Phase 2 Trial of Selumetinib for the Prevention of Plexiform Neurofibroma Growth and Morbidity in Neurofibromatosis Type 1

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Plexiform neurofibromas (PN) are known to cause significant morbidity in children with NF1. The recent FDA approval for selumetinib in children 2 years and older with inoperable symptomatic PN was based on the finding that selumetinib shrinks the majority of PN in children with NF1 and results in clinically meaningful benefit such as improvement in pain or range of motion. However, many morbidities, such as blindness or nerve damage, cannot be fully reversed with PN shrinkage. Therefore, there remains a critical need in this patient population to determine if young participants with PN in high-risk locations may benefit from early medical intervention prior to the development of clinical problems. This study will determine whether participants with asymptomatic PN in high-risk locations can potentially benefit from early treatment with selumetinib.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Maximum Age: 8
Healthy Volunteers: f
View:

• Age: \> 1 (\>12 months) and ≤8 years of age at the time of study enrollment.

• Diagnosis: Participants with a diagnosis of NF1 based on the 2021 revised consensus criteria \[52\] and

• No known PN (prior to enrollment on Part 1). Participants for whom there is clinical suspicion for a PN (e.g., subtle facial asymmetry or large overlying hyperpigmented area) may be included in the study after discussion with the Study Chair so long as they have not previously had an MRI of the region of concern and are otherwise asymptomatic.

• Physical exam at your institution within 1 year prior to consent.

• Written informed consent must be obtained from the legal guardians of all participants \<18 years of age.

• Enrolled on Part 1 of this study and completed baseline WBMRI within 6 weeks of planned enrollment on Part 2.

• A measurable (≥3 mL) PN in a high-risk location as defined below (this must be confirmed by Study Chair or a member of the Study Committee prior to enrollment on Part 2).

‣ In the head or neck (with the exception of isolated scalp lesions) OR

⁃ Within the brachial or lumbosacral plexus OR

⁃ Adjacent to high-risk structure(s), defined as:

⁃ Major (named) blood vessel OR

• Major (named) airway OR

• Hollow viscus OR

• Spinal cord and foramina OR

• Vital Organs (including heart, lungs, liver, spleen, etc.)

• Body Surface Area (BSA): BSA ≥ 0.55 m2 \[pending availability of granule formulation\].

• Performance status: Lansky performance ≥70%. Participants who are wheelchair bound because of paralysis or immobility secondary to a non-PN related manifestation of NF1 (such as tibial pseudarthrosis or severe scoliosis) should be considered ambulatory when they are in their wheelchair.

• Able to swallow whole capsules \[Pending availability of granule formulation\].

• Hematologic Function: Absolute neutrophil count ≥1200/µL, hemoglobin ≥9g/dL, and platelets ≥100,000/µL (without transfusions).

• Hepatic Function: Bilirubin within 1.5 x the upper limit of normal for age, with the exception of those with Gilbert syndrome, and AST/ALT within ≤ 3 x upper limit of normal.

• Renal Function: Creatinine clearance or radioisotope GFR ≥60ml/min/1.73 m2 or a normal serum creatinine based on age, described in the table below.

• Age (years) Maximum Serum Creatinine (mg/dL)

• ≤5 0.8 \>5 to ≤10 1.0 \>10 to ≤15 1.2 \>15 1.5

• Cardiac Function:

∙ Normal ejection fraction (ECHO or cardiac MRI) ≥ 53% (or the institutional normal; if a range is given then the upper value of the range will be used).

‣ EKG with QTC or QTcF ≤450 msec.

⁃ Adequate Blood Pressure defined as:

⁃ A blood pressure (BP) ≤ the 95th percentile for age, height, and gender. Adequate blood pressure can be achieved using medication for treatment of hypertension. Participants must be on stable antihypertensive regimen for at least 30 days prior to study entry.

⁃ Willingness to avoid excessive sun exposure and use adequate sunscreen protection if sun exposure is anticipated.

⁃ Willingness to avoid the ingestion of grapefruit and Seville oranges (as well as other products containing these fruits, e.g., grapefruit juice or marmalade) during the study, as these may affect selumetinib metabolism.

• Enrolled on Part 2 of this study and had PN growth \>20% OR development of PN related symptom(s) while on observation portion of Part 2 (including the first 2 years for the observation arm OR during first year of observation after treatment with selumetinib).

• Body Surface Area (BSA): BSA ≥ 0.55 m2 \[pending availability of granule formulation\].

• Performance status: Lansky performance ≥70%. Participants who are wheelchair bound because of paralysis or immobility secondary to a non-PN related manifestation of NF1 (such as tibial pseudarthrosis or severe scoliosis) should be considered ambulatory when they are in their wheelchair.

• Able to swallow whole capsules \[Pending availability of granule formulation\].

• Hematologic Function: Absolute neutrophil count ≥1200/µL, hemoglobin ≥9g/dL, and platelets ≥100,000/µL (without transfusions).

• Hepatic Function: Bilirubin within 1.5 x the upper limit of normal for age, with the exception of those with Gilbert syndrome, and AST/ALT within ≤ 3 x upper limit of normal.

• Renal Function: Creatinine clearance or radioisotope GFR ≥60mL/min/1.73 m2 or a normal serum creatinine based on age, described in the table below.

• Age (years) Maximum Serum Creatinine (mg/dL)

• ≤5 0.8 \>5 to ≤10 1.0 \>10 to ≤15 1.2 \>15 1.5

• Cardiac Function:

∙ Normal ejection fraction (ECHO or cardiac MRI) ≥ 53% (or the institutional normal; if a range is given then the upper value of the range will be used).

‣ EKG with QTC or QTcF ≤450 msec.

• Adequate Blood Pressure defined as:

• A blood pressure (BP) ≤ the 95th percentile for age, height, and gender. Adequate blood pressure can be achieved using medication for treatment of hypertension. Participants must be on stable antihypertensive regimen for at least 30 days prior to study entry.

⁃ Willingness to avoid excessive sun exposure and use adequate sunscreen protection if sun exposure is anticipated.

⁃ Willingness to avoid the ingestion of grapefruit and Seville oranges (as well as other products containing these fruits, e.g., grapefruit juice or marmalade) during the study, as these may affect selumetinib metabolism.

Locations
United States
Alabama
Childrens of Alabama
RECRUITING
Birmingham
Ohio
Cincinnati Childrens Hospital Medical Center
RECRUITING
Cincinnati
Pennsylvania
Children's Hospital of Philadelphia
RECRUITING
Philadelphia
Contact Information
Primary
Karen Cole-Plourde, BA
kplourde@uab.edu
2055141317
Backup
Juliette Southworth, BS
jsouthworth@uab.edu
2055298967
Time Frame
Start Date: 2025-08-27
Estimated Completion Date: 2032-09-01
Participants
Target number of participants: 200
Treatments
No_intervention: Part 1: WBMRI for NF1 patients with no known PN
To assess the incidence of asymptomatic PN in any location in participants with NF1 and no known PN
Experimental: Part 2: Treatment randomization to selumetinib vs observation
To determine if selumetinib treatment prevents PN growth in young participants with asymptomatic tumors in high-risk locations
Experimental: Part 3: Part 2 participants with growing or symptomatic PN
To assess the proportion of participants who are able to maintain tumor response after transition to an intermittent dosing schedule
Sponsors
Collaborators: Congressionally Directed Medical Research Programs, Children's Hospital of Philadelphia
Leads: University of Alabama at Birmingham

This content was sourced from clinicaltrials.gov