A Phase Ia Study of KMY Tablets in Healthy Subjects

NCT ID: NCT07314541

Last Updated: 2026-01-02

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-12-15
• Study Completion Date: 2026-11-07

Brief Summary

This is a Phase Ia, randomized, double-blind, placebo-controlled study conducted in healthy subjects. The study plans to enroll a total of 120 participants, with both males and females included in all parts.

The trial consists of three distinct parts:

Part A (Single-Ascending Dose, SAD): A total of 72 subjects will be enrolled to evaluate the safety, tolerability, and pharmacokinetics of single oral doses of KMY Tablets.

Part B (Multiple-Ascending Dose, MAD): A total of 36 subjects will be enrolled to evaluate the safety, tolerability, and pharmacokinetics of multiple oral doses of KMY Tablets.

Part C (Food-Effect): A total of 12 subjects will be enrolled to assess the impact of a high-fat, high-calorie meal on the pharmacokinetic profile of KMY Tablets.

The primary objectives are to evaluate the safety and tolerability of single and multiple doses of KMY Tablets and to assess the food effect on its pharmacokinetics. The secondary objectives include characterizing the single- and multiple-dose pharmacokinetics, investigating the drug's metabolism and excretion, and evaluating the safety and tolerability in the fed state. Exploratory pharmacodynamic parameters may also be investigated.

Detailed Description

This is a single-center, Phase Ia, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, and pharmacokinetics of KMY Tablets in healthy subjects. The study consists of three parts: a Single-Ascending Dose part, a Multiple-Ascending Dose part, and a Food-Effect part. A total of 120 subjects will be enrolled. The primary objectives are to assess the safety and tolerability profile and to investigate the effect of food on pharmacokinetics. Secondary objectives include characterizing the single- and multiple-dose pharmacokinetic profiles and investigating the metabolism and excretion of KMY Tablets

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

KMY Tablets

Participants will receive the active drug, KMY tablet. The study consists of three parts:

Part A (Single Ascending Dose): Participants will be assigned to one of eight predefined dose cohorts (2, 6, 10, 20, 40, 60, 90, or 120 mg) to receive a single dose of KMY tablet or matching placebo under fasting conditions.

Part B (Multiple Ascending Dose): Participants will be assigned to one of three predefined dose regimens (40 mg QD, 80 mg QD, or 40 mg BID) to receive KMY tablet or matching placebo for 7 consecutive days under fasting conditions.

Part C (Food Effect): All participants will receive a single dose of 60 mg KMY tablet in a two-period, two-sequence crossover design, once under fasting conditions and once after a high-fat, high-calorie meal.

This arm includes all participants who receive the active KMY tablet, regardless of the study part, dose level, or fed/fasting condition.

Group Type: EXPERIMENTAL

KMY Tablets

Intervention Type: DRUG

KMY Tablets is an investigational drug product. This study evaluates its safety, tolerability, and pharmacokinetics in healthy subjects.

KMY Tablets Placebo

Participants will receive a placebo tablet identical in appearance to the KMY tablet but containing no active ingredient. The placebo is used only in the randomized, double-blind, controlled portions of the study (Part A and Part B). Within each dose cohort of Part A and Part B, a subset of participants will be randomized to this arm.

This arm does NOT include participants from the open-label Part C study.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

A placebo tablet matching the appearance of the active KMY Tablets. It contains no active pharmaceutical ingredient.

Interventions

KMY Tablets

KMY Tablets is an investigational drug product. This study evaluates its safety, tolerability, and pharmacokinetics in healthy subjects.

Intervention Type: DRUG

Placebo

A placebo tablet matching the appearance of the active KMY Tablets. It contains no active pharmaceutical ingredient.

Intervention Type: DRUG

Other Intervention Names

Investigational Product; Placebo matching KMY Tablets

Eligibility Criteria

Inclusion Criteria

1. Healthy male or female participants aged 18 to 45 years (inclusive).

2. Male participants weigh ≥50.0 kg; female participants weigh ≥45.0 kg. Body Mass Index (BMI) is between 19.0 and 26.0 kg/m² (inclusive).

3. Participants agree to use effective contraception from screening until a specified period after the last dose and have no plan for pregnancy, sperm donation, or egg donation.

4. Voluntarily participate in the trial, fully understand the study, sign the informed consent form, and are able to comply with the study procedures.

Exclusion Criteria

1. Known history of allergy to the active ingredient, excipients of the investigational drug, or related compounds; or allergic constitution (e.g., allergy to two or more drugs or foods).

2. History or presence of severe chronic diseases of the cardiovascular, hepatic, renal, respiratory, hematological, endocrine, immune, psychiatric, or neurological systems within the past year, which in the investigator's judgment may compromise participant safety or study integrity.

3. Abnormal and clinically significant findings in vital signs, physical examination, laboratory tests (hematology, blood chemistry, urinalysis, coagulation), or 12-lead ECG at screening, as judged by the investigator.

4. Use of any medications (including prescription, over-the-counter, or herbal medicines) or health supplements within a specified period (e.g., 2 weeks) prior to screening.

5. Participation in another clinical trial (drug or medical device) or use of any other investigational drug within a specified period (e.g., 3 months) prior to screening.

6. History of drug abuse or positive urine drug screen.

7. Donation or loss of ≥400 mL of blood, or receipt of blood products, within a specified period (e.g., 6 months) prior to screening.

8. History of alcohol abuse, inability to abstain from alcohol during the study, or positive alcohol breath test.

9. Smoking more than a specified number of cigarettes per day (e.g., 5) within a specified period prior to screening, or inability to cease use of tobacco products during the study.

10. Intolerance to venipuncture or history of needle or blood phobia.

11. Any other condition that, in the investigator's opinion, may pose a risk to the participant or interfere with the evaluation of study results.

12. Pregnant or lactating women, or women with a positive pregnancy test.

13. Unwilling to use effective contraception during the study and for a specified period thereafter.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Lei Yunshang Group

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yanxia Yu, PhD

Role: PRINCIPAL_INVESTIGATOR

Suzhou Municipal Hospital

Locations

Suzhou Municipal Hospital

Suzhou, Jiangsu, China

Countries

China

Central Contacts

Yanfen Wang

Role: CONTACT

wangyanfen@lys.cn

+86-18662172332

Facility Contacts

Yanxia YU, PhD

Role: primary

yuyxsz@163.com

+86-150-5140-4960

Other Identifiers

2025-CP-KMY-01

Identifier Type: -

Identifier Source: org_study_id