A Study to find out the safety, tolerability and interaction of drug with body (including the effect of Itraconazole on RO7268489) and also what the body does to RO7268489 after oral intake by healthy participants

2024-510606-85-00 Protocol BP45248 Human pharmacology (Phase I) - Other Ended

Start 10 May 2024 · End 14 Jun 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol BP45248

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 34
Countries 1
Sites 1

Not applicable

Key facts

Sponsor
F. Hoffmann-La Roche AG
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
10 May 2024 → 14 Jun 2025
Decision date (initial)
2024-05-03
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

Not applicable

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

F. Hoffmann-La Roche AG

Sponsor organisation
F. Hoffmann-La Roche AG
Address
Grenzacherstrasse 124
City
Basel
Postcode
4058
Country
Switzerland

Scientific contact point

Organisation
F. Hoffmann-La Roche AG
Contact name
Trial Information System - TISL

Public contact point

Organisation
F. Hoffmann-La Roche AG
Contact name
Trial Information System - TISL

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Ended 34 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Pharmaceutical Research Associates Group B.V.
Program Management, Van Swietenlaan 6, 9728 NZ, Groningen

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Netherlands 2024-05-10 2025-06-13 2024-05-10 2025-03-05

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-03-12 Netherlands Acceptable
2024-05-03
2024-05-03
2 SUBSTANTIAL MODIFICATION SM-1 2024-09-16 Netherlands Acceptable
2024-10-21
2024-10-21
3 NON SUBSTANTIAL MODIFICATION NSM-1 2025-03-19 Netherlands Acceptable
2024-10-21
2025-03-19
4 NON SUBSTANTIAL MODIFICATION NSM-2 2025-05-29 Netherlands Acceptable
2024-10-21
2025-05-29
5 SUBSTANTIAL MODIFICATION SM-2 2025-06-11 Netherlands Acceptable
2025-06-24
2025-06-24