A Study to Investigate the Effect of RO7504109 on Immune Cells in Healthy Participants

2025-522181-71-00 Protocol BP45669 Human pharmacology (Phase I) - Other Ended

Start 17 Sep 2025 · End 27 Feb 2026 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol BP45669

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 44
Countries 1
Sites 1

Not Applicable (N/A)

Key facts

Sponsor
F. Hoffmann-La Roche AG
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Health Care [N] - Population Characteristics [N01]
Trial duration
17 Sep 2025 → 27 Feb 2026
Decision date (initial)
2025-09-16
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 (N/A)

VersionLevelCodeTermSystem organ class
26.0 LLT 10088820 Clinical trial healthy volunteer 100000004848

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 44 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Centre for Human Drug Research
Immunology, Zernikedreef 8, 2333 CL, Leiden

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 2025-09-17 2025-09-24 2026-02-24

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-08-04 Netherlands Acceptable
2025-09-16
2025-09-16
2 SUBSTANTIAL MODIFICATION SM-1 2025-11-28