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NCT06416800 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Effect of Povorcitinib on Digoxin, Rosuvastatin, and Metformin Pharmacokinetics and the Effect of Probenecid on Povorcitinib Pharmacokinetics When Administered Orally to Healthy Adult Participants

A Phase 1 study, sponsored by Incyte Corporation.

Completed
Registry status
Phase 1
Development phase
71
Enrollment target

NCT06416800 is a Phase 1 study that has completed, run by Incyte Corporation. The registered enrollment target is 71 participants.

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The verdict

NCT06416800, a Phase 1 study, has completed, sponsored by Incyte Corporation.

COMPLETED
Registry status
Phase 1
Development phase
71 participants
Enrollment target

Study Summary

The purpose of this study is to Assess the Effect of Povorcitinib on Digoxin, Rosuvastatin, and Metformin Pharmacokinetics and the Effect of Probenecid on Povorcitinib Pharmacokinetics When Administered Orally to Healthy Adult Participants.

Interventions

  • DRUG Metformin
  • DRUG Probenecid
  • DRUG Povorcitinib
  • DRUG Rosuvastatin
  • DRUG Digoxin

Trial Details

FieldValue
Enrollment Target 71 participants
Start Date 2024-06-19
Est. Completion 2025-01-15
Phase Phase 1

Sponsor

Incyte Corporation

239 total trials

What the Registry Record Tells You About NCT06416800

The ClinicalTrials.gov registry entry for NCT06416800 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 71 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Incyte Corporation, which has 239 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Metformin is the first listed.

NCT06416800 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06416800 about?

NCT06416800 is a clinical study titled "A Study to Assess the Effect of Povorcitinib on Digoxin, Rosuvastatin, and Metformin Pharmacokinetics and the Effect of Probenecid on Povorcitinib Pharmacokinetics When Administered Orally to Healthy Adult Participants". The purpose of this study is to Assess the Effect of Povorcitinib on Digoxin, Rosuvastatin, and Metformin Pharmacokinetics and the Effect of Probenecid on Povorcitinib Pharmacokinetics When Administered Orally to Healthy Adult Participants.

What is the current status of trial NCT06416800?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 71 participants. The study started on 2024-06-19. Estimated completion is 2025-01-15.

What interventions are being tested in trial NCT06416800?

The interventions under investigation include: Metformin (DRUG), Probenecid (DRUG), Povorcitinib (DRUG), Rosuvastatin (DRUG), Digoxin (DRUG).

Who is sponsoring clinical trial NCT06416800?

This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.