A Mass Balance Study of DZD8586 in Healthy Male Participants (TAI-SHAN15)

A Phase I, Single-center, Non-randomized, Open-label, Mass Balance Study of Orally Administered [14C]-DZD8586 in Healthy Adult Male Participants

This phase I study is designed to evaluate absorption, metabolism and excretion (AME) profiles of [14C]-DZD8586, to determine the routes, rates of elimination, and mass balance of DZD8586 in healthy adult male participants. Participants will be administered a single oral dose of 50 mg of [14C]-DZD8586 (containing radioactive dose ~ 100 μCi) as a suspension.

Study Overview

• Status: Completed
• Conditions: Lymphoma, Non-Hodgkin
• Intervention / Treatment: Drug: DZD8586

• Study Type: Interventional
• Enrollment (Actual): 6
• Phase: Phase 1

Contacts and Locations

Study Locations

• China
  • Jiangsu
    • Wuxi, Jiangsu, China, 214062
      • Affiliated Hospital of Jiangnan University

Participation Criteria

Eligibility Criteria

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

Description

Inclusion Criteria:

Each participant must meet all criteria below to be included in this study:

1. Provision of signed and dated, written informed consent prior to any study-specific procedures.
2. Healthy male volunteers aged 18 to 45 years (inclusive) with a body mass index (BMI) between 19 and 26 kg/m2(inclusive) and body weight > 50 kg.
3. The results of physical examination, laboratory tests, chest X-ray (posteroanterior view), electrocardiogram, and/or other auxiliary examinations (including abdominal ultrasound of the liver, gallbladder, pancreas, spleen, and kidneys; ophthalmologic examination; and digital rectal examination) are within normal results during the screening period or abnormal results with no clinical significance judged by the investigator.
4. Male volunteers must be willing to use reliable methods of contraception (condom) even if their partners are postmenopausal, surgically sterile, or using an effective hormonal method of contraception or intrauterine coil. In addition, volunteers must agree to continue to take similar contraceptive precautions through 12 months after the administration of DZD8586, and avoid procreative sex as well as sperm donation during this period.
5. Be willing and able to comply with the study procedures, restrictions, and requirements.

Exclusion Criteria:

Each participant who meets any of the criteria below will be excluded from this study:

1. Abnormalities in vital signs assessment (including pulse, blood pressure, and tympanic temperature) that persist upon repeat measurement.

2. History or current cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study intervention; or interfering with the interpretation of data.

   For gastrointestinal function, the patient who meets the criteria below should be excluded:

   • History or clinical manifestation of gastritis, gastrointestinal tract disorder, metabolic disorder, hepatic disorder, or other clinical condition
   • Nausea, vomiting, diarrhea, or malabsorption syndrome, or those with a history of severe vomiting or diarrhea within one week before the screening period.
   • Abnormal bowel movements (ie, on average production of less than 1 stool per day) or other gastrointestinal disorder that might affect the intake and absorption of the drug, as judged by the investigator.
   • Symptomatic hemorrhoids or perianal disease with regular/active rectal bleeding, irritable bowel syndrome, or inflammatory bowel disease during the screening period.
3. History of other risk factors for TdP (such as heart failure, hypokalemia, and family history of long QT syndrome).
4. During the screening period, the average resting corrected QTcF interval (QTC) on the ECG is > 450 msec.
5. Major surgery or severe trauma within 4 weeks before the screening, or scheduled surgery during the study period.
6. History of hemorrhagic disease (including hemophilia, von Willey-Brandland disease, etc), stroke, or intracranial hemorrhage within 6 months prior to the screening.
7. Blood donation (including blood products) or blood loss ≥ 500 mL within 2 months prior to the screening, or receiving blood products within 4 weeks prior to the screening.
8. Participants with any malignancy or neoplastic disease history, except those who have undergone excisional surgery of non-melanoma skin cancer over 5 years prior to the screening.
9. History of latent or active tuberculosis, or positive screening result.
10. Bacterial infection (including) within 30 days prior to the screening is considered inappropriate for participation by the investigator.
11. Any infection on screening tests for Treponema pallidum, Hepatitis B Virus (HBsAg and HBcAb), Hepatitis C Virus (HCV), or human immunodeficiency virus (HIV-Ag/Ab).
12. History of severe allergy/hypersensitivity or ongoing allergy/hypersensitivity, or those who are known or suspected to be allergic to the investigational product or any of its excipients, as judged by the investigator.
13. Has smoked an average of more than 5 cigarettes per day within the 3 months prior to screening, is a habitual user of nicotine-containing products, is unable to abstain from smoking/nicotine use during the trial period, or has a positive urine cotinine test.
14. Has a known or suspected history of significant drug abuse (including licit or illicit drugs, alcohol, etc.) within 12 months prior to screening as judged by the investigator, a positive alcohol breath test result (>0 mg/100 mL) at screening, or a positive urine drug abuse screening test.
15. Use of any prescribed medication within 4 weeks prior to the screening and refuse to restrict the use of prescription drugs Use or intention to use any prescription or over-the-counter medications (including but not limited to moderate to strong CYP3A4/5P inhibitor or inducers [including herbal products such as St. John's wort], any ADH and ALDH inhibitor/inducers, proton pump inhibitors, antacids, H2 receptor antagonists, and drugs that prolong QT/QTc interval, herbal products, natural or herbal supplements) within 4 weeks prior to the screening and through the end of the study, unless deems acceptable by the Investigator (or designee) and Sponsor.
16. Participants who received live or live-attenuated vaccine in the 4 weeks prior to the screening (or related AEs haven't disappeared).
17. Has participated in other clinical trials and received any investigational product or device within 3 months prior to the screening, plans to participate in another clinical trial during this study, or is not the actual personnel participating in the trial.
18. Participants monitored for radiation exposure as part of their occupation.
19. Radioactive exposure (≥2 times chest/abdominal CT scans, or ≥3 times other types of X-ray examinations) or those who have participated in radiopharmaceutical labelling tests within one year before the screening period.
20. Participants who had been administered any amount of a [14C]-labelled compound within 12 months prior to the screening.
21. History of vasovagal response to needles or blood, difficult venous access, or intolerance to venipuncture.
22. Judgment by the investigator that the volunteer is not suitable to participate in the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Carbon-14 labeled DZD8586; Single oral administration of Carbon-14 labeled DZD8586 50 mg/100 μCi on empty stomach	Drug: DZD8586; Carbon-14 labeled DZD8586

