Comparative Bioavailability of Teriflunomide 14 mg Film-Coated Tablets: A Single-Dose, Open-Label, Randomized, Two-Sequence, Two-Treatment, Two-Period Crossover Study in Healthy Subjects Under Fasting Conditions.

2024-516401-23-00 Protocol BLCL-TER-PIL01 Human pharmacology (Phase I) - Bioequivalence study Ended

End 24 Sep 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol BLCL-TER-PIL01

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ended
Participants planned 22
Countries 1
Sites 1

No medical condition.

Key facts

Sponsor
Tecnimede-Sociedade Tecnico-Medicinal S.A.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male
Therapeutic area
Not possible to specify
Trial duration
completed 24 Sep 2025
Decision date (initial)
2024-09-04
Transition trial
Yes
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

External identifiers

EU CT number
2024-516401-23-00
EudraCT number
2021-005027-20

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

Tecnimede-Sociedade Tecnico-Medicinal S.A.

Sponsor organisation
Tecnimede-Sociedade Tecnico-Medicinal S.A.
Address
Rua Da Tapada Grande 2 Abrunheira
City
Sintra
Postcode
2710-228
Country
Portugal

Scientific contact point

Organisation
Tecnimede-Sociedade Tecnico-Medicinal S.A.
Contact name
Rita Neves

Public contact point

Organisation
Tecnimede-Sociedade Tecnico-Medicinal S.A.
Contact name
Rita Neves

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Portugal Ended 22 1
Rest of world 0

Investigational sites

Portugal

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

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-08-09 Portugal Acceptable with conditions
2024-09-03
2024-09-04