The Relative Bioavailability of INS068 Injection With Two Different Formulations in Healthy Subjects

Study on Bioavailability Study of INS068 Injection by Subcutaneous Injection of New and Old Formulations in Healthy Subjects

The study is a single-centre, randomized, open, 2-period, 2-sequence crossover design clinical trial. It is planned to enroll 24 healthy male subjects. Subjects will receive INS068 injection on Day1 and Day8.

Study Overview

• Status: Completed
• Conditions: Diabetes Mellitus
• Intervention / Treatment: Drug: INS068 injection; Drug: INS068 injection

• Study Type: Interventional
• Enrollment (Actual): 24
• Phase: Phase 1

Contacts and Locations

Study Locations

• China
  • Shandong
    • Jinan, Shandong, China, 150036
      • The Qian Foshan Hospital of Shandong Province

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 55 years (Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

1. The subject can communicate well with the researcher, understand and comply with the requirements of this study, and understand and sign the informed consent.
2. Healthy subjects aged 18 ~ 55 (including the boundary value), healthy male.
3. Body mass index (BMI) within the range of 18 ~ 27 kg/m2 (including the boundary value) (BMI= weight (kg)/height 2 (m2)).
4. The physical examination, vital signs, laboratory examination, 12-lead electrocardiogram, abdominal B-ultrasound, and chest radiograph are normal or have no clinical significance.

Exclusion Criteria:

1. Presence of any abnormal and clinically significant laboratory tests (blood routine, blood biochemistry, urine routine, coagulation function), Hemoglobin < 120g/L; White blood cells < 3.0 ×109/L; Platelets < 100 × 109/L;Serum creatinine > upper limit of normal (ULN);Transaminases (ALT, AST) > 2 times the upper limit of normal (2 × ULN);Alkaline phosphatase > 2 times the upper limit of normal (2 × ULN); Total bilirubin > 1.5 times the upper limit of normal (1.5× ULN) ;Fasting blood glucose >6.1mmol/L or <3.9mmol/L; HbA1c≥6.5%.

2、12-lead electrocardiogram (ECG) showed abnormal and clinically significant. 3、Hepatitis B surface antigen positive, hepatitis C antibody positive. 4、Positive human immunodeficiency virus (HIV) serology and positive syphilis serology.

5、Have a history of hypertension, or have a systolic blood pressure of 90-139 mmHg or a diastolic blood pressure outside the range of 60-89 mmHg at screening.

6、Life-threatening disease (cancer other than basal cell skin cancer or squamous cell skin cancer) within 5 years.

7、Severe infectious disease of vital organs within 1 month before screening. 8、History of serious cardiovascular disease, including decompensated heart failure (NYHA class III and IV), unstable angina, stroke or transient ischemic attack, myocardial infarction, persistent and clinically significant rhythm Abnormal, or have undergone coronary artery bypass grafting or percutaneous coronary intervention, etc..

9、Use of prescription drugs (topical eye/nasal drops and creams and occasional antipyretic and analgesic drugs such as acetaminophen within recommended doses are permitted) and over-the-counter drugs, dietary supplements, vitamins, and Chinese herbal medicine (regular vitamins are allowed).

10、A history of recurrent or severe drug food allergy, or known or suspected allergy to any component of the study drug.

11、Those who have participated in any drug clinical trials within 3 months before screening, who participated in clinical trials are defined as: those who have used test drugs; The elder shall prevail).

12、Alcoholism within 3 months prior to screening (average ≥14 units of alcohol per week: 1 unit = 285 mL of beer, or 25 mL of spirits, or 100 mL of wine); alcohol or alcohol consumption within 48 hours prior to dosing Gas test result is positive.

13、Smokers (at least 5 cigarettes per day in the 1 year prior to screening) or non-smokers (less than 5 cigarettes per day in the 1 year prior to screening) who smoked (including nicotine replacement use) within 48 hours prior to dosing; during the trial Inability or unwillingness to smoke, nicotine gum, or transdermal nicotine patches.

