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RecruitingNCT06188741NF114Updated May 29, 2026

Selumetinib for the Prevention of Plexiform Neurofibroma Growth in NF Type 1

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

Phase
Phase 2
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
1 Year to 8 Years
Sex
All
01

Study 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.

Read the detailed description

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

02

Conditions studied

  • Neurofibromatosis 1
  • Plexiform Neurofibroma
03

Who can participate

Ages eligible
1 Year to 8 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

PART 1:

Inclusion Criteria:

  1. Age: > 1 (>12 months) and ≤8 years of age at the time of study enrollment.
  2. Diagnosis: Participants with a diagnosis of NF1 based on the 2021 revised consensus criteria [52] and
  3. 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.
  4. Physical exam at your institution within 1 year prior to consent.
  5. Written informed consent must be obtained from the legal guardians of all participants \<18 years of age.

Exclusion Criteria:

  1. Presence of a known, symptomatic PN with or without previous MRI imaging.
  2. Patients who have had previous whole-body MRI (WBMRI) are excluded from the study. However, patients who have had regional MRI(s) for an indication other than a PN and did not have a PN identified on previous MRI may still be eligible for the study.
  3. Inability to undergo MRI and/or contraindication for MRI examinations following the MRI protocol.
  4. Prior treatment with selumetinib or another specific MEK1/2 inhibitor.
  5. Evidence of an optic pathway or other low-grade glioma, high grade glioma, malignant peripheral nerve sheath tumor, or other cancer/tumor requiring treatment with chemotherapy, biologic therapy or radiation therapy.
  6. Ongoing radiation therapy, chemotherapy, hormonal therapy directed at a tumor, immunotherapy, or biologic therapy.
  7. Clinical judgement by the investigator that the patient should not participate in the study.

PART 2:

Inclusion Criteria:

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

      1. Major ("named") blood vessel OR
      2. Major ("named") airway OR
      3. Hollow viscus OR
      4. Spinal cord and foramina OR
      5. Vital Organs (including heart, lungs, liver, spleen, etc.)
  3. Body Surface Area (BSA): BSA ≥ 0.55 m2 [pending availability of granule formulation].
  4. 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.
  5. Able to swallow whole capsules [Pending availability of granule formulation].
  6. Hematologic Function: Absolute neutrophil count ≥1200/µL, hemoglobin ≥9g/dL, and platelets ≥100,000/µL (without transfusions).
  7. 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.
  8. 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

  9. Cardiac Function:

    1. 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).
    2. EKG with QTC or QTcF ≤450 msec.
  10. 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.

  11. Willingness to avoid excessive sun exposure and use adequate sunscreen protection if sun exposure is anticipated.
  12. 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.

Exclusion Criteria:

  1. Evidence of an optic pathway or other low-grade glioma, high-grade glioma, malignant peripheral nerve sheath tumor, or other cancer/tumor requiring treatment with chemotherapy, biologic therapy or radiation therapy.
  2. Ongoing radiation therapy, chemotherapy, hormonal therapy, immunotherapy, or biologic therapy directed at a tumor.
  3. Prosthesis, orthopedic implant, or dental braces that would interfere with volumetric analysis of target PN on MRI.
  4. Use of an investigational agent within the past 30 days.
  5. Any evidence of severe or uncontrolled systemic disease, active infection, active bleeding diatheses, or renal transplant, including any patient known to have hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) will be excluded.
  6. Participants who, in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study.
  7. Refractory nausea and vomiting, chronic gastrointestinal diseases (e.g., inflammatory bowel disease), or significant bowel resection that would preclude adequate absorption.
  8. Supplementation with vitamin E greater than 100% of the daily recommended dose. Any multivitamin containing vitamin E must be stopped prior to initiation of therapy.
  9. Participants not achieving adequate blood pressure despite antihypertensive therapy for control of blood pressure.
  10. Cardiac conditions:

    1. Known inherited coronary disease
    2. Symptomatic heart failure (NYHA Class II-IV prior or current cardiomyopathy, or severe valvular heart disease)
    3. Prior or current cardiomyopathy
    4. Severe valvular heart disease
    5. History of atrial fibrillation
  11. Ophthalmologic conditions:

