A Study to Assess Safety and Tolerability of GS1-144 in Healthy Volunteers

NCT ID: NCT06204250

Last Updated: 2025-02-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 86 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-02-27
• Study Completion Date: 2024-12-19

Brief Summary

The primary purpose of this study is to assess the safety and tolerability of single ascending doses of GS1-144 in healthy participants in Part 1 and to assess the safety and tolerability of multiple ascending doses of GS1-144 in healthy postmenopausal female participants in Part 2.

Detailed Description

This study will be divided into two sequential parts: Part 1 single ascending dose (SAD), and Part 2 multiple ascending dose (MAD) with the overall design.

Part 1 will enroll a total of approximately 46 healthy participants in five cohorts at 5 milligram (mg), 15 mg, 30 mg, 60 mg and 90 mg dose levels. Each cohort will have 2 participants receiving placebo. There is no restriction on the male-to female ratio.

Part 2 will be conducted after confirming the safety and tolerability of the ->30mg dose in Part 1 and will enroll a total of approximately 30 healthy postmenopausal female participants and provisionally consists of three cohorts at 15 mg, 30 mg 60 mg and 120mg dose levels. Each cohort will have 2 participants receiving placebo.

Conditions

Vasomotor Symptoms; Adult Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: OTHER
• Blinding Strategy: DOUBLE

Study Groups

Part 1 Single Ascending Dose: Cohorts 1 to 6

Participants will receive GS1-144 5 mg, 15 mg, 30 mg, 60 mg , 90 mg and 120mg tablets once on Day 1 in their respective Cohort in Part 1. 2 participants will receive placebo in each cohort.

Group Type: EXPERIMENTAL

GS1-144

Intervention Type: DRUG

Oral tablets.

Placebo

Intervention Type: DRUG

Matching placebo tablets.

Part 2 Multiple Ascending Dose: Cohorts 1 to 4

tablets once on Day 1 in their respective Cohort in Part 2. 2 participants will receive placebo in each cohort.

Group Type: EXPERIMENTAL

GS1-144

Intervention Type: DRUG

Oral tablets.

Placebo

Intervention Type: DRUG

Matching placebo tablets.

Interventions

GS1-144

Oral tablets.

Intervention Type: DRUG

Placebo

Matching placebo tablets.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. At the time of signing the informed consent form (ICF): Part 1 only: healthy male and female participants aged between 18 and 45 years inclusive; Part 2 only: healthy women aged between 40 and 65 years inclusive who have undergone natural menopause;

2. Body weight >=50 kilogram (kg) (male), >=45 kg (female) with a body mass index between 18.0 and 32.0 kilogram per square meter (kg/m^2) inclusive at screening;

3. Part 1 only: Female participants are eligible to participate if they are not pregnant, not breastfeeding, and highly effective contraception includes placement of an intrauterine device or intrauterine system plus use of a condom;

4. Part 1 only: Male participants must agree to practice true abstinence; be surgically sterilized; or agree to use a condom plus effective contraception for their female partner, if of childbearing potential, from screening and for at least 90 days after dosing and refrain from donating sperm during this period. These contraception requirements do not apply if the male participant is in an exclusively same sex relationship;

5. Able to comprehend the nature of the study and any risks associated with participation and willing to cooperate and comply with protocol restrictions and requirements.

Exclusion Criteria

1. Any known allergy to the components or analogues of the investigational product, or those with an allergic constitution;

2. A history of currently suffering from any other cardiovascular, gastrointestinal, endocrine, hematological, hepatic, immunological, metabolic, urinary, pulmonary, neurological, dermatological, psychiatric, renal and/or other major diseases deemed clinically significant by the investigator;

3. Known/confirmed history of malignancy;

4. A history of epileptic seizure or increased risk of epileptic seizure, or participants with a recent history of head trauma leading to loss of consciousness or concussion;

5. A history of currently suffering from hypothalamic dysfunction;

6. Significant acute/chronic infections within two weeks prior to dosing;

7. Undergone major surgical procedures within six months prior to screening or plan to undergo any surgery during the trial;

8. Participated in other clinical trials within 1 month prior to dosing;

9. Have lost or donated more than 400 mL of blood within 1 month prior to screening;

10. Have taken any prescription/over-the-counter drugs or dietary supplements within 7 days prior to dosing or within 5 halflives of the drug;

11. Clinically significant abnormalities on physical examination or genitourinary ultrasound at the time of screening;

12. Clinically significant abnormalities in vital signs;

13. Prolonged QTcF interval in 12-lead ECG results ;

14. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), gamma-glutamyltransferase (GGT), total bilirubin (TBIL), blood creatinine (CRE), blood urea nitrogen (BUN), or international normalized ratio (INR) higher than the upper limit of normal (ULN) at screening, that are considered as clinically significant abnormalities by the investigator;

15. Part 2 only: abnormal sex hormone levels at screening that are considered clinically significant by the investigator;

16. Clinically significant abnormalities in thyroid function, parathyroid function, and neck ultrasound results at screening;

17. Women with positive pregnancy test result or those who are breastfeeding before dosing;

18. Positive hepatitis C virus antibody (HCV Ab), positive human immunodeficiency virus antibody (HIV Ab) or positive hepatitis B surface antigen (HbsAg) result at screening;

19. Unable to refrain from consuming grapefruit, pomelo, grapefruit juice, or pomelo juice from 48 hours prior to check-in until the end of the study;

20. Unable to refrain from consuming any foods or beverages containing caffeine or xanthine from 48 hours prior to check-in until the end of the study;

21. Unable to abstain from smoking/using tobacco products from 48 hours prior to check-in until the end of the study;

22. Unable to refrain from consuming alcohol from 48 hours prior to check-in until the end of the study;

23. Any history of narcotic use or drug abuse;

24. Any medical or other condition may affect the clinical trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Syneos Health

OTHER

Sponsor Role: collaborator

Changchun GeneScience Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Linear Clinical Research

Perth, Western Australia, Australia

Countries

Australia

Other Identifiers

GenSci074-102

Identifier Type: -

Identifier Source: org_study_id