Adult Study: ABT-414 Alone or ABT-414 Plus Temozolomide vs. Lomustine or Temozolomide for Recurrent Glioblastoma Pediatric Study: Evaluation of ABT-414 in Children With High Grade Gliomas
DFCI Protocol ID: 16-543
This study is to evaluate the efficacy and safety of ABT-414 alone or with temozolomide versus temozolomide or lomustine alone in participants with recurrent glioblastoma multiforme. The study includes a Pediatric sub-study to evaluate safety, tolerability and pharmacokinetics of ABT-414 in a pediatric population. Adult enrollment has been completed and the study is now only recruiting for pediatric participants.
Children's Hospital Boston, Dana-Farber Cancer Institute
Dana-Farber Cancer Institute:
Childrens Hospital Pediatric Clinical Translation Investigation Program CTIP, email@example.com
Adult participants (greater than or equal to 18 years old):
- Histologically confirmed de novo (primary) Glioblastoma Multiforme with unequivocal
tumor progression or recurrence.
- In case of testing at the time of first progression: either at least 3 months after
the end of radiotherapy or have tumor progression that is clearly outside the
radiation field or have tumor progression unequivocally proven by surgery/biopsy
- Absence of any psychological, familial, sociological or geographical factors
potentially hampering compliance with the study protocol and follow-up schedule; such
conditions should be assessed with the patient before registration in the trial.
- Availability of adequate biological material (formalin-fixed paraffin embedded [FFPE]
tumor) for central testing of Epithelial Growth Factor Receptor (EGFR) amplification
- Presence of EGFR amplification confirmed by central assessment; participants with
undetermined EGFR status are excluded
- World Health Organization (WHO) Performance status 0 - 2
- No more than one line of chemotherapy (concurrent and adjuvant Temozolomide based
chemotherapy including in combination with another investigational agent is
considered one line of chemotherapy). Chemotherapy must have been completed at least
4 weeks prior to randomization.
- Post surgery MRI within 48 hours following surgery, however an MRI scan has to be
done within 2 weeks prior to randomization.
- Surgery completed at least 2 weeks before randomization and patients should have
fully recovered as assessed by investigators.
Pediatric sub-study participants (less than 18 years old):
- The study will only include patients under 3 years of age when results of a juvenile
repeated mouse toxicity study become available and are favorable to support use in
patients aged under 3 years.
- Histologically proven high grade glioma (HGG: WHO grade III glioma [e.g anaplastic
astrocytoma, anaplastic oligodendroglioma, anaplastic oligoastrocytoma], grade IV
glioma [e.g glioblastoma, gliosarcoma] or diffuse intrinsic pontine glioma [DIPG]).
- Must either have recurrent/progressive tumor or, if newly diagnosed, have completed
any planned radiation therapy at least 4 weeks prior to first dose of ABT-414.
- The tumor tissue must have been determined to have EGFR amplification, (by local or
other testing service).
- availability of adequate biological material for retrospective confirmatory central
testing of EGFR amplification
- Participant has sufficiently recovered from previous therapy. The investigator
believes that benefit of treating the pediatric subject with ABT-414 outweighs the
expected risks and that this treatment is in the best interests of the pediatric
Adult population (greater than or equal to 18 years old):
- Prior treatment with nitrosoureas
- Prior treatment with bevacizumab
- Previous exposure to Epithelial Growth Factor Receptor (EGFR) targeted agents,
including EGFRvIII targeting agents
- Prior discontinuation of temozolomide chemotherapy for toxicity reasons
- Prior Radiation Therapy (RT) with a dose over 65 Gy, stereotactic radiosurgery or
brachytherapy unless the recurrence is histologically proven
- Previous other malignancies, except for any previous malignancy which was treated
with curative intent more than 5 years prior to randomization, and except for
adequately controlled limited basal cell carcinoma of the skin, squamous carcinoma of
the skin or carcinoma in situ of the cervix
- Women of childbearing potential must have a negative serum or urine pregnancy test
(minimum sensitivity 25 IU/L or equivalent units of HCG) within 72 hours prior to
- No history of wheat allergies and Coeliac disease.
- No EIAED, patients who require anti-convulsant therapy must be taking non-enzyme
inducing antiepileptic drugs (non-EIAED). Patients previously on EIAED must be fully
switched to non-EIAED at least 2 weeks prior to randomization.
Pediatric sub-study (less than 18 years old):
- (For recurrent disease) No prior RT with a dose over 65Gy to the brain, stereotactic
radiosurgery or brachytherapy unless the recurrence is histologically proven
- No current or recent (within 4 weeks or 5 half-lives (whichever is shorter) before
enrollment) treatment with another investigational drug
- Female participants of childbearing potential must have a negative serum or urine
pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 72
hours prior to randomization.