Randomized, crossover, comparative bioavailability study of two Paracetamol-Ibuprofen 25-20 mg/ml oral suspension, administered in single dose to healthy subjects under fasting conditions.

2024-519661-22-00 Protocol FMLD-UMBRIA-62 Human pharmacology (Phase I) - Other Ended

Start 3 Mar 2025 · End 23 Apr 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol FMLD-UMBRIA-62

Overview

Sponsor-declared trial summary

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

Healthy volunteers

Key facts

Sponsor
Farmalider S.A.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
3 Mar 2025 → 23 Apr 2025
Decision date (initial)
2025-02-18
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Healthy volunteers

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Farmalider S.A.

Sponsor organisation
Farmalider S.A.
Address
Calle De La Granja 1 Planta 3
City
Alcobendas
Postcode
28108
Country
Spain

Scientific contact point

Organisation
Farmalider S.A.
Contact name
Carlos Calandria

Public contact point

Organisation
Farmalider S.A.
Contact name
Carlos Calandria

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Spain Ended 24 1
Rest of world 0

Investigational sites

Spain

1 site · Ended
Hospital Clinico San Carlos
Farmacologia Clinica, Calle Del Profesor Martín Lagos S/n, 28040, 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 2025-03-03 2025-04-23 2025-03-11 2025-03-27

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-01-23 Spain Acceptable
2025-02-18
2025-02-18