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Completed

NCT Number: NCT05817890

Absorption, Metabolism, and Excretion of CYC065 in Healthy Male Subjects

This will be a Phase 1, open-label, single dose study of the Absorption, Metabolism, and Excretion of CYC065 in healthy male subjects.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Early Phase 1

Primary location

Labcorp Clinical Research Unit

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 study site on Day -1 and be confined to the study site until at least Day 8 (168 hours post dose). On Day 1, subjects will receive a single oral dose of [14C]-CYC065. Subjects will be discharged if the following discharge criteria are met: plasma radioactivity levels below the limit of quantitation for 2 consecutive collections, ≥90% mass balance recovery, and ≤1% of the total radioactive dose is recovered in combined excreta (urine and feces) in 2 consecutive 24-hour periods. If discharge criteria are not met by Day 8, subjects will remain in the study site until all discharge criteria are met up to a maximum of Day 15.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Males, of any race, between 18 and 55 years of age, inclusive.
  • Body mass index (BMI) between 18.0 and 32.0 kg/m2, inclusive, with a total body weight ≥50 kg.
  • In good health, determined by no clinically significant findings from medical history, 12-lead electrocardiogram (ECG), vital signs measurements, and clinical laboratory evaluations at screening and check-in and from the physical examination at check-in, as assessed by the investigator (or designee).
  • Males will agree to use contraception.
  • Able to comprehend and willing to sign an ICF and to abide by the study restrictions.
  • History of a minimum of 1 bowel movement per day.

Exclusion criteria

  • Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, or psychiatric disorder, as determined by the investigator (or designee).
  • History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the investigator (or designee).
  • History of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs (uncomplicated appendectomy and hernia repair will be allowed).
  • Confirmed (eg, 2 consecutive measurements) systolic blood pressure >140 mmHg or <90 mmHg, diastolic blood pressure >90 mmHg or <50 mmHg, and pulse rate >100 beats per minute or <40 beats per minute.
  • Positive hepatitis panel and/or positive human immunodeficiency virus test.

Treatment and study plan

Fadraciclib

Drug

Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-CYC065 Following a Single Oral Dose in Healthy Male Subjects

Other names: CYC065

Primary outcomes

  1. The routes, rates of elimination, and mass balance

    Time frame: Up to Day 15

    Total radioactivity from [14C]-CYC065 recovery (fet1t2) in urine and feces

  2. AUC for CYC065 in plasma

    Time frame: Up to Day 15

    To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects

  3. Cmax for CYC065 in plasma

    Time frame: Up to Day 15

    To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects

  4. Tmax for CYC065 in plasma

    Time frame: Up to Day 15

    To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects

  5. t½ for CYC065 in plasma

    Time frame: Up to Day 15

    To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects

Secondary outcomes

  1. Concentration of CYC065 metabolites

    Time frame: Up to Day 15

    To determine, where possible, the quantitative metabolite profiles in plasma, urine, and feces after [14C]CYC065

  2. Incidence and severity of AEs

    Time frame: Up to Day 15

    To assess the safety and tolerability of [14C]CYC065 when administered to healthy subjects

Sponsors and collaborators

Lead sponsor

Cyclacel Pharmaceuticals, Inc.

Industry

Registry information

Official study title

A Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-CYC065 Following a Single Oral Dose in Healthy Male Subjects

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Apr 18, 2023
Registry last updated
Sep 19, 2024

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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