Actively Recruiting
A Window of Opportunity Trial of Mirdametinib Plus Vorinostat for NF1 Associated, H3K27 Trimethylation Deficient Malignant Peripheral Nerve Sheath Tumor [MPNST]
Led by University of Minnesota · Updated on 2026-02-03
8
Participants Needed
1
Research Sites
58 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a single center Phase 0 "window of opportunity" trial for the treatment of newly diagnosed, PRC2 deficient, primary malignant peripheral nerve sheath tumors (MPNSTs) with a short course of the combination of mirdametinib and vorinostat prior to the most appropriate standard of care treatment for their specific tumor (typically localized radiation followed by surgical resection). Four to eight patients, 12 years of age or older and meeting the study's biomarker inclusion criteria, would be enrolled onto this trial. After voluntary written consent (assent with parent consent for minors) the patient undergoes MRI and PET imaging of the tumor and a needle biopsy to collect tumor is performed. Patients with histone H3K27 trimethylation deficient MPNST, as confirmed by immunohistochemistry, receive a single 28-day course of mirdametinib and vorinostat at standard oral dosing for each. At day 26, 27, or 28 the patient returns to clinic for a research visit repeating the baseline MRI and PET imaging and the needle biopsy for tumor tissue. This ends direct study participation. The patient goes on to the most appropriate standard of care treatment for their MPNST. Information about the subsequent standard of care treatment is collected for the purposes of this study.
CONDITIONS
Official Title
A Window of Opportunity Trial of Mirdametinib Plus Vorinostat for NF1 Associated, H3K27 Trimethylation Deficient Malignant Peripheral Nerve Sheath Tumor [MPNST]
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Known Neurofibromatosis type 1 (NF-1) syndrome based on current diagnostic criteria.
- Diagnosis of suspected MPNST by PET or MRI imaging
- Confirmation of histone H3 lysine 27 trimethylation-negative MPSNT by immunohistochemistry
- Twelve years of age or older
- Complete blood count (CBC), platelet, liver and kidney function within institutional normal limits performed within 14 days of 1 st dose of study drug.
- Must be able to swallow capsules.
- Females of childbearing potential must use highly effective contraception from enrollment through 6 months after last dose; males with partners of childbearing potential must use contraception from enrollment through 3 months after last dose.
- Provides voluntary written consent prior to study activities, with parental/guardian consent and assent for ages 12 to 17 at enrollment.
You will not qualify if you...
- Pregnant or breastfeeding; females must have a negative pregnancy test within 7 days prior to first dose.
- Significant cardiac disease
- Significant eye disease
- Radiation therapy or chemotherapy in the past year.
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55414
Actively Recruiting
Research Team
K
Kris Beatrez
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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