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A Study to Assess the Effect of Povorcitinib on Digoxin, Rosuvastatin, and Metformin Pharmacokinetics When Administered Orally to Healthy Adult Participants - Trial NCT06416800

Access comprehensive clinical trial information for NCT06416800 through Pure Global AI's free database. This Phase 1 trial is sponsored by Incyte Corporation and is currently Not yet recruiting. The study focuses on Healthy Participants. Target enrollment is 54 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06416800
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06416800
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A Study to Assess the Effect of Povorcitinib on Digoxin, Rosuvastatin, and Metformin Pharmacokinetics When Administered Orally to Healthy Adult Participants
An Open-Label Study to Assess the Effect of Povorcitinib on Digoxin, Rosuvastatin, and Metformin Pharmacokinetics When Administered Orally to Healthy Adult Participants

Study Focus

Healthy Participants

Digoxin

Interventional

drug

Sponsor & Location

Incyte Corporation

Dallas, United States of America

Timeline & Enrollment

Phase 1

Jun 19, 2024

Aug 10, 2024

54 participants

Primary Outcome

Pharmacokinetic (PK) in plasma digoxin,PK in plasma rosuvastatin,PK in plasma metformin

Summary

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

ICD-10 Classifications

Seeking and accepting physical, nutritional and chemical interventions known to be hazardous and harmful
Healthy person accompanying sick person
Routine general health check-up of sports teams
Obesity
Persons with potential health hazards related to communicable diseases

Data Source

ClinicalTrials.gov

NCT06416800

Non-Device Trial