Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study of SA030 Injection in Overweight or Obese Participants

This study is the first time SA030 is being given to people. The goal is to understand how safe it is, how well it is tolerated, and how the body processes and responds to a single dose of SA030 in individuals who are overweight or obese. Over the last few decades, more and more people around the world have become overweight or obese, and the numbers keep rising in almost every country. From 1990 to 2021, this problem grew steadily and reached its highest point in 2021.

Participants needed: 40
Trial details
Phase: Phase 1Age: 18-55Biological sex: AllType: InterventionalSponsor: Suzhou Siran Biotechnology Co.,Ltd.Updated: Mar 18, 2026Locations: 1
Eligibility criteria

You must be able to understand the study and sign a written consent form. [+5]

You cannot join if you have lost or gained more than 5 percent of your body weig... [+17]

Status: Recruiting

SA1211 Injection Phase 1 Study

The goal of this clinical trial is to evaluate the safety, tolerability, immunogenicity and Pharmacokinetics (PK) characteristics of SA1211 Injection in healthy volunteers (Part A) and participants with chronic hepatitis B (CHB, Part B), and assess its preliminary efficacy in participants with chronic hepatitis B (CHB). The main questions it aims to answer are: What are the safety, tolerability, immunogenicity and PK characteristics of a single subcutaneous injection of SA1211 Injection in healthy volunteers (Part A)? What are the safety, tolerability, immunogenicity and PK characteristics of multiple subcutaneous injections of SA1211 Injection in participants with CHB (Part B)? What is the preliminary efficacy of SA1211 Injection in participants with CHB (Part B)? Participants will: * Part A (healthy volunteers): Receive a single subcutaneous injection of SA1211 Injection or placebo and complete relevant safety, tolerability and PK monitoring as required. * Part B (participants with CHB): Receive multiple subcutaneous injections of SA1211 Injection or placebo and complete relevant safety, tolerability, PK monitoring and preliminary efficacy assessment as required.

Participants needed: 80
Trial details
Phase: Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: Suzhou Siran Biotechnology Co.,Ltd.Updated: Dec 10, 2025Locations: 1
Eligibility criteria

Able to correctly understand and sign the informed consent form in writing. [+9]

Participants with concurrent hepatitis C virus (HCV), human immunodeficiency vir... [+8]