A study in healthy volunteers to find out how long aticaprant stays in and acts on the body when administered with or without rabeprazole.

2023-510467-35-00 Protocol 67953964MDD1011 Human pharmacology (Phase I) - Other Ended

Start 5 Jun 2024 · End 29 Jul 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol 67953964MDD1011

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 18
Countries 1
Sites 1

Healthy Adult Participants.

Key facts

Sponsor
Janssen Cilag International
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Psychiatry and Psychology [F] - Mental Disorders [F03]
Trial duration
5 Jun 2024 → 29 Jul 2024
Decision date (initial)
2024-05-06
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Healthy Adult Participants.

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Janssen Cilag International

Sponsor organisation
Janssen Cilag International
Address
Turnhoutseweg 30
City
Beerse
Postcode
2340
Country
Belgium

Scientific contact point

Organisation
Janssen Cilag International
Contact name
CTIS Point of Contact

Public contact point

Organisation
Janssen Cilag International
Contact name
CTIS Point of Contact

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Belgium Ended 18 1
Rest of world 0

Investigational sites

Belgium

1 site · Ended
Janssen Pharmaceutica
ClinPharm Unit Merksem, Lange Bremstraat 70, 2170, Antwerp

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 2024-06-05 2024-07-29 2024-06-05 2024-07-12

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-03-15 Belgium Acceptable
2024-04-03
2024-05-06