Study of Sutent®/Sunitinib (SU11248) in Subjects With NF-1 Plexiform Neurofibromas

PHASE2TerminatedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

October 31, 2015

Study Completion Date

February 14, 2018

Conditions
NeurofibromatosisNF1Plexiform Neurofibromas
Interventions
DRUG

Sutent®/Sunitinib

Upon enrollment, subjects will receive Sutent® orally. Adults (Age \>18) will receive 25mg. Children will receive 10mg/m2/day. All subjects will take the daily dose for 28 days followed by a 14 day rest period. If subjects tolerate the initial dose, adults will be increased to 37.5mg and children will be increased to 15mg/m2/day. Again, subjects will take that dose for 28 days followed by a rest period of 14 days. Adults who tolerate the increase will go up to the maximum dose of 50mg. The maximum dose for children is 15mg/m2/day.

Trial Locations (1)

46202

Riley Hospital for Children at IU Health, Indianapolis

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

United States Department of Defense

FED

collaborator

Pfizer

INDUSTRY

lead

Indiana University

OTHER