Overview
Sponsor-declared trial summary
Phase
Human pharmacology (Phase I) - Other
Status
Ended
Participants planned
24
Countries
1
Sites
1
Epilepsy
Key facts
- Sponsor
- Rapport Therapeutics Inc.
- Participant type
- Healthy volunteers
- Age range
- 18-64 years
- Gender
- Male and Female
- Therapeutic area
- Diseases [C] - Nervous System Diseases [C10]
- Trial duration
- 19 Jun 2024 → 16 Dec 2024
- Decision date (initial)
- 2024-05-27
- Transition trial
- No
- Low-intervention
- No
- Rare-disease indication
- No
- Vulnerable population
- No
Trial design
CTIS Part I — objectives, methods, condition coding
Conditions and MedDRA coding
Epilepsy
| Version | Level | Code | Term | System organ class |
|---|---|---|---|---|
| 21.0 | PT | 10015037 | Epilepsy | 100000004852 |
Sponsors and contacts
Sponsor organisations, regulatory contacts, third parties
Rapport Therapeutics Inc.
- Sponsor organisation
- Rapport Therapeutics Inc.
- Address
- 1325 Boylston Street Suite 401
- City
- Boston
- Postcode
- 02215-3900
- Country
- United States
Scientific contact point
- Organisation
- Rapport Therapeutics Inc.
- Contact name
- Swamy Yeleswaram
Public contact point
- Organisation
- Rapport Therapeutics Inc.
- Contact name
- Swamy Yeleswaram
Locations
1 EU/EEA country · 1 investigational sites
By country
| Country | MS status | Planned subjects | Sites |
|---|---|---|---|
| Belgium | Ended | 24 | 1 |
| Rest of world | — | 0 | — |
Investigational sites
Country notifications
Trial-start, recruitment-start, end and early-termination notifications submitted per Member State
| Country | Trial start | Trial end | Recruitment start | Recruitment end | Early termination |
|---|---|---|---|---|---|
| Belgium | 2024-06-19 | 2024-12-16 | 2024-06-19 |
Application history
1 submissions — initial application plus substantial / non-substantial modifications
| # | Type | Code | Submitted | Reference MS | Conclusion | Decision date |
|---|---|---|---|---|---|---|
| 1 | INITIAL | IN | 2024-04-12 | Belgium | Acceptable 2024-05-27
|
2024-05-27 |