A study in healthy people to test how well repeated doses of BI 3032950 are tolerated

2023-503332-40-00 Protocol 1486-0002 Human pharmacology (Phase I) - Other Ended

Start 5 Sep 2023 · End 19 Aug 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol 1486-0002

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 40
Countries 1
Sites 1

Healthy

Key facts

Sponsor
Boehringer Ingelheim International GmbH, Boehringer Ingelheim International GmbH
Participant type
Healthy volunteers
Age range
18-64 years, 65+ years
Gender
Male
Therapeutic area
Phenomena and Processes [G] - Physiological processes [G07]
Trial duration
5 Sep 2023 → 19 Aug 2024
Decision date (initial)
2023-08-01
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

External identifiers

EU CT number
2023-503332-40-00
WHO UTN
U1111-1289-1904

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Healthy

VersionLevelCodeTermSystem organ class
21.0 LLT 10053349 Pharmacokinetic study 10022891

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Boehringer Ingelheim International GmbH

Sponsor organisation
Boehringer Ingelheim International GmbH
Address
Binger Strasse 173
City
Ingelheim Am Rhein
Postcode
55216
Country
Germany

Scientific contact point

Organisation
Boehringer Ingelheim International GmbH
Contact name
CT Disclosure & Data Transparency

Public contact point

Organisation
Boehringer Ingelheim International GmbH
Contact name
CT Disclosure & Data Transparency

Boehringer Ingelheim International GmbH

Sponsor organisation
Boehringer Ingelheim International GmbH
Address
Binger Strasse 173
City
Ingelheim Am Rhein
Postcode
55216
Country
Germany

Scientific contact point

Organisation
Boehringer Ingelheim International GmbH
Contact name
CT Disclosure & Data Transparency

Public contact point

Organisation
Boehringer Ingelheim International GmbH
Contact name
CT Disclosure & Data Transparency

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Belgium Ended 40 1
Rest of world 0

Investigational sites

Belgium

1 site · Ended
SGS Belgium
Clinical Pharmacology Unit, Drie Eikenstraat 655, 2650, Edegem

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 2023-09-05 2024-08-19 2023-09-15 2024-04-08

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2023-06-19 Belgium Acceptable with conditions
2023-07-31
2023-08-01
2 SUBSTANTIAL MODIFICATION SM-1 2023-08-07 Belgium Acceptable
2023-08-18
2023-08-18
3 NON SUBSTANTIAL MODIFICATION NSM-1 2023-11-20 Belgium Acceptable
2023-08-18
2023-11-20
4 NON SUBSTANTIAL MODIFICATION NSM-2 2024-07-08 Belgium Acceptable
2023-08-18
2024-07-08