← Eichor
Study identifier: NCT07254481 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

VB19055 Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study in a Healthy Chinese Population

Condition: Hypertension  ·  Sponsor: Zhejiang Yangli Pharmaceutical Technology Co., Ltd.

PhasePhase 1
Planned participants86
Who can joinAll sexes, 18 Years to 50 Years
Healthy volunteersYes

About this study

The purpose of this study is to evaluate the safety,tolerability,pharmacokinetics and pharmacodynamics of VB19055 in the healthy Chinese population.

This description comes directly from the study's public registry record.

Talk to the study team

Jia Song  ·  China 86+18503817651  ·  songjia@vybio.com

Xiaoqi Cao  ·  China 86+15238088632  ·  caoxiaoqi@vybio.com

Always discuss trial participation with your own doctor first.

Locations (2)

Hangzhou First People's HospitalHangzhou, ChinaRecruiting
Ruijin Hospital Affiliated to Shanghai Jiaotong University School of MedicineShanghai, ChinaNot Yet Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07254481