View Clinical Trial (Medical Research Study)
A Phase I Pharmacokinetic and Safety Study in Children With Recurrent or Refractory Medulloblastoma to Identify a Pharmacokinetic Based Dose for GDC-0449
| City: |
|
Durham |
| State: |
|
North Carolina |
| Zip Code: |
|
27710 |
| Conditions: |
|
Recurrent Childhood Medulloblastoma |
| Purpose: |
|
This phase I trial is studying the side effects and best dose of GDC-0449 in treating young
patients with medulloblastoma that is recurrent or did not respond to previous treatment.
GDC-0449 may be effective in treating young patients with medulloblastoma
|
| Study Summary: |
|
PRIMARY OBJECTIVE:
I. To investigate the safety and pharmacokinetics of a daily dose of hedgehog antagonist
GDC-0449 using the available formulation in pediatric patients with recurrent or refractory
medulloblastoma.
SECONDARY OBJECTIVES:
I. To document and describe toxicities associated with this drug in these patients.
II. To characterize the pharmacokinetics of this drug in these patients. III. To document
preliminary antitumor activity of this drug in these patients. IV. To document pathologic
and genomic methods to identify CNS tumors with activation of the PTCH/SHH pathway.
OUTLINE: This is a multicenter study.
Patients receive oral hedgehog antagonist GDC-0449 once daily on days 1 and 4-28 in course 1
and on days 1-28 in all subsequent courses. Treatment repeats every 28 days for up to 26
courses in the absence of disease progression or unacceptable toxicity.
Blood samples are collected periodically for pharmacokinetic studies. Archival tumor tissue
samples are collected and analyzed for the expression of genes that activate the SHH (e.g.,
Gli1, Gli2, SFRP1, ATOH1, and PTCH2) or WNT (e.g., DKK2 and DKK4) cell signal pathways by in
situ hybridization and reverse transcriptase real time-PCR.
After completion of study therapy, patients are followed for 90 days.
|
| Criteria: |
|
Inclusion Criteria:
- Histologically confirmed medulloblastoma, including posterior fossa primitive
neuroectodermal tumor (PNET)
- Recurrent, progressive, or refractory to standard therapy
- No known curative therapy exists
- Neurological deficits allowed provided they are stable for ≥ 1 week prior to study
entry
- No atypical teratoid/rhabdoid tumor or supratentorial PNET
- Karnofsky performance status (PS) 60-100% (for patients > 16 years of age) OR Lansky
PS 60-100% (for patients ≤ 16 years of age)
- ANC ≥ 1,000/μL*
- Platelet count ≥ 100,000/μL (transfusion independent)*
- Hemoglobin ≥ 8.0 g/dL (RBC transfusion allowed)*
- Creatinine clearance or radioisotope GFR ≥ 70 mL/min OR serum creatinine based on age
as follows:
- ≤ 0.8 mg/dL (for patients ≤ 5 years of age)
- ≤ 1.0 mg/dL (for patients 6 to 10 years of age)
- ≤ 1.2 mg/dL (for patients 11 to 15 years of age)
- ≤ 1.5 mg/dL (for patients > 15 years of age)
- Total bilirubin ≤ 1.5 times upper limit of normal (ULN) for age
- ALT/AST ≤ 2.5 times ULN for age
- Serum albumin ≥ 2.5 g/dL
- Not pregnant or nursing
- Negative pregnancy test
- Fertile female patients must use 2 effective methods of contraception during and for
12 months following study treatment
- Fertile male patients must use effective barrier contraception during and for 12
months following study treatment
- Body surface area > 0.67 m^2 and ≤ 2.5 m^2
- Able to swallow capsules
- No malabsorption syndrome or other condition that would interfere with enteral
absorption
- No history of congestive heart failure
- No history of ventricular arrhythmia requiring medication
- No uncontrolled hypocalcemia, hypomagnesemia, hyponatremia, or hypokalemia, defined
as less than the lower limit of normal despite adequate electrolyte supplementation
- No clinically important history of liver disease, including viral hepatitis or
cirrhosis
- No concurrent clinically significant unrelated systemic illness (e.g., serious
infection) or significant cardiac, pulmonary, hepatic, or other organ dysfunction
that would compromise the patient's ability to tolerate study treatment or would
likely interfere with study procedures or results
- NOTE: * In the absence of bone marrow involvement
- Recovered from prior treatment-related toxicity
- At least 3 months since prior craniospinal radiotherapy (at doses ≥ 23 Gy)
- At least 8 weeks since prior local radiotherapy to primary tumor
- At least 2 weeks since prior focal radiotherapy to symptomatic metastatic sites
- More than 4 weeks since prior myelosuppressive chemotherapy or immunotherapy (6 weeks
for nitrosoureas)
- More than 1 week since prior colony-stimulating factors (e.g., filgrastim [G-CSF],
sargramostim [GM-CSF], or erythropoietin)
- No other concurrent anticancer or investigational drug therapy
- Concurrent dexamethasone allowed provided dosage is stable or decreasing for ≥ 1 week
prior to study entry
|
| NCT ID: |
|
NCT00822458 |
| Primary Contact: |
|
Principal Investigator
Amar Gajjar
Pediatric Brain Tumor Consortium
|
| Backup Contact: |
|
N/A |
| Location Contact: |
|
Durham, North Carolina 27710
United States
Sridharan Gururangan
Phone: 919-668-6288
Email: gurur002@mc.duke.edu
Site Status: Recruiting |
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
May 20, 2013 |
| Modifications to this listing: |
|
Only selected fields are shown, please use the link
below to view all information about this clinical trial. |
|
Click to view Full Listing
|