Placebo Controlled Study to Assess the Efficacy and Safety of Rapamycin in Drug Resistant Epilepsy Associated With Tuberous Sclerosis Complex

Recruiting Phase 3 Interventional Study
Tuberous Sclerosis Complex
Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
3 Months – 50
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
200 (estimated)
Sponsor
Katarzyna Kotulska · Other
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About This Trial

The purpose of the RaRE-TS study is to determine safety, tolerability and efficacy of rapamycin versus placebo in a drug resistant epilepsy associated with tuberous sclerosis complex (TSC).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * male or female aged from 3 months up to 50 years at the day of randomization * patients/parents/caregivers are willing to and able to give informed consent form for the participation in the study * patients/parents/caregivers are willing to and able to comply with all study re…
Contacts

Katarzyna Kotulska-Jozwiak

+48 22 8157404

k.kotulska@ipczd.pl

CONTACT

Monika Szkop

+48 22 815 74 88

m.szkop@ipczd.pl

CONTACT