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Brain and Central Nervous System TumorsPhase 1NCT01158300

PTC299 in Treating Young Patients With Refractory or Recurrent Primary Central Nervous System Tumors

A Phase 1 study testing VEGF inhibitor PTC299 in people with Brain and Central Nervous System Tumors, run by Pediatric Brain Tumor Consortium at 8 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

RATIONALE: PTC299 may stop the growth of tumor cells by blocking blood flow to the tumor. PURPOSE: This phase I trial is studying the side effects and the best dose of PTC299 in treating young patients with recurrent or refractory primary central nervous system tumors. Read more about this study

Who is it for?
Ages 3 to 21 years
Conditions the study is for
Brain and Central Nervous System Tumors
What is being tested?
VEGF inhibitor PTC299
Type of treatment
Pill or oral medicine
How many people
28 participants
Where
8 sitesUnited States
Study dates
Nov 2010to Jan 2015
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 to 21 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

DISEASE CHARACTERISTICS:

  • Histologically confirmed diagnosis of primary central nervous system (CNS) malignancy at time of diagnosis or recurrence
  • Histology verification not required for intrinsic brain stem tumors and optic pathway gliomas
  • Must have radiographic evidence of progression
  • Recurrent, progressive, or refractory disease to standard therapy and for which there is no known curative therapy

PATIENT CHARACTERISTICS:

  • Karnofsky performance status (PS) 50-100% (patients > 16 years of age) OR Lansky PS 50-100% (patients ≤ 16 years of age)
  • Body weight ≥ 15 kg and ≤ 100 kg
  • Patients with neurological deficits allowed provided they are stable for ≥ 1 week
  • Able to swallow capsules
  • ANC ≥ 1,000/μL (unsupported)
  • Platelet count ≥ 100,000/μL (unsupported)
  • Hemoglobin ≥ 8 g/dL (may be supported)
  • Creatinine clearance or radioisotope glomerular filtration rate (GFR) ≥ 70 mL/min/1.73 m^2 OR serum creatinine normal based on age as follows:
  • 0.8 mg/dL (≤ 5 years of age)
  • 1.0 mg/dL (> 5 to ≤ 10 years of age)
  • 1.2 mg/dL (> 10 to ≤ 15 years of age)
  • 1.5 mg/dL (> 15 years of age)
  • Urine protein/creatinine ratio < 1.0
  • Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
  • ALT and AST ≤ 2.5 times ULN
  • Albumin ≥ 2.5 g/dL
  • PT and activated PTT ≤ 1.2 times ULN
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No clinically significant unrelated systemic illness that would compromise the patient's ability to tolerate protocol therapy, or would likely interfere with the study procedures or results, including any of the following:
  • Serious infections including ongoing systemic bacterial, fungal, or viral infection
  • Significant cardiac, pulmonary, hepatic, or other organ dysfunction
  • Willing and able to comply with schedule visits, drug administration plan, laboratory tests, including pharmacokinetic and pharmacodynamic assessments, or other study procedures
  • No known coagulopathy or bleeding diathesis
  • No known history of drug-induced liver injury
  • No CNS, pulmonary, gastrointestinal, or urinary bleeding within the past month
  • No uncontrolled systemic hypertension (systolic BP or diastolic BP > 95% percentile for age)
  • No alcohol or drug addiction
  • Able to tolerate periodic MRI scans and gadolinium contrast

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • Recovered from the acute toxic of all prior therapy (excluding alopecia and neurotoxicity)
  • At least 3 weeks since prior myelosuppressive anticancer chemotherapy (6 weeks for nitrosourea)
  • At least 14 days since prior investigational or biological agent
  • At least 3 half-lives since prior biological agents that have a prolonged half-life
  • At least 3 half-lives since prior monoclonal antibody
  • At least 2 weeks since prior local palliative radiotherapy
  • At least 6 weeks since prior total-body irradiation, craniospinal radiotherapy, or radiotherapy to ≥ 50% of the pelvis
  • At least 90 days since prior allogeneic bone marrow transplantation
  • No active graft-versus-host disease
  • Concurrent dexamethasone or other corticosteroids allowed provided dose is stable for ≥ 7 days
  • At least 1 week since prior colony-forming growth factors (e.g., filgrastim, sargramostim, erythropoietin)
  • At least 14 days since long-acting colony-forming growth factor formulations (e.g., pegfilgrastim)
  • More than 4 weeks since prior major surgical procedures
  • More than 2 weeks since prior intermediate surgical procedures
  • More than 7 days since minor surgical procedures
  • No other concurrent anticancer or investigational drug therapy

Trial locations and contacts

8 sites in 1 country.

