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Life sciences · Phase 1 Trial
ClinicalTrials.gov · October 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07532655). This is a study registration, not published results. Lead sponsor: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.. Recruitment status: RECRUITING. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 60 participants (ESTIMATED). Conditions: Overweight or Obesity. Interventions: DRUG: SYH2082 Injection; DRUG: Placebo. Primary outcome measures: Number of Adverse Events as a measure of safety and tolerability of SYH2082 , SAD: Screening period up to day 57 MAD: Screening period up to day 85. Brief summary: To evaluate the safety and tolerability of single dose and multiple doses of SYH2082 Injection in healthy participants.