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Total amount and recovery of the radioactive dose in urine and feces: Ae, Cum Ae, fe and Cum fe	All excreted urine and feces samples at specified time points during 0-504 hours after dosing will be collected
Metabolic profiling of relative abundance of [14C]-DZD8586 and metabolite identification of [14C]-DZD8586 in plasma, urine, and feces	Conduct testing within 1 month after all subjects collect plasma, urine, and fecal samples at all time points required by the protocol

Secondary Outcome Measures

Outcome Measure	Time Frame
Peak plasma concentration (Cmax) of DZD8586	up to 504 hours post dose
Peak plasma concentration (Cmax) of DZ4581	up to 504 hours post dose
Peak concentration (Cmax) of total radioactivity concentration equivalents in plasma and whole blood	Conduct testing within 1 month after all subjects collect whole blood and plasma samples at all time points defined by the protocol
Time to Cmax (Tmax) of DZD8586	up to 504 hours post dose
Time to Cmax (Tmax) of DZ4581	up to 504 hours post dose
Time to Cmax (Tmax) of total radioactivity concentration equivalents in plasma and whole blood	Conduct testing within 1 month after all subjects collect whole blood and plasma samples at all time points defined by the protocol
Elimination half-life (t1/2,λz) of DZD8586	up to 504 hours post dose
Elimination half-life (t1/2,λz) of DZ4581	up to 504 hours post dose
Elimination half-life (t1/2,λz) of total radioactivity concentration equivalents in plasma and whole blood	Conduct testing within 1 month after all subjects collect whole blood and plasma samples at all time points required by the protocol
Area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC0-t) of DZD8586	up to 504 hours post dose
Area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC0-t) of DZ4581	up to 504 hours post dose
Area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC0-t) of total radioactivity concentration equivalents in plasma and whole blood	Conduct testing within 1 month after all subjects collect whole blood and plasma samples at all time points required by the protocol
Area under the concentration-time curve from time zero to infinity (AUC0-inf) of DZD8586	up to 504 hours post dose
Area under the concentration-time curve from time zero to infinity (AUC0-inf) of DZ4581	up to 504 hours post dose
Area under the concentration-time curve from time zero to infinity (AUC0-inf) of total radioactivity concentration equivalents in plasma and whole blood	Conduct testing within 1 month after all subjects collect whole blood and plasma samples at all time points required by the protocol
Apparent oral clearance (CL/F) of DZD8586	up to 504 hours post dose
Apparent volume of distribution (Vz/F) of DZD8586	up to 504 hours post dose
PK parameters for renal clearance (CLR) for DZD8586 and DZ4581 in urine	up to 504 hours post dose
Amount and percentage of DZD8586 recovered in urine	up to 504 hours post dose
Plasma DZD8586-to-total plasma radioactivity ratio	Conduct testing within 1 month after all subjects collect plasma samples at all time points required by the protocol
Whole blood to plasma total radioactivity ratio	Conduct testing within 1 month after all subjects collect whole blood and plasma samples at all time points required by the protocol
Frequency, type and severity of adverse events/serious adverse events	Up to 3 weeks
Pulse rate	Up to 3 weeks
Blood pressure	Up to 3 weeks
Heart rate	Up to 3 weeks
RR, PR, QRS, and QT intervals	Up to 3 weeks
Number of participants with abnormal laboratory tests results (including blood chemistry, hematology, coagulation function, and urinalysis)	Up to 3 weeks
Number of participants with abnormal physical and ophthalmologic examinations findings	Up to 3 weeks

Collaborators and Investigators

• Sponsor: Dizal Pharmaceuticals
• Investigators: Principal Investigator: Yiqing Zhao, Affiliated Hospital of Jiangnan University

Study record dates

Study Major Dates

• Study Start (Actual): March 16, 2026
• Primary Completion (Actual): March 27, 2026
• Study Completion (Actual): April 6, 2026

Study Registration Dates

• First Submitted: January 26, 2026
• First Submitted That Met QC Criteria: March 2, 2026
• First Posted (Actual): March 6, 2026

Study Record Updates

• Last Update Posted (Actual): May 14, 2026
• Last Update Submitted That Met QC Criteria: May 13, 2026
• Last Verified: May 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms; Immune System Diseases; Neoplasms by Histologic Type; Lymphatic Diseases; Lymphoproliferative Disorders; Immunoproliferative Disorders; Lymphoma; Hemic and Lymphatic Diseases; Lymphoma, Non-Hodgkin
• Other Study ID Numbers: DZ2025B0003

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