Overview
Sponsor-declared trial summary
Phase
Human pharmacology (Phase I) - Other
Status
Ended
Participants planned
20
Countries
1
Sites
1
Anaphylaxis
Key facts
- Sponsor
- Bioprojet Pharma
- Participant type
- Healthy volunteers
- Age range
- 18-64 years
- Gender
- Male
- Therapeutic area
- Diseases [C] - Cardiovascular Diseases [C14]
- Trial duration
- 3 May 2024 → 4 Sep 2024
- Decision date (initial)
- 2024-03-25
- 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
Anaphylaxis
| Version | Level | Code | Term | System organ class |
|---|---|---|---|---|
| 20.0 | LLT | 10002218 | Anaphylaxis | 10021428 |
Sponsors and contacts
Sponsor organisations, regulatory contacts, third parties
Bioprojet Pharma
- Sponsor organisation
- Bioprojet Pharma
- Address
- 9 Rue Rameau
- City
- Paris
- Postcode
- 75002
- Country
- France
Scientific contact point
- Organisation
- Bioprojet Pharma
- Contact name
- Clinical Development Director
Public contact point
- Organisation
- Bioprojet Pharma
- Contact name
- Clinical Development Director
Locations
1 EU/EEA country · 1 investigational sites
By country
| Country | MS status | Planned subjects | Sites |
|---|---|---|---|
| France | Ended | 20 | 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 |
|---|---|---|---|---|---|
| France | 2024-05-03 | 2024-09-04 | 2024-05-03 | 2024-09-04 |
Application history
1 submissions — initial application plus substantial / non-substantial modifications
| # | Type | Code | Submitted | Reference MS | Conclusion | Decision date |
|---|---|---|---|---|---|---|
| 1 | INITIAL | IN | 2023-11-24 | France | Acceptable 2024-03-25
|
2024-03-25 |