Trials / Recruiting
RecruitingNCT05879146
Evaluation of the Response and Non-response of Nirogacestat in Desmoid Tumors- Clinical Study
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- Sponsor
- M.D. Anderson Cancer Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To learn about the safety and effects of an investigational drug called nirogacestat when given to participants with a desmoid tumor/aggressive fibromatosis
Detailed description
Primary Objectives: • To identify biomarkers associated with response and non-response to nirogacestat in participants with desmoid tumors (DT). Secondary Objectives: * To assess the 12-month progression-free survival (PFS of participants with DT who receive nirogacestat at 150 mg or 100 mg BID. * To assess MRI volumetric and functional parameters associated with response and non-response to nirogacestat in participants with DT. * To evaluate the histopathological changes in DT biopsy specimens. * To evaluate the safety and tolerability of nirogacestat in participants with DT. Exploratory Objectives: * To assess clinical benefit and tumor response by additional MRI-based measurements including MRI-modified Choi criteria and WHO. * To evaluate MRI parameters such as intensity histogram analysis from T2-weighted image (T2-WI), short inversion time inversion-recovery (T2-STIR), diffusion-weighted imaging (DWI) with apparent diffusion coefficient (ADC) mapping, post-contrast Water Dixon, perfusion-weighted imaging, and susceptibility-weighted imaging (SWI) with contrast and correlate with therapeutic response and clinical outcome. * To assess the dynamics and concordance of circulating tumor cells (CTCs) in the blood compartment and tumor burden during nirogacestat treatment. * To identify cell-free DNA (cfDNA) biomarkers associated with response and non-response to nirogacestat in patients with DT. * To understand the impact of dose on the incidence of ovarian dysfunction in women of childbearing potential (WOCBP).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nirogacestat | Given by PO |
Timeline
- Start date
- 2024-11-26
- Primary completion
- 2027-01-31
- Completion
- 2028-01-31
- First posted
- 2023-05-30
- Last updated
- 2026-04-13
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05879146. Inclusion in this directory is not an endorsement.