Rapamycin
Drugoral administration
NCT Number: NCT03243019
To evaluate the efficacy of Rapamycin in extended cervicofacial lymphatic malformations in pediatric patients. Rapamycin is administered oral for a 6 month period.
The success rate is determined by volume reduction superior to 1/5e of the initial volume measured by MRI, impact on QOL and reduction of bleeding in case of mucosal involvement.
Interested in participating?
Request InfoUp to 18 year
All sexes
Interventional
Phase 2
Hôpital Jeanne de Flandres, CHU, Lille, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
oral administration
cervicofacial MRI
Biological dosage of Rapamycin level
Time frame: At 3 months
Volumetric assessment by MRI. A response is considered as positive if volume decrease is superior to 1/5th of the initial volume.
Time frame: At 3, 6 and 12 months
MRI assessment of the volume
Time frame: At 3, 6 and 12 months
Clinical and fiberscopy evaluation by scoring
Time frame: Baseline, at 3, 6 and 12 months
Assesses health-related quality of life among children with chronic and acute diseases
Time frame: Baseline and at 6 months
biological effect of mTOR blockage by measuring pAKT, p70S6 kinase, pMEK, and VEGF C, VEGFR3
Time frame: Monthly during 1 years
Side effect assessment using the NCI-CTC 3.0 scale
Contact information is provided by the study sponsor or research team.
University Hospital, Lille
Other
Evaluation of the Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations of Poor Prognosis
Acronym: RAPAMALYMPH
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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