Study of SHR-1209 Administered by Single-site or Multiple-site Subcutaneous Injections in Healthy Volunteers

Phase 1

Not yet recruiting

• Conditions: Hypercholesterolemia and Hyperlipidemia
• Interventions: Drug: SHR-1209 single-site subcutaneous injection; Drug: SHR-1209 multiple-site subcutaneous injections

• Registration Number: NCT06837077
• Lead Sponsor: Jiangsu HengRui Medicine Co., Ltd.

Brief Summary

In order to improve the medication convenience and compliance of patients and facilitates in the long-term control of disease condition, it is planned to reduced the number of injections to one per administration. The study aims to compare the safety and pharmacokinetics data to assess feasibility of single-site and multiple-site injection for administration.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-01-07
• Status Verified: 2025-02
• Study Start: 2025-02
• Study First Submitted QC: 2025-02-18
• Last Update Submitted: 2025-02-18
• Study First Posted: 2025-02-20
• Last Update Posted: 2025-02-20
• Primary Completion: 2025-06
• Study Completion: 2025-07

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

1. Understanding the research procedures and methods, being able to complete the research in accordance with the procedure requirements, and sign the informed consent;
2. The age on the date of signing the informed consent must be ≥18 years old and ≤55 years old;
3. Body mass index (BMI) at screening period must be ≥19.0 kg/m2 and <28.0 kg/m2, weight of male must≥ 50.0 kg and <90.0 kg, and female≥ 45.0 kg and <90.0 kg;
4. The subjects and their female partners are willing to have no reproductive plan from signing the informed consent to 16 weeks after the last administration of the study drug, and voluntarily take effective contraceptive measures and do not plan to donate sperm or ovum.

Exclusion Criteria

1. Serious infection within 3 months before screening;
2. History of food or drug allergy or atopic allergic disease (asthma, urticaria);
3. Positive blood pregnancy test;
4. Have a history of drug abuse;
5. Women who are pregnant or breastfeeding;
6. Subjects who are considered by the investigator to have any other factors which are not suitable for participating in this study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Treatment group A	SHR-1209 single-site subcutaneous injection	-
Treatment group A	SHR-1209 multiple-site subcutaneous injections	-
Treatment group B	SHR-1209 single-site subcutaneous injection	-
Treatment group B	SHR-1209 multiple-site subcutaneous injections	-

Primary Outcome Measures

Name	Time	Method
Visual Analog Scale (VAS) was used to evaluate the injection site pain of single-site subcutaneous injection of SHR-1209.	After injection in day 1 and day 57.
Visual Analog Scale (VAS) was used to evaluate the injection site pain of multiple-site subcutaneous injections of SHR-1209.	After injections in day 1 and day 57.
Area under the curve (AUC0-56).	After injection in day 1 up to day 56.
Peak time (Tmax) of SHR-1209.	After injection in day 1 up to day 56.
Peak concentration (Cmax) of SHR-1209.	After injection in day 1 up to day 56.

Secondary Outcome Measures

Name	Time	Method
Subjects' preferred method of SHR-1209 administration between the tested injection regimens.	Day 68.
Incidence and severity of adverse events (AEs).	From Day 1 to Day 169.
Incidence and severity of serious adverse events (SAEs).	From Day 1 to Day 169.

Trial Locations

Locations (1)

The First Affiliated Hospital of USTC; 🇨🇳 Hefei, Anhui, China