8 sites in 1 country

United States8 sites
  • Children's Memorial Hospital - Chicago

    Chicago, Illinois, 60614

  • Duke Comprehensive Cancer Center

    Durham, North Carolina, 27710

  • Texas Children's Cancer Center and Hematology Service at Texas Children's Hospital

    Houston, Texas, 77030-2399

  • St. Jude Children's Research Hospital

    Memphis, Tennessee, 38105

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania, 19104-4318

  • Children's Hospital of Pittsburgh

    Pittsburgh, Pennsylvania, 15213

  • UCSF Cancer Center and Cancer Research Institute

    San Francisco, California, 94143-0128

  • Children's National Medical Center

    Washington D.C., District of Columbia, 20010-2970

Other trials in United States

About this study

Official title: Phase I and Pharmacokinetic Trial of PTC299 in Pediatric Patients With Refractory or Recurrent CNS Tumors

RATIONALE: PTC299 may stop the growth of tumor cells by blocking blood flow to the tumor.

PURPOSE: This phase I trial is studying the side effects and the best dose of PTC299 in treating young patients with recurrent or refractory primary central nervous system tumors.

Read the detailed description

OBJECTIVES:

Primary

  • To estimate the maximum-tolerated dose and the recommended phase II dose of VEGF inhibitor PTC299 (PTC299) in pediatric patients with recurrent or progressive primary central nervous system (CNS) tumors.
  • To evaluate and characterize the adverse events associated with this regimen in these patients.
  • To evaluate and characterize the pharmacokinetics and pharmacodynamics of this regimen in these patients.

Secondary

  • To investigate the relationships between PTC299 plasma exposure and other outcomes measures.
  • To evaluate the antitumor activity of this regimen in these patients.
  • To evaluate changes in angiogenic and inflammatory markers in the blood and the relationship between these changes and other outcome measures.
  • To obtain preliminary evidence of biologic activity of PTC299 by using magnetic resonance diffusion to assess tumor cellularity.

OUTLINE: This is a multicenter, dose-escalation study.

Patients receive oral VEGF inhibitor PTC299 twice or thrice daily. Treatment repeats every 28 days for up to 12 courses in the absence of disease progression or unacceptable toxicity.

Blood samples are collected at baseline and periodically during study for pharmacokinetic and pharmacodynamic studies by ELISA.

After completion of study therapy, patients are followed up for 30 days.

Being tested
VEGF inhibitor PTC299
Keywords
recurrent childhood malignant germ cell tumor, recurrent childhood brain stem glioma, recurrent childhood brain tumor, recurrent childhood central nervous system embryonal tumor, recurrent childhood cerebellar astrocytoma, recurrent childhood cerebral astrocytoma, recurrent childhood ependymoma, recurrent childhood medulloblastoma, recurrent childhood pineoblastoma, recurrent childhood rhabdomyosarcoma, recurrent childhood spinal cord neoplasm, recurrent childhood subependymal giant cell astrocytoma, recurrent childhood visual pathway and hypothalamic glioma, recurrent childhood visual pathway glioma, childhood central nervous system choriocarcinoma, childhood central nervous system germ cell tumor, childhood central nervous system germinoma, childhood central nervous system mixed germ cell tumor, childhood central nervous system teratoma, childhood central nervous system yolk sac tumor
Medical subject headings
Central Nervous System Neoplasms, Astrocytoma, Familial ependymoma, Medulloblastoma, Spinal Cord Neoplasms, Optic Nerve Glioma, Meningioma, Oligodendroglioma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • VEGF inhibitor PTC299Drug

    This is a dose escalation study. Study participants will receive .6 or 1.2 mg/kg orally twice daily or 1.2, 1.5, or 2.0 mg/kg orally three times daily for four consecutive weeks (a course). In the absence of unacceptable toxicity or disease progression, treatment may continue for up to 12 courses (approximately one year)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Maximum-tolerated dose

    Measured: First four weeks of treatment

  2. Adverse events

    Measured: From the first day of treatment until 30 days after the last dose

Secondary outcomes (3)
  1. Percentage of study participants with complete response or partial response to the study treatment

    Brain images to assess partial or complete response are performed every 8 weeks after the first dose of the study drug.

    Measured: Every 8 weeks

  2. Pharmacokinetics

    Blood samples from study participants will be collected on day 1 and day 28 of course 1 for standard full pharmacokinetic studies.

    Measured: Day 1 and day 28 of course 1

  3. Change from baseline in blood angiogenic markers and cytokines at discontinuation or completion of treatment

    Blood samples will be collected and analyzed on Day 1 of pre-AM dosing at baseline and at the discontinuation or completion of treatment. Changes from baseline in blood angiogenic markers and cytokines (VEGF-A, VEGF-C, VEGF-D, PlGF, VEGFR-1, VEGFR-2, IL-6, and IL-8) will be assessed.

    Measured: Before the first dose of drug on day 1 of course 1 and at the discontinuation or completion of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Jul 2010 (estimated)
  2. Study startNov 2010
  3. Primary completionJan 2015
  4. Study completionJan 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
28 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01158300
Sponsor's protocol ID
CDR0000680634
Other IDs
U01CA081457, PBTC-031, PTC299-ONC-010-PBT
Status last verified
May 2015
First submitted
7 Jul 2010
Last updated
4 May 2015
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing VEGF inhibitor PTC299 in people with Brain and Central Nervous System Tumors, run by Pediatric Brain Tumor Consortium at 8 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 May 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Maximum-tolerated dose (time frame: First four weeks of treatment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 May 2015.

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