    1. Current or past history of central serous retinopathy or retinal pigment epithelial detachment (RPED).
    2. Current or past history of retinal vein occlusion.
    3. History of radiation therapy that included the orbit in the field of treatment.
    4. Known intraocular pressure (IOP) > 21 mmHg (or ULN adjusted by age) or uncontrolled glaucoma (irrespective of IOP). Participants with known glaucoma and increased IOP who do not have meaningful vision (light perception only or no light perception) and are not experiencing pain related to the glaucoma, may be eligible after discussion with the Study Chair.
    5. Participants with any other significant abnormality on ophthalmic examination should be discussed with the Study Chair for potential eligibility.
    6. Ophthalmological findings secondary to long-standing optic pathway glioma (such as visual loss, optic nerve pallor or strabismus) will NOT be considered a significant abnormality for the purposes of the study.
  12. Known severe hypersensitivity to selumetinib or any excipient of selumetinib or history of allergic reactions attributed to compounds of similar chemical or biologic composition to selumetinib.
  13. Recent major surgery within a minimum of 4 weeks prior to starting study treatment.
  14. Any unresolved chronic toxicity with CTCAE grade ≥ 2 from previous therapy, except for alopecia.
  15. Receiving herbal supplements or medications known to be strong or moderate inhibitors or inducers of the cytochrome P450 (CYP)2C19 and CYP3A4 enzymes or fluconazole unless such products can be safely discontinued at least 14 days or 5 half-lives (whichever is longer) before the first dose of study medication.

PART 3:

Inclusion Criteria:

  1. 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).
  2. Body Surface Area (BSA): BSA ≥ 0.55 m2 [pending availability of granule formulation].
  3. 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.
  4. Able to swallow whole capsules [Pending availability of granule formulation].
  5. Hematologic Function: Absolute neutrophil count ≥1200/µL, hemoglobin ≥9g/dL, and platelets ≥100,000/µL (without transfusions).
  6. 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.
  7. 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

  8. Cardiac Function:

    1. 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).
    2. EKG with QTC or QTcF ≤450 msec.
  9. 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.

  10. Willingness to avoid excessive sun exposure and use adequate sunscreen protection if sun exposure is anticipated.
  11. 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.

Exclusion Criteria:

  1. Evidence of an optic pathway or other low-grade glioma, high-grade glioma, malignant peripheral nerve sheath tumor, or other cancer/tumor requiring treatment with chemotherapy, biologic therapy or radiation therapy.
  2. Ongoing radiation therapy, chemotherapy, hormonal therapy, immunotherapy, or biologic therapy directed at a tumor.
  3. Prosthesis, orthopedic implant, or dental braces that would interfere with volumetric analysis of target PN on MRI.
  4. Any evidence of severe or uncontrolled systemic disease, active infection, active bleeding diatheses, or renal transplant, including any patient known to have hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) will be excluded.
  5. Participants who, in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study.
  6. Refractory nausea and vomiting, chronic gastrointestinal diseases (e.g., inflammatory bowel disease), or significant bowel resection that would preclude adequate absorption.
  7. Supplementation with vitamin E greater than 100% of the daily recommended dose. Any multivitamin containing vitamin E must be stopped prior to initiation of therapy.
  8. Participants not achieving adequate blood pressure despite antihypertensive therapy for control of blood pressure.
  9. Cardiac conditions:

    1. Known inherited coronary disease
    2. Symptomatic heart failure (NYHA Class II-IV prior or current cardiomyopathy, or severe valvular heart disease)
    3. Prior or current cardiomyopathy
    4. Severe valvular heart disease
    5. History of atrial fibrillation
  10. Ophthalmologic conditions:

    1. Current or past history of central serous retinopathy or retinal pigment epithelial detachment (RPED).
    2. Current or past history of retinal vein occlusion.
    3. History of radiation therapy that included the orbit in the field of treatment.
    4. Known intraocular pressure (IOP) > 21 mmHg (or ULN adjusted by age) or uncontrolled glaucoma (irrespective of IOP). Participants with known glaucoma and increased IOP who do not have meaningful vision (light perception only or no light perception) and are not experiencing pain related to the glaucoma, may be eligible after discussion with the study chair.
    5. Participants with any other significant abnormality on ophthalmic examination should be discussed with the Study Chair for potential eligibility.
    6. Ophthalmological findings secondary to long-standing optic pathway glioma (such as visual loss, optic nerve pallor or strabismus) will NOT be considered a significant abnormality for the purposes of the study.
  11. Known severe hypersensitivity to selumetinib or any excipient of selumetinib or history of allergic reactions attributed to compounds of similar chemical or biologic composition to selumetinib.
  12. Recent major surgery within a minimum of 4 weeks prior to starting study treatment.
  13. Any unresolved chronic toxicity with CTC AE grade ≥ 2 from previous therapy, except for alopecia.
  14. Receiving herbal supplements or medications known to be strong or moderate inhibitors or inducers of the cytochrome P450 (CYP)2C19 and CYP3A4 enzymes or fluconazole unless such products can be safely discontinued at least 14 days or 5 half-lives (whichever is longer) before the first dose of study medication.
04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • 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

