RecruitingPhase 1NCT07102394

Feasibility and Tolerability of IMLYGIC for the Treatment of Cutaneous Neurofibromas in Adults With NF1

Studying Neurofibromatosis type 1

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Key facts

Sponsor
Johns Hopkins University
Principal Investigator
Carlos Romo, MD
Johns Hopkins University
Intervention
Imlygic(drug)
Enrollment
10 enrolled
Eligibility
18 years · All sexes
Timeline
20262027

Study locations (1)

Collaborators

Neurofibromatosis Therapeutic Acceleration Program · Amgen

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07102394 on ClinicalTrials.gov

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