Surgical Window of Opportunity Study of Orally Administered BAY 2402234 in Recurrent Glioma

- Adults ≥ 18 years of age

- Histologically and/or genomically documented recurrent or progressive astrocytoma, IDH-mutant, grade 3 or 4 (diagnosis established by the presence of an IDH1 or IDH2 mutation along with grade 3 or 4 radiographic findings)

- Interval of at least 12 weeks from completion of adjuvant radiotherapy for gliomas to dosing, or surgical confirmation of recurrent disease

- Performance status measured via Karnofsky Performance Score of ≥ 60

- Confirmed measurable disease per response assessment in neuro-oncology criteria (RANO)

- Participants should have at least one 1.5cm x 1.5cm region of enhancing and non-enhancing tumor within the surgically accessible region

- Ability of neurosurgeon to resect tumor

- Laboratory values at the Screening Visit:

- All men, as well as women of child-bearing potential must agree to use dual contraceptive methods (hormonal or barrier method of birth control; abstinence) while on the study drug and for 3 months afterward. Men must also refrain from sperm donation for 4 months after treatment with BAY 2402234. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.

- A female of child-bearing potential is any woman (regardless of sexual orientation, marital status, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:

- Ability to understand and the willingness to sign a written informed consent.

- Patients under age 18 (due to fundamental difference between pediatric and adult gliomas)

- Treatment with an IDH inhibitor within 90 days of enrollment

- Treatment with temozolomide less than 23 days from study initiation, treatment with CCNU or BCNU less than 42 days from study initiation, or treatment with any cancer-directed systemic therapy less than 4 weeks or 5 half-lives from study initiation, whichever is shorter

- Any immunomodulatory drug or molecularly targeted, monoclonal antibody, within 14 days prior to initiation of study drug

- Use of any investigational agents within 28 days of baseline or 5 half-lives from study initiation, whichever is shorter

- Increasing corticosteroid requirement or a dose of >24mg per day of dexamethasone or an equivalent dose of other corticosteroids for longer than 48 hours within 7 days prior to study initiation

- Radiotherapy within 12 weeks prior to registration unless surgical confirmation of recurrent disease

- Presence of an acute or chronic toxicity of prior chemotherapy, with the exception of alopecia or lymphopenia, that has not resolved to ≤ Grade 1, as determined by National Cancer Institute CTCAE v5.0

- Major surgery within 28 days prior to initiation of study drug

- Active or clinically unstable bacterial, viral, or fungal infection requiring systemic therapy

- Known human immunodeficiency virus or acquired immunodeficiency syndrome-related illness

- Any of the following within 6 months prior to initiation of study drug: uncontrolled congestive heart failure (New York Heart Association Classification 3 or 4), angina, myocardial infarction, cerebrovascular accident, coronary or peripheral artery bypass graft surgery, transient ischemic attack

- Pulmonary embolism within 1 month prior to initiation of study drug

- Unstable cardiac dysrhythmias or persistent prolongation of the QTc interval to >450 msec for males or >470 msec for females

- Any contraindication to contrast-enhanced MRI examination

- Evidence of clinically significant intracranial hemorrhage

- Previous history of an additional emergency, except for non-squamous-cell carcinoma of skin or carcinoma-in-situ of the uterine cervix, unless the tumor was treated with curative intent more than 2 years prior to study entry

- Requires anti-seizure medications that are known to be strong inducers of CYP3A4/5 enzymes (carbamazepine, phenobarbital, phenytoin). Strong inhibitors and/or strong inducers of CYP3A4 should not be administered within 14 days or 5 half-lives (whichever is shorter) of the start of BAY 2402234 treatment, or during BAY 2402234 treatment, unless there is an emergent or life-threatening medical condition

- Pregnant or lactating female

- Any severe, acute, or chronic medical or psychiatric condition, or laboratory abnormality that may increase the risk associated with study participation or study drug administration, may interfere with the informed consent process and/or with compliance with the requirements of the study, or may interfere with the interpretation of study results and, in the Investigator's opinion, would make the subject inappropriate for entry into this study

- Difficulty swallowing or malabsorption syndrome; refractory nausea & vomiting, chronic gastrointestinal disease or previous significant bowel resection with clinically significant sequelae that would preclude adequate absorption of study drug