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NCT05437094

Effect of Coadministration of Itraconazole on the Pharmacokinetics of CRD-740

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

Phase 1 trial testing CRD-740 in Clinical Pharmacology in 20 participants. Completed in 10 August 2022.

Timeline
27 June 2022
Primary endpoint
3 August 2022
10 August 2022

Quick facts

Lead sponsorCardurion Pharmaceuticals, Inc.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment20
Start date27 June 2022
Primary completion3 August 2022
Estimated completion10 August 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Cardurion Pharmaceuticals, Inc. — full company profile →

Who can join

Adults 18 to 55, any sex, with Clinical Pharmacology or Pharmacokinetics. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a Phase 1, single-site, open-label, fixed sequence crossover study to investigate the effect of coadministration of itraconazole on the pharmacokinetics of CRD-740 in healthy male and female subjects. Subjects will be admitted into the study site on Day -1 and will be confined to the study site until discharge on Day 16. Subjects will receive CRD-740 orally on Days 1 and 10. Itraconazole will be given once daily, orally, on Days 7 through 15.

Publications & conference data

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

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Other trials of CRD-740

Trials testing the same drug.

Other recruiting trials for Clinical Pharmacology

Currently open trials in the same condition.

Other Cardurion Pharmaceuticals, Inc. trials

Trials by the same sponsor.

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Data sources for this page

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