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NCT07117474CompletedPhase 1

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of a Single Subcutaneous Injection of HRS-9563 in Subjects With Mild Hypertension: a Randomized, Double-blind, Placebo-controlled Phase I Study.

Source: ClinicalTrials.gov · Last updated 24 Aug 2026

Brief summary (registry, in English)

To evaluate the safety and tolerability of a single subcutaneous injection of HRS-9563 in hypertensive subjects

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
60 (actual)
First submitted
9 Jul 2025
Start date
24 Dec 2024
Primary completion date
9 Jun 2026
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
NCT number
NCT07117474

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 60
  • From 24 Dec 2024 to the primary completion date, 9 Jun 2026
  • 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

  • Recently received any antihypertensive medications or medications that affect blood pressure.

Other illness

  • Secondary hypertension;

Lab values

  • History of type 2 diabetes mellitus or poorly controlled blood glucose;

Other

  • Abnormal daily life rhythm;
  • Any blood biochemical indicator during screening or baseline did not meet the standards in the exclusion criteria;
  • Mean sitting diastolic blood pressure ≥ 100 mmHg;
  • Orthostatic hypotension;

Who the study is looking for

  • Males or infertile women aged 18-65 years (inclusive);
  • Body mass index in the range of 19-28 kg/m2 (inclusive);
  • Mild primary hypertension, without antihypertensive treatment, with a mean sitting systolic blood pressure ≥ 130 mmHg and ≤ 159 mmHg during screening and baseline, and a mean 24-hour ambulatory systolic blood pressure ≥ 130 mmHg during screening.

Age in the registry: 18 years to 65 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
Zhejiang Provincial People's Hospital
Coordinator of this site? Confirm its status
HangzhouChinaUnknown status

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