A single-arm open-label phase 2 study evaluating the efficacy and safety of abemaciclib in patients with recurrent oligodendroglioma
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- STATUS
- Recruiting
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- participants needed
- 15
Summary
This is a single-center, phase II, single-arm, open label study evaluating the efficacy and safety of abemaciclib for patients with recurrent oligodendroglioma (molecularly defined per the WHO 2016 guidance, i.e., presence of IDH mutation and 1p19q codeletion). The study will enroll 10 subjects who are evaluable for the studys primary endpoint (subjects must be receive at least one dose of abemacicilb to be evaluable for the primary endpoint). The study will be stratified by number of lines of prior alkylating chemotherapy (one prior line versus two or more prior lines). Eligibility criteria are such that of the 10 total subjects enrolled, at least 2 must have had only one prior line of alkylating chemotherapy.
Details
| Condition | Oligodendroglioma, Adult |
|---|---|
| Age | 99years or below |
| Clinical Study Identifier | TBD |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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