Bioequivalence of Vortioxetine 5 mg Film-Coated Tablets in Healthy Participants Under Fasting Conditions.

2023-509422-21-00 Protocol CFA-1034-2-23 Human pharmacology (Phase I) - Bioequivalence study Ended

Start 17 Jul 2024 · End 23 Aug 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol CFA-1034-2-23

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ended
Participants planned 24
Countries 1
Sites 1

No medical condition.

Key facts

Sponsor
Laboratorios Cinfa S.A.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
17 Jul 2024 → 23 Aug 2024
Decision date (initial)
2024-05-06
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

Laboratorios Cinfa S.A.

Sponsor organisation
Laboratorios Cinfa S.A.
Address
Travesia De Roncesvalles 1, Olloki Olloki
City
Esteribar
Postcode
31699
Country
Spain

Scientific contact point

Organisation
Laboratorios Cinfa S.A.
Contact name
Medical Department

Public contact point

Organisation
Laboratorios Cinfa S.A.
Contact name
Medical Department

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Portugal Ended 24 1
Rest of world 0

Investigational sites

Portugal

1 site · Ended
Blueclinical Investigacao E Desenvolvimento Em Saude Lda.
Medical Management, Hospital Da Prelada 0 Floor And 3 rd Floor, Rua Sarmento De Beires 153, 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 2024-07-17 2024-08-23 2024-07-17 2024-07-26

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-03-06 Portugal Acceptable
2024-05-02
2024-05-06