Labcorp Clinical Research Unit
Madison, Wisconsin, 53704, United States
NCT Number: NCT05817890
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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Notify Me18 year–55 year
Male
Interventional
Early Phase 1
Madison, Wisconsin, 53704, United States
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-CYC065 Following a Single Oral Dose in Healthy Male Subjects
Other names: CYC065
Time frame: Up to Day 15
Total radioactivity from [14C]-CYC065 recovery (fet1t2) in urine and feces
Time frame: Up to Day 15
To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects
Time frame: Up to Day 15
To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects
Time frame: Up to Day 15
To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects
Time frame: Up to Day 15
To characterize the PK of CYC065 and total radioactivity following administration of [14C]CYC065 to healthy subjects
Time frame: Up to Day 15
To determine, where possible, the quantitative metabolite profiles in plasma, urine, and feces after [14C]CYC065
Time frame: Up to Day 15
To assess the safety and tolerability of [14C]CYC065 when administered to healthy subjects
Cyclacel Pharmaceuticals, Inc.
Industry
A Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-CYC065 Following a Single Oral Dose in Healthy Male Subjects
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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