Single Dose Mass Balance Study With [14C]Iruplinalkib (WX-0593) In Healthy Male Volunteers

NCT05716126 | Completed Phase 1 FDA Drug

• 1 other identifier: WX0593-005
• Study Type: interventional
• Target: 6
• Locations: 1 country
• Sites: 1

Brief Summary

This is an open-label, single dose, mass balance and biotransformation study conducted at 1 study center in China. This study will evaluate the absorption, distribution, metabolism, and elimination (ADME), mass balance, safety, and tolerability of a single dose of intravenously administered \[14C\]Iruplinalkib (WX-0593) in Chinese healthy male volunteers.

Conditions

Healthy

Outcome Measures

Primary Outcomes (5)

• Metabolic profiling for iruplinalkib(WX-0593) will be determined in plasma samples.

  Percent (%) of each radiolabeled drug-related material (parent and each metabolite) will be determined in plasma, urine and feces.

  Assessments will be made up to 3 days post dose.

• Metabolic profiling for iruplinalkib(WX-0593) will be determined in urine samples.

  Percent (%) of each radiolabeled drug-related material (parent and each metabolite) will be determined in urine.

  Assessments will be made up to 3 days post dose.

• metabolic profiling for iruplinalkib(WX-0593) will be determined in fecal samples.

  Percent (%) of each radiolabeled drug-related material (parent and each metabolite) will be determined in feces.

  Assessments will be made up to 3 days post dose.

• Total Radioactivity in Feces

  Cumulative amount was calculated as sum of feces drug concentration in sample volume for each collection interval.

  Assessments will be made up to 14 days post dose.

• Total Radioactivity in Urine

  Cumulative amount was calculated as sum of urine drug concentration in sample volume for each collection interval.

  Assessments will be made up to 14 days post dose.

Secondary Outcomes (1)

• Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs)

  Assessments will be made up to 28 days post dose.

Study Arms (1)

[14]Iruplinalkib(WX-0593) 120 mg(orla solution)

EXPERIMENTAL

Volunteer will receive a single oral dose of 120 mg \[14C\]Iruplinalkib (WX-0593) administered by mouth, as a solution.

Drug: [14C]Iruplinalkib (WX-0593)

Interventions

[14C]Iruplinalkib (WX-0593) DRUG

Volunteer will receive a single oral dose of 120 mg \[14C\]Iruplinalkib (WX-0593) as a solution on Day 1

[14]Iruplinalkib(WX-0593) 120 mg(orla solution)

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• years old (inclusive) healthy male volunteers;
• Body mass index 19.0-26.0 kg/m 2 (inclusive) and body weight ≥50 kg;
• The volunteer has fully given informed consent to the study and voluntarily signed the informed consent form prior to trial.

You may not qualify if:

• Physical examination, vital signs, laboratory tests (routine blood test, urinalysis, stool + occult blood test, blood biochemistry, blood coagulation, and thyroid function), ophthalmic examination (slit lamp exam, intraocular pressure, and fundus imaging), 12-lead electrocardiogram, chest X-ray (posteroanterior view), and abdominal ultrasound results that are determined abnormal and clinically significant by the investigator during screening;
• Positive for HBsAg, HBeAg, HCV antibody, HIV antibody, or syphilis antibody;
• Has taken any prescribed medication and herbal medicine within 1 month prior to dosing, or has taken over-the-counter medications or food supplements (e.g. Vitamins or calcium) within 2 months prior to dosing;
• Has participated in clinical trials of any other drug within 3 months prior to dosing;
• Previous heart disease or family history of heart disease, such as organic heart disease, heart failure, myocardial infarction, angina, irreducible arrhythmia, torsades de pointes, ventricular tachycardia, or long QT syndrome;
• Major surgery within 6 months prior to dosing or surgical incision is not completely healed; Major surgery includes but is not limited to surgery with any significant risk of bleeding, prolonged general anesthesia, biopsy or significant traumatic injury;
• Any history of severe clinical illness or disease and conditions that are judged by the investigator to potentially affect the results of the study or disease and history of disease that can reduce treatment adherence (including but not limited to cardiovascular, liver, kidney, gastrointestinal, immune, urinary, blood, endocrine, metabolic, mental, and neurological diseases as well as cancer), especially a history of dysphagia, gastrointestinal ulcers or any gastrointestinal disorders that affect drug absorption;
• Known allergy to two or more substances; Or potential allergy to the test drug or its excipients in the judgment of the investigator, or allergy to any food ingredients, or special requirements for diet and inability to consume a uniform diet;
• Hemorrhoids or perianal disease with regular/current bleeding;
• Habitual constipation, diarrhea, irritable bowel syndrome, or inflammatory bowel disease;
• Consumed over 14 units of alcohol (1 unit = 360 mL beer or 45 mL of liquor with 40% alcohol or 150 mL wine) weekly within 6 months prior to screening or breath alcohol test result of ≥20 mg/dL;
• Consumed more than 5 cigarettes daily within 3 months prior to screening or inability to quit smoking during the study;
• Consumed soft drugs (e.g. Marijuana, MDMA, ketamine or magu/yaba) within 3 months prior to dosing or hard drugs (E.g. Cocaine, heroin, or methamphetamine) within 1 year prior to dosing or positive for urine drug test;
• Habitually consumed grapefruit or grapefruit juice, or excessively consumed tea, coffee, alcohol and/or drinks containing caffeine or alcohol and unable to quit during hospitalization, or frequent strenuous exercise and other factors that affect drug absorption, distribution, metabolism, and excretion;
• Consumed any food or drink rich in xanthine (e.g. Animal organs, chocolate, tea, coffee or coke) within 48 hr prior to dosing, or any grapefruit or products containing grapefruit within 48 hr prior to dosing;

Sponsors & Collaborators

• Qilu Pharmaceutical Co., Ltd.: lead

Study Sites (1)

The First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, 215006, China

Location

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 27, 2023
• First Posted: February 8, 2023
• Study Start: April 15, 2020
• Primary Completion: December 15, 2020
• Study Completion: January 13, 2021
• Last Updated: February 8, 2023

Record last verified: 2023-02

Locations

CN (1)