14、Drinking/eating coffee, tea, chocolate or soft drinks such as cola containing methylxanthines (theophylline, caffeine or theobromine) long-term or within 48 hours before administration.

15、Do vigorous exercise, such as weightlifting, sprinting, long-distance running, cycling, swimming, football, etc., within 48 hours before administration.

16、Known or suspected history of drug abuse or positive urine drug screening test within 5 years prior to screening.

17、Donate blood within 1 month before screening; or donate blood ≥ 400 mL within 3 months before screening, or have trauma or major surgical operation with blood loss ≥ 400 mL.

18、Mentally incapacitated or language-impaired subjects who cannot adequately understand or participate in the trial process.

19、The investigator evaluates that the subject has poor compliance or the condition of the vein in the arm cannot draw blood, or has a history of fainting blood and needles.

20、Males of childbearing potential but unwilling to use contraception during the trial and for four weeks after administration.

21、At the discretion of the investigator, there are any other circumstances that interfere with the conduct of the trial or the assessment of the results.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Treatment group A; T - R(T: new formulation, R: old formulation)	Drug: INS068 injection; Group A subjects were injected formulation T and formulation R of INS068 injection at Day1 and Day8.; Drug: INS068 injection; Group B subjects were injected formulation R and formulation T of INS068 injection at Day1 and Day8.
Experimental: Treatment group B; R -T(T: new formulation, R: old formulation)	Drug: INS068 injection; Group A subjects were injected formulation T and formulation R of INS068 injection at Day1 and Day8.; Drug: INS068 injection; Group B subjects were injected formulation R and formulation T of INS068 injection at Day1 and Day8.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Maximum observed serum concentration (Cmax) of INS068 injection	from Day1 to Day5 after the first cycle（each cycle is 5 days） and from Day8 to Day12 after the second cycle（each cycle is 5 days）
Area under the plasma concentration versus time curve (AUC0-t) of INS068 injection	from Day1 to Day5 after the first cycle（each cycle is 5 days） and from Day8 to Day12 after the second cycle（each cycle is 5 days）
Area under the plasma concentration versus time curve (AUC0-inf ) of INS068 injection	from Day1 to Day5 after the first cycle（each cycle is 5 days） and from Day8 to Day12 after the second cycle（each cycle is 5 days）

Secondary Outcome Measures

Outcome Measure	Time Frame
Time to maximum observed serum concentration (Tmax) of INS068 injection	from Day1 to Day5 after the first cycle（each cycle is 5 days） and from Day8 to Day12 after the second cycle（each cycle is 5 days）
Time to elimination half-life (T1/2) of INS068 injection	from Day1 to Day5 after the first cycle（each cycle is 5 days） and from Day8 to Day12 after the second cycle（each cycle is 5 days）
The Clearance (CL/F) of INS068 injection	from Day1 to Day5 after the first cycle（each cycle is 5 days） and from Day8 to Day12 after the second cycle（each cycle is 5 days）
The apparent volume of distribution (Vz/F) of INS068 injection	from Day1 to Day5 after the first cycle（each cycle is 5 days） and from Day8 to Day12 after the second cycle（each cycle is 5 days）
Number of subjects with adverse events and the severity of adverse events	from Day1 to Day16 after the first dose

Collaborators and Investigators

• Sponsor: Jiangsu HengRui Medicine Co., Ltd.

Study record dates

Study Major Dates

• Study Start (Actual): May 12, 2022
• Primary Completion (Actual): May 26, 2022
• Study Completion (Actual): June 2, 2022

Study Registration Dates

• First Submitted: April 8, 2022
• First Submitted That Met QC Criteria: April 19, 2022
• First Posted (Actual): April 20, 2022

Study Record Updates

• Last Update Posted (Actual): June 8, 2023
• Last Update Submitted That Met QC Criteria: June 6, 2023
• Last Verified: June 1, 2023

More Information

Terms related to this study

• Other Study ID Numbers: INS068-104

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No