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To Evaluate the Safety, Tolerability, and Pharmacokinetics of YG1699（Antidiabetic） in Healthy Chinese Sbjects

Sponsor
Youngene Therapeutics Inc., Ltd. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05089617
Collaborator
(none)
20
Enrollment
1
Location
3
Arms
3.8
Anticipated Duration (Months)
5.2
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a randomized, double-blind, placebo-controlled, single ascending dose (SAD) and multi-dose, sequential, bridging study in healthy volunteer using YG1699 .

Condition or Disease Intervention/Treatment Phase
Phase 1

Detailed Description

This is a randomized, double-blind, placebo-controlled, dose-ascending study to evaluate the safety, tolerability, and pharmacokinetics (PK) of YG1699 following single ascending and multiple oral dose administration.

The study consists of 2 parts: Part 1, SAD dose- ascending; Part 2, multi-dose ascending.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Intervention Model Description:
Single Ascending Dose and Multiple DoseSingle Ascending Dose and Multiple Dose
Masking:
Triple (Participant, Care Provider, Investigator)
Masking Description:
Double Blinded
Primary Purpose:
Treatment
Official Title:
To Evaluate the Safety, Tolerability, and Pharmacokinetics of Oral Administration of YG1699 in Healthy Chinese Subjects: a Randomized, Double-blind, Placebo-controlled, Single Ascending Dose (SAD) and Multi-dose, Sequential, Bridging Study
Actual Study Start Date :
Jan 9, 2022
Anticipated Primary Completion Date :
Mar 21, 2022
Anticipated Study Completion Date :
May 5, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: SAD Cohort 1

5 mg YG1699 or Placebo

Drug: YG1699
YG1699 is a novel investigational dual inhibitor of sodium-dependent glucose cotransporters, SGLT1 and SGLT2, indicated as an adjunct to diet and exercise to improve glycemic control and weight loss in adults with T2DM. A subsequent indication will be developed for YG1699 to improve glycemic control in adults with T1DM. Drug: Placebo Placebo is the same appearance as YG1699.
Experimental: SAD Cohort 2

25 mg YG1699 or Placebo

Drug: YG1699
YG1699 is a novel investigational dual inhibitor of sodium-dependent glucose cotransporters, SGLT1 and SGLT2, indicated as an adjunct to diet and exercise to improve glycemic control and weight loss in adults with T2DM. A subsequent indication will be developed for YG1699 to improve glycemic control in adults with T1DM. Drug: Placebo Placebo is the same appearance as YG1699.
Experimental: Multiple Doses Cohort 1

20 mg YG1699 or Placebo

Drug: YG1699
YG1699 is a novel investigational dual inhibitor of sodium-dependent glucose cotransporters, SGLT1 and SGLT2, indicated as an adjunct to diet and exercise to improve glycemic control and weight loss in adults with T2DM. A subsequent indication will be developed for YG1699 to improve glycemic control in adults with T1DM. Drug: Placebo Placebo is the same appearance as YG1699.

Outcome Measures

Primary Outcome Measures

  1. Adverse events will be evaluated [81 Days]

    Safety and Tolerability of YG1699

Secondary Outcome Measures

  1. Area Under the Curve [AUC] [81 Days]

    area under the plasma drug concentration time curve from time 0 to T (AUC)

  2. maximum plasma concentration (Cmax) [81 Days]

    maximum plasma concentration

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 55 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

  1. Are capable of giving informed consent and complying with study procedures;

  2. Are between the ages of 18 and 55 years, inclusive;

  3. Female subjects have a negative urine pregnancy test result at screening and Day 0, and meet one of the following criteria:

  4. Using a medically acceptable form of birth control for at least 1 month prior to screening (3 months on oral contraceptives) [e.g., hormonal contraceptives (oral, patch, injectable or vaginal ring), implantable device (implantable rod or intrauterine device), or a double barrier (e.g., diaphragm, cervical cap, oral, patch or vaginal hormonal contraceptive, condom, spermicide, or sponge)]

  5. Surgically sterile for at least 3 months prior to screening by one of the following means:

Bilateral tubal ligation Bilateral salpingectomy (with or without oophorectomy) Surgical hysterectomy Bilateral oophorectomy (with or without hysterectomy)

  1. Postmenopausal, defined as the following:

Last menstrual period greater than 12 months prior to screening Postmenopausal status confirmed by serum Follicle-Stimulating Hormone（FSH） and estradiol levels at screening;

  1. Considered healthy by the Investigator, based on subject's reported medical history, full physical examination, clinical laboratory tests, 12-lead ECG, and vital signs;

  2. Non-smoker and less than 5 cigarettes/day or nicotine replacement products in last 6 months;

  3. Body mass index (BMI) of 18.0 to 30.0 kg/m2 inclusive and body weight not less than 50 kg;

  4. Male subjects with female partners of child bearing potential must agree to use condoms for the duration of the study and until 12 weeks after dosing with the study drug and must refrain from donating sperm for this same period.

Exclusion Criteria:

  1. Subjects of non-Chinese nationality living or working in China, or persons of non-East Asian descent who are Chinese nationals;

  2. Clinically significant history of gastrointestinal, cardiovascular, musculoskeletal, endocrine, hematologic, psychiatric, renal, hepatic, bronchopulmonary, neurologic, immunologic, lipid metabolism disorders, or drug hypersensitivity as determined by the Investigator;

  3. History of food or drug allergy;

  4. Known or suspected malignancy;

  5. History of unexplained syncope, symptomatic hypotension or hypoglycemia;

  6. History or family history of long corrective QT interval（QTc） syndrome;

  7. History of chronic diarrhea, malabsorption, unexplained weight loss, food allergies or intolerance;

  8. Poor venous access;

  9. Positive blood screen for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), hepatitis C antibody or treponema pallidum antibody ;

  10. Donated or lost >500ml of blood in the previous 3 months;

  11. Taken an investigational drug or participated in a clinical trial within 3 months (or 5 half-lives), whichever is longer;

  12. Taken any prescription medications within 14 days or 5 half-lives (whichever is longer) of the first dose of study drug;

  13. Hospital admission or major surgery within 6 months prior to screening;

  14. A history of prescription drug abuse within 9 months prior to screening;

  15. A history of alcohol abuse according to medical history within 9 months prior to screening;

  16. Female subjects with positive pregnancy test, pregnant or breastfeeding;

  17. A positive screen for alcohol, drugs of abuse at screening;

  18. An unwillingness or inability to comply with food and beverage restrictions during study participation;

  19. Use of over-the-counter (OTC) medication and herbal within 7 days prior to dosing (Note: Use of acetaminophen at < 2 g/day is permitted until 24 hours prior to dosing);

  20. Any condition or finding that in the Investigators opinion would put the subject or study conduct at risk if the subject were to participate in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shanghai Xinhua Hospital Shanghai Shanghai China 200092

Sponsors and Collaborators

  • Youngene Therapeutics Inc., Ltd.

Investigators

  • Study Director: Jiaojuan He, Master, Youngene Therapeutics Inc., Ltd.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Youngene Therapeutics Inc., Ltd.
ClinicalTrials.gov Identifier:
NCT05089617
Other Study ID Numbers:
  • YG1699-102
First Posted:
Oct 22, 2021
Last Update Posted:
Jan 26, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Youngene Therapeutics Inc., Ltd.
Diabetes

Study Results

No Results Posted as of Jan 26, 2022