    Drug: Selumetinib

  • 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

    Drug: Selumetinib

Interventions

  • DrugSelumetinib

    Selumetinib (KoselugoTM) at the FDA approved dose of 25 mg/m2/dose PO BID

    Also known as: Koselugo

05

What researchers measure

Primary outcomes

  1. 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

Secondary outcomes

  1. 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

  2. PFS

    2\) PFS through one year after transitioning from continuous to an intermittent dosing schedule

    Time frame: 60 months

06

Study locations

15 of 15 sites recruiting
  • Childrens of Alabama
    Birmingham, Alabama 35233, United States
    Recruiting
  • Children's Hospital of Los Angeles
    Los Angeles, California 90027, United States
    • Tena Rosser, MD · Contact · trosser@chla.usc.org · 323-361-2471
    • Martha Arellano-Garcia, MS · Contact · margarcia@chla.usc.edu · 323-361-5812
    • Tena Rosser, MD · Principal investigator
    • Nathan Robison, MD · Sub investigator
    Recruiting
  • Stanford University
    Palo Alto, California 94304, United States
    • Cynthia Campen, MD · Contact · ccampen@stanford.edu · 650-497-8953
    • Cynthia Campen, MD · Principal investigator
    Recruiting
  • Children's National Hospital
    Washington D.C., District of Columbia 20010, United States
    Recruiting
  • Lurie Children's Hospital of Chicago
    Chicago, Illinois 60611, United States
    Recruiting
  • University of Chicago
    Chicago, Illinois 63637, United States
    Recruiting
  • Riley Hospital for Children/Indiana University
    Indianapolis, Indiana 46202, United States
    • Steven Rhodes, MD, PhD · Contact · RileyNFnurse@iuhealth.org · (317) 948-6641
    • Steven Rhodes, MD, PhD · Principal investigator
    Recruiting
  • Johns Hopkins University
    Baltimore, Maryland 21231, United States
    • Joshua Roberts, PhD · Contact · jrobe112@jhmi.edu · (410) 955-6827
    • Jaishri Blakeley, MD · Principal investigator
    Recruiting
  • National Cancer Institute/ National Institutes of Health
    Bethesda, Maryland 20892, United States
    • Hemaxi Patel · Contact · hemaxi.patel@nih.gov · 240-243-8838
    • Brigitte Widemann, MD · Principal investigator
    Recruiting
  • Boston Children's Hospital
    Boston, Massachusetts 02115, United States
    Recruiting
  • Mayo Clinic
    Rochester, Minnesota 55905, United States
    Recruiting
  • Washington University - St. Louis
    St Louis, Missouri 63110, United States
    • Amy Armstrong, MD · Contact · armstrongae@wustl.edu · 314-454-6018
    • Amy Armstrong, MD · Principal investigator
    Recruiting
  • Cincinnati Childrens Hospital Medical Center
    Cincinnati, Ohio 45229-, United States
    Recruiting
  • Children's Hospital of Philadelphia
    Philadelphia, Pennsylvania 19104, United States
    • Ratnakar Patti · Contact · pattir@email.chop.edu · 267-426-5503
    • Michael Fisher, MD · Principal investigator
    Recruiting
  • University of Texas, Southwestern
    Dallas, Texas 75390, United States
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06188741
Lead sponsor
University of Alabama at Birmingham
Collaborators
Children's Hospital of Philadelphia, Congressionally Directed Medical Research Programs
Responsible party
Girish Dhall, MD (Chair of NFCTC, University of Alabama at Birmingham) — Principal investigator
First posted
Jan 3, 2024
Start date
Aug 27, 2025
Primary completion
Sep 1, 2031 (estimated)
Completion
Sep 1, 2032 (estimated)
Last update
May 29, 2026

Study contacts

Karen Cole-Plourde, BA
Contact
kplourde@uab.edu
2055141317
Juliette Southworth, BS
Contact
jsouthworth@uab.edu
2055298967

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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