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NCT06501586CompletedPhase 1

Study of SGB-3908 in Healthy Subjects and Mildly Hypertensive Subjects

A Phase 1, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Characteristics of SGB-3908 After a Single Administration in Healthy Subjects and Mildly Hypertensive Subjects

Source: ClinicalTrials.gov · Last updated 10 Feb 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic (PK), and pharmacodynamic (PD) effects of SGB-3908 in healthy subjects and mildly hypertensive subjects. The study will be a single ascending dose (SAD) phase.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
40 (actual)
First submitted
9 Jul 2024
Start date
31 Jul 2024
Primary completion date
7 Apr 2025
Lead sponsor
Suzhou Sanegene Bio Inc.
NCT number
NCT06501586

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 40
  • From 31 Jul 2024 to the primary completion date, 7 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has a history of hospitalization or other clinically significant diseases within 1 month before screening, major surgery within 6 months before screening, or other unstable conditions judged by the investigator;

Other illness

  • Has mental illness, liver and kidney disease, gastrointestinal disease, nervous system disease, or other related systemic diseases that affect the trial;
  • Has a history of orthostatic hypotension or syncope;

Lab values

  • Patients with clinically significant abnormalities confirmed by physical examination, 12-lead electrocardiogram, laboratory tests, etc., or those who meet any of the following conditions during screening need to be excluded:
    • Alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin higher than 1.5× upper limit of normal (ULN)
    • Serum creatinine (Cr) higher than ULN
    • Serum potassium higher than 5 mmol/L
    • QT/QTc interval prolongation during screening (QTcF\>450 ms)

Who the study is looking for

  • Has body mass index (BMI) ≥18 and ≤30 kg/m\^2 and has bodyweight ≥ 50 kg;
  • Has Systolic blood pressure (SBP) ≥100 mmHg and ≤150 mmHg and diastolic blood pressure (DBP) ≥65 mmHg and ≤95 mmHg at screening;

Age in the registry: 18 years to 55 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University Third Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.