A Phase 2 interventional study of Selumetinib in Neurofibromatosis 1 and Plexiform Neurofibroma, sponsored by University of Alabama at Birmingham. Recruiting at 15 sites in United States. Open to participants aged 1 Year to 8 Years. Per ClinicalTrials.gov, last updated 2026-05-29.
Sponsored by University of Alabama at Birmingham · Phase 2, Interventional, and Treatment
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.
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.
Other: This trial will be operated through the Neurofibromatosis Clinical Trials Consortium, funded by the Congressionally Directed Medical Research Program under the Department of Defense which consists of 24 sites throughout the United States.
Intervention: Selumetinib (KoselugoTM) at the FDA approved dose of 25 mg/m2/dose PO BID.
Study Duration: 7 years Partcipant Durations: 5 years
PART 1:
Inclusion Criteria:
Exclusion Criteria:
PART 2:
Inclusion Criteria:
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).
Adjacent to high-risk structure(s), defined as:
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:
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.
Exclusion Criteria:
Cardiac conditions:
Ophthalmologic conditions:
PART 3:
Inclusion Criteria:
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:
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.
Exclusion Criteria:
Cardiac conditions:
Ophthalmologic conditions:
To assess the incidence of asymptomatic PN in any location in participants with NF1 and no known PN
To determine if selumetinib treatment prevents PN growth in young participants with asymptomatic tumors in high-risk locations
Drug: Selumetinib
To assess the proportion of participants who are able to maintain tumor response after transition to an intermittent dosing schedule
Drug: Selumetinib
Selumetinib (KoselugoTM) at the FDA approved dose of 25 mg/m2/dose PO BID
Also known as: Koselugo
Progression free survival (PFS)
Progression free survival (PFS) in the group treated with selumetinib compared to those in the observation group
Time frame: 60 months
Participants found to have a previously unknown measurable PN
Proportion of participants found to have a previously unknown measurable PN in any location on WBMRI imaging
Time frame: 60 months
PFS
2\) PFS through one year after transitioning from continuous to an intermittent dosing schedule
Time frame: 60 months
Plan to share: No
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University of Alabama at Birmingham