Study of AG-120 and AG-881 in Subjects With Low Grade Glioma
Completed · Phase 1
Conditions studied: Glioma
In brief
Study to evaluate the suppression of 2-HG (2-hydroxyglutarate) in IDH-1 mutant gliomas in resected tumor tissue following pre-surgical treatment with AG-120 or AG-881.
Key facts
- Study ID
- NCT03343197
- Run by
- Institut de Recherches Internationales Servier
- People needed
- 49
- Starts
- 2018-03-20
- Expected to finish
- 2025-03-28
- Last updated by the study team
- 2026-02-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Be ≥18 years of age.
- Have histologically or cytologically confirmed recurrent Grade 2 or 3 LGG (oligodendroglioma or astrocytoma according to World Health Organization 2016 classification).
- Have documented IDH1 R132H gene mutation by local testing and known 1p19q or ATRX mutation status by local testing.
- Have central confirmation of primarily non-enhancing disease by MRI with less than or equal to 5 mm slice thickness and up to 1 mm interslice gap on either 2D T2 weighted image, 3D T2 weighted image, or FLAIR, with at least 1 non-enhancing tumor measuring 1×1×1 cm.
- Be candidates for clinical resection but for whom surgery is not urgently indicated (eg, for whom surgery within the next 2-4 months is appropriate).
- Have KPS of ≥60%
- Have expected survival of ≥12 months.
You may not qualify if…
- Have received prior systemic anti-cancer therapy within 1 month of the first dose of AG-120 or AG-881 or have received an investigational agent <14 days prior to their first dose of AG-120 or AG-881. In addition, the first dose of AG-120 or AG-881 should not occur before a period of ≥5 half-lives of the investigational agent has elapsed.
- Have had radiation within 6 months of the first dose of AG-120 or AG-881. (Note: Prior biopsy or surgery is allowed.)
- Have received any prior treatment with an IDH inhibitor.
- Have received any prior treatment with bevacizumab (Avastin).
Where it is running
- United States, California — Los Angeles, California, United States
- United States, California — San Francisco, California, United States
- United States, Massachusetts — Boston, Massachusetts, United States
- United States, New York — New York, New York, United States
- United States, North Carolina — Durham, North Carolina, United States
- United States, Texas — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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