Patient Guide: Astroscape: A Study of Radiprodil on Safety, Tolerability, Pharmacokinetics, and Effect on Seizures and Behavioral Symptoms in Patients With TSC or FCD Type II

We'll Help You Connect with This Trial

Quri.ai is a free clinical trial matching service. We help patients like you connect directly with research sites conducting this study.

✓ Get matched to the right study location for you
✓ Connect directly with study coordinators at 20 participating sites
✓ Understand eligibility with our simplified screening tool
✓ Free service - we're here to help you access clinical research

Trial ID: NCTNCT06392009

Status: 🟢 Enrolling Now

Condition: Tuberous Sclerosis, Seizures, Malformations of Cortical Development, Focal Cortical Dysplasia, Sclerosis, Behavioral Symptoms

Phase: PHASE1, PHASE2

Find a Study Location Near You

This study is available at 20 research sites. We'll help you connect with the location that's right for you.

Participating sites include:

• South Brisbane,
• Antwerp,
• Leuven,
• And 17 more locations - let us help you find the closest one

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Astroscape: A Study of Radiprodil on Safety, Tolerability, Pharmacokinetics, and Effect on Seizures and Behavioral Symptoms in Patients With TSC or FCD Type II - Join Clinical Trial NCTNCT06392009

How to Join This Clinical Trial - NCTNCT06392009

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Tuberous Sclerosis, Seizures, Malformations of Cortical Development, Focal Cortical Dysplasia, Sclerosis, Behavioral Symptoms. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Tuberous Sclerosis, Seizures, Malformations of Cortical Development, Focal Cortical Dysplasia, Sclerosis, Behavioral Symptoms. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied: Tuberous Sclerosis, Seizures, Malformations of Cortical Development, Focal Cortical Dysplasia, Sclerosis, Behavioral Symptoms
Treatment Being Tested: Investigational treatment
Study Phase: PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status: Currently enrolling participants
Study Identifier: NCTNCT06392009 - ClinicalTrials.gov Identifier
Sponsored By: Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

Initial screening to determine eligibility
Regular study visits and health assessments
Receiving the study treatment or placebo
Medical monitoring and follow-up care
Contributing to medical research that may help others
Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

Close medical monitoring by healthcare professionals
Access to potential new treatments
Compensation for time and travel (varies by study)
No-cost study-related medical care
The opportunity to help advance medical knowledge

Roma, 00168 - Italy

Status: RECRUITING

And 10 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Tuberous Sclerosis, Seizures, Malformations of Cortical Development, Focal Cortical Dysplasia, Sclerosis, Behavioral Symptoms:

Review the eligibility criteria with your healthcare provider
Contact the study team for a pre-screening interview
Schedule an in-person screening visit if eligible
Review and sign the informed consent form
Begin participation in the clinical trial

Why Choose Quri.ai as Your Clinical Trial Matching Service

Quri.ai is a free clinical trial matching service that helps patients connect with research sites. We make it easier to:

Find clinical trials that match your condition
Get matched to the right study location near you
Connect directly with study coordinators
Understand if you qualify with simplified eligibility screening
Navigate the enrollment process with personalized support
Access new treatments through clinical research participation