Vorasidenib Expanded Access Program

Trial Title: Vorasidenib Expanded Access Program

NCT ID: NCT05592743

Condition: Glioma
Recurrence
Disease Attributes
Pathologic Processes
Neoplasms, Neuroepithelial
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms, Nerve Tissue

Conditions: Official terms:
Neoplasms
Glioma
Neuroectodermal Tumors
Neuroectodermal Tumors, Primitive
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Neoplasms, Germ Cell and Embryonal
Neoplasms, Nerve Tissue
Neoplasms, Neuroepithelial
Recurrence
Pathologic Processes
Disease Attributes

Conditions: Keywords:
Vorasidenib
AG-881
S95032
Glioma
Oligodendroglioma
Astrocytoma
IDH-1
IDH-2

Study type: Expanded Access

Overall status: Approved for marketing

Intervention:

Intervention type: Drug
Intervention name: Vorasidenib
Description: Oral therapy

Other name: AG-881, S95032

Summary: This is an expanded access program to provide vorasidenib for treatment of patients 12 years or older with IDH1- or IDH2-mutated glioma.

Detailed description: This expanded access program is designed to provide access to vorasidenib for patients with IDH1- or IDH2-mutated glioma who are not eligible for other vorasidenib clinical trials, and who in the opinion of the treating oncologist would potentially benefit from treatment with vorasidenib. Safety assessments (including vital signs, hematology, and serum chemistry) occur every two weeks for the first two cycles (28 day each cycle), then monthly for the duration of treatment. Treatment with vorasidenib will continue until, in the clinical judgement of the treating physician, the patient is no longer benefiting from the treatment, vorasidenib is approved and available by prescription, or the study is terminated. Requests by treating physicians to file a single patient investigational new drug application as part of the expanded access program for vorasidenib will be considered on a case-by-case basis.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Male and females; ages ≥ 12 years old. 2. IDH-mutant oligodendroglioma or astrocytoma with the IDH1 or IDH2 gene mutation confirmed by tissue-based diagnosis. 3. At least 1 prior surgery for glioma (including biopsy). 4. Adequate bone marrow function as evidenced by: - Absolute neutrophil count ≥ 1.5 X 109/L - Hemoglobin ≥ 9 g/dL - Platelets ≥ 100 X 109/L 5. Adequate hepatic function as evidenced by: - Serum total bilirubin ≤ 1.5 X upper limit of normal (ULN) - Aspartate aminotransferase and alanine aminotransferase: at or below the ULN - Alkaline phosphatase ≤ 2.5 X ULN 6. Adequate renal function as evidenced by a creatinine clearance (CrCl) ≥ 40 mL/min Exclusion criteria: 7. Patient is eligible for a clinical trial with vorasidenib. 8. Patients who are enrolled in a Servier-sponsored clinical trial and have completed all requirements of the trial may be eligible if the patient continues to benefit from vorasidenib and does not meet criteria for discontinuation of treatment. 9. Pregnant or breastfeeding. 10. Patients who require or who cannot withhold strong inhibitors of CYP1A2 (ciprofloxacin and fluvoxamine). Consider alternative therapies that are not strong CYP1A2 inhibitors.

Gender: All

Minimum age: 12 Years

Maximum age: N/A

Lead sponsor:
Agency: Servier
Agency class: Industry

Collaborator:
Agency: Servier Pharmaceuticals, LLC
Agency class: Other

Source: Servier

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05592743