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NCT07173738

Pharmacokinetics, Safety and Tolerability of Concurrent Doses of BIA 5-1058 and Furosemide

Completed Phase 1 Last updated 15 September 2025
What this trial tests

Phase 1 trial testing BIA 5-1058 in Pulmonary Arterial Hypertension in 44 participants. Completed in 7 September 2018.

Timeline
11 June 2018
Primary endpoint
7 September 2018
7 September 2018

Quick facts

Lead sponsorBial - Portela C S.A.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment44
Start date11 June 2018
Primary completion7 September 2018
Estimated completion7 September 2018
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Bial - Portela C S.A. — full company profile →

Who can join

Adults 18 to 55, any sex, with Pulmonary Arterial Hypertension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is: * To assess the effect of BIA 5 1058 400 mg on furosemide pharmacokinetics (PK). * To assess the effect of furosemide 40 mg on the PK of BIA 5 1058.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of BIA 5-1058

Trials testing the same drug.

Other recruiting trials for Pulmonary Arterial Hypertension

Currently open trials in the same condition.

Other Bial - Portela C S.A. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07173738.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing