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Search / Trial NCT05505955

Study of HRS-5965 in Healthy Subjects and Subjects With Renal Insufficiency

Launched by CHENGDU SUNCADIA MEDICINE CO., LTD. · Aug 16, 2022

Trial Information

Current as of July 22, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • - Healthy subjects study
  • 1. Healthy male or female, age ≥ 18 years old and ≤ 70 years old (on the day of signing the informed consent);
  • 2. 18.5kg/m2 ≤BMI\<30 kg/m2, and the weight of men should be ≥ 50kg, and that of women should be ≥ 45kg.
  • Study on subjects with renal insufficiency
  • 1. Age ≥ 18 years old and ≤ 70 years old (on the day of signing the informed consent), both men and women can;
  • 2. 18.5kg/m2≤BMI\<30 kg/m2;
  • 3. The estimated glomerular filtration rate of subjects with chronic renal insufficiency conforms to 15 ≤ EGFR \< 30 ml/min/1.73m2 (calculated according to CKD-EPI formula, see Appendix 2 of the scheme).
  • Exclusion Criteria:
  • - Healthy subjects study
  • 1. The researcher has determined that there may be diseases or medical conditions that affect the absorption, distribution, metabolism and excretion of drugs or reduce compliance;
  • 2. The estimated glomerular filtration rate conforms to EGFR \< 90 ml/min/1.73m2 (calculated according to CKD-EPI formula, see Appendix 2 of the scheme);
  • 3. According to the judgment of the researcher, any physiological or psychological disease or condition that may increase the risk of the test, affect the subject's compliance with the protocol, or affect the subject's completion of the test.
  • Study on subjects with renal insufficiency
  • 1. Those who received renal replacement therapy within 12 weeks before screening; Or the two tests in the screening period indicate that the renal function is unstable (the results in the screening period meet the diagnostic criteria of 2012 KDIGO acute renal injury, or the changes that do not meet the above criteria but are judged to be clinically significant by the researcher. If there are reasonable reasons, the third test is allowed, and the interval between two consecutive tests should be more than 3 days but not more than 7 days);
  • 2. According to the judgment of the researcher, the subject has any of the following: in the state of progression or prognosis of disease (including primary renal disease, complications and other complications); The treatment plan needs to be adjusted at any time; Any physical or mental disease or condition that may increase the risk of the test, affect the subject's compliance with the protocol, or affect the subject's completion of the test.

About Chengdu Suncadia Medicine Co., Ltd.

Chengdu Suncadia Medicine Co., Ltd. is a leading biotechnology firm based in Chengdu, China, specializing in the research and development of innovative therapeutic solutions. With a strong focus on advancing healthcare through cutting-edge clinical trials, the company is dedicated to improving patient outcomes across various therapeutic areas. Leveraging a team of experienced professionals and state-of-the-art technology, Chengdu Suncadia Medicine Co., Ltd. is committed to fostering the development of safe and effective medications, ensuring compliance with international regulatory standards, and contributing to the global medical community.

Locations

Qingdao, Shandong, China

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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