A Study to Evaluate the Relative Bioavailability of New Formulations of INCB057643 Tablets Administered Orally in Healthy Participants

Relative Bioavailability of New Formulations of INCB057643 Tablets Administered Orally in Healthy Participants

The purpose of this study is to evaluate the Relative Bioavailability of New Formulations of INCB057643 Tablets Administered Orally in Healthy Participants.

Study Overview

• Status: Completed
• Conditions: Healthy Volunteers
• Intervention / Treatment: Drug: INCB057643

• Study Type: Interventional
• Enrollment (Actual): 48
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Arizona
    • Tempe, Arizona, United States, 85283
      • Celerion, Inc

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Ability to comprehend and willingness to sign a written ICF for the study.
• Aged 18 to 55 years, inclusive, at the time of signing the ICF.
• BMI within the range of 18.0 to 30.0 kg/m2 inclusive. Note: Up to 25% of the participants in each cohort may be enrolled with a BMI > 30 to ≤ 32.0 kg/m2.
• No clinically significant findings on screening evaluations (clinical, laboratory, and ECG).
• Ability to swallow and retain oral medication.

Exclusion Criteria:

• History of uncontrolled or unstable respiratory, renal, GI, endocrine, hematopoietic, psychiatric, and/or neurological disease within 6 months of screening.
• History of cardiovascular, cerebrovascular, peripheral vascular, or thrombotic disease or uncontrolled hypertension.
• High blood pressure (systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg at screening, confirmed by repeat testing).
• History or presence of an abnormal ECG before screening and check-in that, in the investigator's opinion, is clinically significant, such as a QTcF interval > 450 milliseconds, QRS interval > 120 milliseconds, or PR interval > 220 milliseconds.
• History or presence of a malabsorption syndrome possibly affecting drug absorption (eg, Crohn disease or chronic pancreatitis).
• Hepatic transaminases (ALT and AST), ALP, or total bilirubin > 1.25 × the laboratory-defined ULN at screening and check-in, confirmed by repeat testing (except participants with Gilbert disease, for which total bilirubin must be ≤ 2.0 × ULN).
• Any major surgery within 4 weeks of screening.
• Current or recent (within 3 months of screening) clinically significant GI disease or surgery (including cholecystectomy and excluding appendectomy) that could affect the absorption of study drug.
• Donation of blood to a blood bank or participation in a clinical study (except a screening visit) within 4 weeks of screening (within 2 weeks for donation of plasma only).
• Positive test for HBV, HCV, or HIV. Participants whose results are compatible with prior immunization for or immunity due to infection with HBV may be included at the discretion of the investigator.
• History of significant alcohol use, defined as regular alcohol consumption > 21 units per week for males and > 14 units for females (1 unit = 8 ounces of beer or a 25-mL shot of 40% spirit, 1.5 to 2 units = 125-mL glass of wine, depending on type).
• Positive urine or breath test for ethanol or positive urine or serum screen for drugs of abuse that are not otherwise explained by permitted concomitant medications or diet.
• Current treatment or treatment within 30 days or 5 half-lives (whichever is longer) before the first dose of study drug with another investigational medication or current enrollment in another investigational drug or investigational product study.
• History of tobacco or nicotine-containing product use within 1 month of screening.
• Use of prescription drugs (including hormonal contraceptives) within 14 days of study drug administration or nonprescription medications/products (including vitamins, minerals, and phytotherapeutic/herbal/plant-derived preparations) within 7 days of study drug administration. However, occasional and standard-dose acetaminophen and ibuprofen and standard-dose vitamins are permitted. Megadose vitamins or supplements are not permissible.

Other protocol-defined Inclusion/Exclusion Criteria may apply.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: None (Open Label)

Number of Arms

5

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Cohort 1: Dose Treatment A; INCB057643 will be administered at protocol defined dose.	Drug: INCB057643; Tablet
Experimental: Cohort 2: Dose Treatment B; INCB057643 will be administered at protocol defined dose.	Drug: INCB057643; Tablet
Experimental: Cohort 3: Dose Treatment C; INCB057643 will be administered at protocol defined dose.	Drug: INCB057643; Tablet
Experimental: Cohort 4: Dose Treatment D; INCB057643 will be administered at protocol defined dose.	Drug: INCB057643; Tablet
Experimental: Cohort 4: Dose Treatment E; INCB057643 will be administered at protocol defined dose.	Drug: INCB057643; Tablet

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pharmacokinetics Parameter (PK): Cmax of INCB057643	Defined as maximum observed plasma concentration of INCB057643.	Up to Day 10
Pharmacokinetics Parameter: AUC(0-last) of INCB057643	Defined as area under the single-dose serum concentration-time curve from time = 0 to the last measurable concentration at time of INCB057643.	Up to Day 10
Pharmacokinetics Parameter: AUC 0-∞ of INCB057643	Defined as the area under the single-dose serum concentration-time curve extrapolated to time of infinity of INCB057643.	Up to Day 10

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with Treatment-emergent Adverse Events (TEAEs)	Defined as adverse events reported for the first time or worsening of a pre-existing event after first dose of study drug.	Up to Day 26
Pharmacokinetics Parameter: Tmax of INCB057643	Defined as the time to reach the maximum plasma concentration of INCB057643.	Up to Day 10
Pharmacokinetics Parameter: t1/2 of INCB057643	Defined as the apparent terminal phase disposition half-life of INCB057643.	Up to Day 10
Pharmacokinetics Parameter: CL/F INCB057643	Defined as the apparent oral dose clearance of INCB057643.	Up to Day 10
Pharmacokinetics Parameter: V2/F of INCB057643	Defined as the apparent oral dose volume of distribution of INCB057643.	Up to Day 10
Pharmacokinetics Parameter: λz of INCB057643	Defined as apparent terminal-phase disposition rate constant of INCB057643.	Up to Day 10
Pharmacokinetics Parameter: %AUCexp of INCB057643	Defined as percentage of AUC0-∞ due to extrapolation from the time of last quantifiable concentration to infinity of INCB057643.	Up to Day 10

Collaborators and Investigators

• Sponsor: Incyte Corporation
• Investigators: Study Director: Incyte Study Monitor, Incyte Corporation

Publications and helpful links

Helpful Links

• A Study to Evaluate the Relative Bioavailability of New Formulations of INCB057643 Tablets Administered Orally in Healthy Participants

Study record dates

Study Major Dates

• Study Start (Actual): May 12, 2025
• Primary Completion (Actual): June 3, 2025
• Study Completion (Actual): June 3, 2025

Study Registration Dates

• First Submitted: April 16, 2025
• First Submitted That Met QC Criteria: April 16, 2025
• First Posted (Actual): April 23, 2025

Study Record Updates

• Last Update Posted (Actual): June 11, 2025
• Last Update Submitted That Met QC Criteria: June 10, 2025
• Last Verified: June 1, 2025

More Information

Terms related to this study

• Keywords: INCB057643
• Additional Relevant MeSH Terms: Antineoplastic Agents; INCB057643
• Other Study ID Numbers: INCB057643-111

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No