. Granulocytes in peripheral blood greater than or equal to 1 x 10(9) per liter,
hemoglobin greater than or equal to 8.5 g/dL, and platelets greater than or equal to
50,000 cells/microL.
Exclusion Criteria:
1. Uncontrolled systemic infection (documented with microbiological studies).
2. Active heart disease as defined by an acute myocardial infarction within the previous
6 months before starting therapy, stable or unstable angina, clinically significant
arrhythmia requiring medical management, OR New York Heart Association Classification
of Functional Activities. Class 3: Patient has marked limitation in activities due to
symptoms, even during less-than-ordinary activity and is comfortable only at rest OR
Class 4: Severe limitations. Patient experiences symptoms even while at rest.
3. Concomitant therapy for solid cancer.
4. Pregnant subjects and those who are breast-feeding.
5. History of an 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.
6. Documented personal or family history of prolonged QT syndrome.
7. 12 lead electrocardiogram with a corrected QT interval >/= 460 milliseconds.
8. History of confusion or dementia.
9. History of seizure disorder.
Type of Study:
Interventional
Study Design:
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Outcome Measure:
Maximum tolerated dose (MTD)
Outcome Time Frame:
Daily for 5 consecutive days repeated every 4 weeks for 1 cycle; evaluation of 4-6 dose escalations to determine an MTD
Safety Issue:
Yes
Principal Investigator
Razelle Kurzrock, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
M.D. Anderson Cancer Center
Authority:
United States: Food and Drug Administration
Study ID:
2004-0909
NCT ID:
NCT00509782
Start Date:
May 2005
Completion Date:
April 2008
Related Keywords:
- Solid Tumors
- Solid Tumors
- Anti-Tumor Effects
- ZIO-101
- Neoplasms
Name | Location |
|---|---|
| U.T.M.D. Anderson Cancer Center | Houston, Texas 77030 |
