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Completed

NCT Number: NCT04436562

Study of the Absorption, Metabolism, and Excretion Following a Single Dose of [14C]-Poziotinib in Healthy Male Subjects

This will be a Phase 1, open-label, nonrandomized, single-dose study in healthy male subjects to evaluate the Absorption, Metabolism, and Excretion of Poziotinib following a single oral dose of [14C]-poziotinib to healthy male subjects.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Covance Clinical Research Unit, Inc.

Madison, Wisconsin, 53704, United States

About this study

Potential subjects will be screened to assess their eligibility to enter the study within 28 days prior to the dose administration. Subjects will be admitted into the Clinical Research Unit (CRU) on Day -1. On the morning of Day 1, all subjects will receive a single oral dose of 8 mg (as the hydrochloride salt) containing approximately 100 μCi of [14C]-poziotinib in the fasted state.

Subjects will be confined to the CRU until at least Day 8.

Subjects will be discharged from the CRU on Day 8 if the following criteria are met:

  • ≥90% mass balance recovery in combined urine and feces, and
  • ≤1% of the total radioactive dose is recovered in combined excreta (urine and feces) in 2 consecutive 24-hour periods in which fecal and urine samples are obtained.

If these criteria are not met by Day 8, subjects will remain in the CRU until all discharge criteria are met up to a maximum of Day 15 in order to continue 24-hour blood, urine, and feces collections, unless otherwise agreed upon by the Sponsor and Investigator.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • Body mass index between 18.0 and 32.0 kg/m2, inclusive
  • In good health at Screening and/or at Check-in
  • Subjects must be surgically sterile for at least 90 days, or when sexually active with female partners of childbearing and non-childbearing potential will be required to use a male condom with spermicide from CRU Check-in until 90 days after discharge. Subjects are required to refrain from donation of sperm from CRU Check-in until 90 days after discharge
  • Able to comprehend and willing to sign an ICF and to abide by the study restrictions
  • History of at least 1 bowel movement per day

Key Exclusion Criteria:

  • Stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs
  • Swallowing difficulties or ongoing diarrhea of any etiology
  • Participation in a clinical study involving an investigational drug in the past 30 days prior to dosing
  • Use or intend to use any medications/products known to alter drug absorption, metabolism, or elimination processes, including St. John's wort, within 30 days prior to Check-in
  • Use or intend to use any prescription medications/products within 14 days prior to Check-in
  • Use or intend to use slow-release medications/products considered to still be active within 14 days prior to Check-in
  • Exposure to significant diagnostic or therapeutic radiation or current employment in a job requiring radiation exposure monitoring within 12 months prior to Check-in

Treatment and study plan

[14C]-Poziotinib

Drug

Single oral administration of 8 mg (as the hydrocholoride salt) of [14C]-poziotinib

Primary outcomes

  1. Maximum Observed Plasma Concentration (Cmax) of [14C]-Poziotinib, Metabolites M1 and M2

    Time frame: 1-15 days

  2. Cmax of Total Radioactivity of [14C]-Poziotinib in Whole Blood and Plasma

    Time frame: 1-15 days

  3. Time to Attain Maximum Observed Plasma Concentration (Tmax) of [14C]-Poziotinib, Metabolites M1 and M2

    Time frame: 1-15 days

  4. Tmax of Total Radioactivity of [14C]-Poziotinib in Whole Blood and Plasma

    Time frame: 1-15 days

  5. Area Under the Plasma Concentration-Time Curve From Time Zero to Last Quantifiable Concentration (AUC[last]) of [14C]-Poziotinib, Metabolites M1 and M2

    Time frame: 1-15 days

  6. AUC(last) of Total Radioactivity of [14C]-Poziotinib in Whole Blood and Plasma

    Time frame: 1-15 days

  7. Area Under the Plasma Concentration-Time Curve From Time Zero to Infinity (AUCinf) of [14C]-Poziotinib, Metabolites M1 and M2

    Time frame: 1-15 days

  8. AUC(inf) of Total Radioactivity of [14C]-Poziotinib in Whole Blood and Plasma

    Time frame: 1-15 days

  9. Percentage of AUCinf Derived by Extrapolation (%AUCext) of [14C]-Poziotinib, Metabolites M1 and M2

    Time frame: 1-15 days

  10. %AUCext of Total Radioactivity of [14C]-Poziotinib in Whole Blood and Plasma

    Time frame: 1-15 days

  11. Apparent Terminal Elimination Half-Life (t1/2) of [14C]-Poziotinib, Metabolites M1 and M2

    Time frame: 1-15 days

  12. t1/2 of Total Radioactivity of [14C]-Poziotinib in Whole Blood and Plasma

    Time frame: 1-15 days

  13. Elimination Rate Constant (λz, or kel) of [14C]-Poziotinib, Metabolites M1 and M2

    Time frame: 1-15 days

  14. λz, or kel of Total Radioactivity of [14C]-Poziotinib in Whole Blood and Plasma

    Time frame: 1-15 days

  15. Apparent Volume of Distribution (VZ/F) During Terminal Phase of [14C]-Poziotinib

    Time frame: 1-15 days

  16. Apparent Oral Clearance (CL/F) of [14C]-Poziotinib

    Time frame: 1-15 days

  17. Whole Blood : Plasma Concentration Ratios of Total Radioactivity of [14C]-Poziotinib

    Time frame: 1-15 days

  18. Total Radioactivity of Cumulative Amount Excreted in Urine (Aeu)

    Time frame: 1-15 days

  19. Total Radioactivity of Fraction of Dose Excreted in Urine (feu)

    Time frame: 1-15 days

  20. Total Radioactivity of Cumulative Amount Excreted in Feces (Aef)

    Time frame: 1-15 days

  21. Total Radioactivity of Fraction of Dose Excreted in Feces (fef)

    Time frame: 1-15 days

  22. Total Radioactivity of Cumulative Total Amount Excreted (Aetotal)

    Time frame: 1-15 days

  23. Total Radioactivity of Fraction of Dose Excreted in Urine and Feces (fetotal)

    Time frame: 1-15 days

  24. Poziotinib Metabolite Profiling and Identification in Plasma

    Time frame: 1-15 days

Secondary outcomes

  1. Number of Participants with Adverse Events (AEs)

    Time frame: 1-15 days

  2. Number of Participants with Hematology, Clinical Chemistry, Urinalysis Laboratory Abnormalities

    Time frame: 1-15 days

  3. Number of Participants with 12-lead electrocardiograms (ECG) Abnormalities

    Time frame: 1-15 days

  4. Number of Participants with Vital Sign and Physical Examinations Abnormalities

    Time frame: 1-15 days

Sponsors and collaborators

Lead sponsor

Spectrum Pharmaceuticals, Inc

Industry

Registry information

Official study title

Phase 1 Open-label Study of the Absorption, Metabolism, and Excretion of Poziotinib Following a Single Oral Dose of [14C]-Poziotinib in Healthy Male Subjects

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jun 18, 2020
Registry last updated
Jan 15, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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