A Mass Balance Study to Investigate the Absorption, Metabolism, and Excretion Of [14C] Fruquintinib

Phase 1

Completed

• Conditions: Healthy
• Interventions: Drug: fruquintinib

• Registration Number: NCT02689752
• Lead Sponsor: Hutchison Medipharma Limited

Brief Summary

This will be an open-label, single-center study to evaluate pharmacokinetics and safety of HMPL-013 in approximately 6 healthy male subjects receiving a single oral 5mg dose of HMPL-013 containing approximately 100 microcuries of \[14C\] HMPL-013. This study will investigate the absorption, drug biotransformation and mass balance of HMPL-013, seek to identify the compound's major metabolites and supply information for clinical application.

Detailed Description

This study will be an open-label, mass balance study of fruquintinib administered orally at 5mg (100mCi). Subjects will be screened for eligibility up to 14 days prior to entry into the study. For study period, subjects will be admitted to the clinical research unit (CRU) on the day before dosing and fast overnight (approximately 10 hours). On the morning of dosing for study period, subjects will receive a single oral dose of 5 mg fruquintinib in the fasted state. Subjects will remain at the CRU for at least 336 hours after administration of study drug for collection of serial blood samples for pharmacokinetic (PK) analysis and safety monitoring.

Study Timeline

• Study First Submitted: 2016-02-03
• Study First Submitted QC: 2016-02-18
• Study First Posted: 2016-02-24
• Study Start: 2016-07
• Primary Completion: 2016-09
• Study Completion: 2016-09
• Status Verified: 2020-02
• Last Update Submitted: 2020-02-12
• Last Update Posted: 2020-02-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 6

Inclusion Criteria

1. A Healthy Male Volunteer between 18 and 40 years of age inclusive;
2. A Body Mass Index (BMI) within the range of 19 to 25 kg/m2 and a total body weight >50kg;
3. Medically normal subjects with no significant abnormal findings at the screening vital signs, physical examination, electrocardiogram (ECG), and laboratory parameters as evaluated by the investigator;
4. Fertile male subjects and their partners are willing to undergo contraception as follows: condom, contraceptive sponge, contraceptive gel, contraceptive diaphragm, intrauterine devices, hormonal contraceptives (oral or injectable), subepidermal contraceptive implant and other contraception methods during the study and until 1 year after taking the dose of investigational product,
5. Subject must voluntarily consent to participate in this study, provide their written informed consent prior to start of any study- specific procedures and be willing to comply with all study procedures.

Exclusion Criteria

1. Subjects who have a family history of coronary heart disease;
2. Subjects who have a known history of bleeding such as gingival hemorrhage, epistaxis and hemorrhoid bleeding etc.;
3. Subjects have hypertension (Systolic Pressure ≥140 mmHg or Diastolic Pressure ≥90 mmHg);
4. Subjects who are taking, or have taken any drugs that affect metabolism or prescription medication during the screening or within 30 days prior to the screening; Subjects who are taking, or have taken any OTC, herbal remedies or Vitamin during the screening or within 14 days prior to the screening; Subjects who are taking, or have taken any plant extracts like Hypericum Perforatum L. which are not therapeutic but have health function and can affect the absorption and metabolism during the screening or within 3 days prior to the screening; Subjects who have participated in another clinical trial within 2 months prior to the screening;
5. Subjects who are taking, or have taken any drugs which have toxicity to major organs during the screening or within 3 months prior to the screening;
6. Subjects who test positive for nicotine screening or can't quit smoking completely in the study;
7. Subjects who have history or presence of any clinically significant diseases within 3 months prior to the screening;
8. Subjects who have history or presence of gastrointestinal, hepatic, renal diseases or any other known condition that can affect the absorption, distribution, metabolism or excretion of the investigational product;
9. Subjects who have chronic constipation, diarrhea, irritable bowel syndrome or inflammatory bowel disease;
10. Subjects who have hemorrhoids or perianal complications with regular hematochezia;
11. Subjects who have a known history of severe allergic reaction such as drug allergy or had an acute allergic rhinitis or food allergy within 14 days prior to the study medication;
12. Subjects who have donated blood or plasma more than 500ml within 2 months prior to the study medication or more than 50ml within 14 days prior to the study medication;
13. Subjects who have had a positive test for hepatitis B (HBsAg) or hepatitis C (excluded immunization);
14. Subjects who have had a positive test for human immunodeficiency virus (HIV);
15. Subjects who have taken vaccination during the screening or within 6 months prior to the screening;
16. Subjects who have any prior history of substance abuse or treatment (including alcohol) ;
17. Subjects who can't understand the purpose, extent and possible outcomes of the study because of mental disease;
18. Adult subjects who are imprisoned or whose freedom are restricted because of administrative problem or legal issues;
19. Subjects who can't comply with the protocol such as discontinue the follow-up and finish the study according to the protocol;
20. Subjects who are involved in the study design and proceeding such as investigator, pharmacist, clinical research coordinator or other related personnel;
21. Subjects who have any other unsuitable or adverse condition to be determined by the investigator;
22. Subjects who have participated in a radiolabeled clinical trial prior to study medication;
23. Subjects who have been exposed to significant radiation (e.g., x-ray investigation, CT investigation, more than one time radiation exposure in barium meal examination) or whose occupation requires exposure to radiation in the last 12 months.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
fruquintinib	fruquintinib	fruquintinib suspension, 5 mg （100 mCi）oral taken once

Primary Outcome Measures

Name	Time	Method
Total radioactivity on blood, urine and faeces (radiocarbon) following oral suspension [14C]HMPL-013 dosing	Up to 14 days	Total radioactivity in blood to determine Cmax, Tmax, Half-life, AUC0-t, AUC0-∞ Total radioactivity in urine and faeces at each time interval and cumulative radioactivity (mass balance)

Secondary Outcome Measures

Name	Time	Method
Blood concentrations of HMPL-013 and its metabolites	Up to 14 days	Blood concentrations of HMPL-013 and its metabolites to determine Cmax, Tmax, Half-life, AUC0-t, AUC0-∞
Mass balance after a single oral dose of [14C] HMPL-013 as generated from recovery of total radioactivity excreted in urine and faeces.	Up to 14 days
Metabolite profililing and identification of metabolites in blood, urine and faeces	up to 14 days
Safety and tolerability parameters, including adverse events (AEs), vital signs, ECGs, and clinical laboratory assessments.	Up to 14 days	safety will assessed by physical exam, clinical laboratory evaluations and ECGs.

Trial Locations

Locations (1)

Jiangsu Province Hospital; 🇨🇳 Nanjing, Jiangsu, China