Study Of NOVOTTF-200A In Bevacizumab-Naive Subjects With Recurrent Grade III Malignant Astrocytoma

Completed · Not applicable

Conditions studied: Astrocytoma, Grade III

In brief

This is a Phase 2 study in subjects with WHO Grade III Anaplastic Astrocytoma (G3 astrocytoma) who had progressive disease during first or second line treatment and who have not previously received any BEV or any experimental agents.

Key facts

Study ID

NCT03450850

Run by

Daniela A. Bota

People needed

1

Starts

2020-05-21

Expected to finish

2025-08-07

Last updated by the study team

2026-02-17

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Understand and voluntarily sign and date an informed consent document before any study related assessments/procedures are conducted.
• Males and females of age ≥18 years at the time of the signing of the informed consent document.
• All subjects must have histologic evidence of G3 MG and radiographic evidence of recurrence or disease progression (defined as either a greater than 25% increase in the largest bi-dimensional product of enhancement, a new enhancing lesion or a significant increase in T2 FLAIR).
• Subjects with archival tumor tissue suitable for genetic testing must give permission to access and test the tissue; subjects without archival tumor tissue are eligible.
• No prior treatment with BEV or any anti-angiogenesis agents.
• At least 4 weeks from surgical resection and 12 weeks from end of radiotherapy prior to enrollment in this study, unless relapse is confirmed by tumor biopsy or new lesion outside of radiation field, or if there are two MRIs confirming progressive disease that are 8 weeks apart.
• All AEs resulting from prior chemotherapy, surgery or radiotherapy must have resolved to NCI-CTCAE (v. 4.03) Grade ≤1 (except for laboratory parameters outlined below).
• Laboratory results within 7 days prior to NOVOTTF-200A administration (transfusions and/or growth factor support may be used at the discretion of the Investigator during Screening):
• Hemoglobin ≥9 g/dL.
• Absolute neutrophil count (ANC) ≥1.5 × 109/L.
• Platelet count ≥100 × 109/L.
• Serum bilirubin ≤1.5 × upper limit of normal (ULN) or ≤3 × ULN if Gilbert's disease is documented.
• Aspartate transaminase (AST) ≤ 2.5 ULN.
• Serum creatinine ≤1.5 × ULN.
• Karnofsky Performance Status (KPS) score ≥70%.
• Willing and able to adhere to the study visit schedule and other protocol requirements.

You may not qualify if…

• The presence of any of the following will exclude a subject from enrollment:
• The presence of 1p19q LOH which is diagnostic for anaplastic oligodendroglioma (AO).
• Co-medication that may interfere with study results, e.g., immunosuppressive agents other than corticosteroids. (Steroid therapy for control of cerebral edema is allowed at the discretion of the investigator. Subjects should be on a stable dose of steroids for at least 1 week prior to study beginning.)
• Chemotherapy administered within 4 weeks (6 weeks for an IV nitrosoureas and 12 weeks for an implanted nitrosoureas wafer) prior to Day 1 of study treatment.
• Pregnancy or breastfeeding.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection requiring IV antibiotics \& psychiatric illness/social situations that would limit adherence with study requirements, or disorders associated with significant immunocompromised state.
• Known previous/current malignancy requiring treatment within ≤ 3 years except for cervical carcinoma in situ, squamous or basal cell skin carcinoma and superficial bladder carcinoma.
• Any comorbid condition that confounds the ability to interpret data from the study as judged by the Investigator.

Where it is running

• University of California, Irvine — Orange, California, United States

Full record on ClinicalTrials.gov

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