Evaluating Bioequivalence of a Fixed Dose Combination versus Individual Tablets of Bempedoic Acid, Ezetimibe, and Atorvastatin.

2024-519849-29-00 Protocol DSE-BMP-0001-CIS-MA Human pharmacology (Phase I) - Bioequivalence study Ended

Start 27 Oct 2025 · End 14 Jan 2026 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol DSE-BMP-0001-CIS-MA

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ended
Participants planned 58
Countries 1
Sites 1

No medical condition.

Key facts

Sponsor
Daiichi Sankyo Europe GmbH
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
27 Oct 2025 → 14 Jan 2026
Decision date (initial)
2025-08-12
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

No medical condition.

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Daiichi Sankyo Europe GmbH

Sponsor organisation
Daiichi Sankyo Europe GmbH
Address
Zielstattstrasse 48, Thalkirchen-Obersendling Thalkirchen-Obersendling
City
Munich
Postcode
81379
Country
Germany

Scientific contact point

Organisation
Daiichi Sankyo Europe GmbH
Contact name
Clinical Trial Office

Public contact point

Organisation
Daiichi Sankyo Europe GmbH
Contact name
Clinical Trial Office

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Portugal Ended 58 1
Rest of world 0

Investigational sites

Portugal

1 site · Ended
Blueclinical Investigacao E Desenvolvimento Em Saude Lda.
Medical Management, Rua De Sarmento De Beires 153 0 Floor 3rd Floor, 4250-449, Porto

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Portugal 2025-10-27 2026-01-14 2025-10-27 2025-11-25

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-06-30 Portugal Acceptable
2025-08-11
2025-08-12
2 NON SUBSTANTIAL MODIFICATION NSM-1 2025-12-03 Portugal Acceptable
2025-08-11
2025-12-03