Bioequivalence clinical trial of two formulations of ezetimibe/atorvastatin

2024-520303-62-00 Protocol N-EZEATO-24-293 Human pharmacology (Phase I) - Bioequivalence study Ended

Start 4 Mar 2025 · End 20 May 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol N-EZEATO-24-293

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ended
Participants planned 36
Countries 1
Sites 1

Healthy volunteers

Key facts

Sponsor
Laboratorios Normon S.A.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
4 Mar 2025 → 20 May 2025
Decision date (initial)
2025-02-18
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 volunteers

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Laboratorios Normon S.A.

Sponsor organisation
Laboratorios Normon S.A.
Address
Ronda De Valdecarrizo 6
City
Tres Cantos
Postcode
28760
Country
Spain

Scientific contact point

Organisation
Laboratorios Normon S.A.
Contact name
Carlos Govantes (R&D Director)

Public contact point

Organisation
Laboratorios Normon S.A.
Contact name
Carlos Govantes (R&D Director)

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Spain Ended 36 1
Rest of world 0

Investigational sites

Spain

1 site · Ended
Hospital Universitario De La Princesa
Clinical Pharmacology Department, Calle De Diego De Leon 62, 28006, Madrid

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Spain 2025-03-04 2025-05-20 2025-03-05 2025-03-21

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-02-06 Spain Acceptable
2025-02-17
2025-02-18