Open label, single-center, two-part pharmacokinetic study: Part I: Relative bioavailability study to compare the pharmacokinetics of BP1.4979 after administration of single oral doses of BP1.4979 as sustained release formulation and actual immediate release formulation, under fasting and fed conditions, in healthy subjects. Part II: Pharmacokinetics of BP1.4979 after a 14-day dosing period with b.i.d. administration of BP1.4979 as sustained release formulation in healthy subjects.

2024-512355-20-00 Protocol BP1.4979 / P24-01 Human pharmacology (Phase I) - Other Ended

Start 1 Aug 2024 · End 23 Oct 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol BP1.4979 / P24-01

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 32
Countries 1
Sites 1

Binge eating disorder

Key facts

Sponsor
Bioprojet Pharma
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Psychiatry and Psychology [F] - Behavior and Behavior Mechanisms [F01]
Trial duration
1 Aug 2024 → 23 Oct 2024
Decision date (initial)
2024-06-26
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

Binge eating disorder

VersionLevelCodeTermSystem organ class
24.0 PT 10004716 Binge eating 100000004873

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

CountryMS statusPlanned subjectsSites
Belgium Ended 32 1
Rest of world 0

Investigational sites

Belgium

1 site · Ended
Advanced Technology Corporation
Clinical Pharmacology Unit, Avenue De L'hopital 1, Etage 2e Tour 2 Route 124, Liege

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
Belgium 2024-08-01 2024-10-23 2024-08-01 2024-10-17

Application history

2 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-05-23 Belgium Acceptable
2024-06-26
2024-06-26
2 NON SUBSTANTIAL MODIFICATION NSM-1 2024-10-24 Belgium Acceptable
2024-06-26
2024-10-24