RENAISSANCE Study: A Phase 2, Multicenter, Open Label Safety and Tolerability Study of SPN-817 in Adult Patients With Treatment Resistant Epilepsy
Supernus Pharmaceuticals, Inc.
Summary
This study will evaluate the safety and tolerability of SPN-817 in adults with treatment resistant seizures
Description
This is a multicenter, three-phase, long-term open-label study assessing the safety and tolerability of SPN-817 (huperzine A, an acetylcholinesterase inhibitor) in adults 18-70 years of age with treatment resistant epilepsy. The Screening period is up to 8 weeks in duration, followed by a Titration Period of 9 weeks and a Maintenance Period of 12 weeks (total Treatment Period of 21 weeks) for eligible participants. The Treatment Period will be followed by an optional Open-Label Extension period which is up to 52 weeks in duration. Schedule A will enroll participants with treatment resistant se…
Eligibility
- Age range
- 18–70 years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: 1. A diagnosis of treatment resistant epilepsy as adjudicated by the Epilepsy Study Consortium. 2. Is male or female, aged 18 to ≤ 70 years at screening. 3. Is able to read, understand, and sign the Informed Consent Form (ICF). If the participant is unable to sign informed consent, a Legally Authorized Representative (LAR) will complete the ICF. 4. Ability to keep accurate seizure diaries (with the aid of a caregiver as needed). 5. Weight within the normal or overweight ranges according to accepted values of the Body Mass Index Chart (18.0 to 40 kg/m2). 6. Is able to swall…
Interventions
- DrugSPN-817
oral capsule
Locations (10)
- Green Leaf Clinical Trials, LLCJacksonville, Florida
- Visionary Investigators NetworkMiami, Florida
- Prince of Wales HospitalRandwick, New South Wales
- Royal Prince Alfred HospitalSydney, New South Wales
- Westmead HospitalSydney, New South Wales
- Royal Brisbane and Women's HospitalBrisbane, Queensland