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A Phase I Clinical Study on SHR6390 in Healthy Chinese Volunteers

Q

Qingdao University

Status and phase

Completed
Phase 1

Conditions

Healthy Volunteers

Treatments

Drug: SHR6390(150mg)
Drug: SHR6390(100mg)
Drug: SHR6390(125mg)

Study type

Interventional

Funder types

Other

Identifiers

NCT05354336
SHR6390-I-105

Details and patient eligibility

About

This study was to evaluate the pharmacokinetics and safety of SHR6390 at doses of 100 mg, 125 mg, and 150 mg after process modification in Chinese healthy volunteers. A single oral dose of SHR6390 was given to each group, including 100 mg, 125mg and 150mg of SHR6390.

Enrollment

36 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy Chinese male and female aged 18-45years with a minimum weight of 50 kg for male and 45 kg for female subjects and a body mass index (BMI) of 18-26 kg/m2 who provided written informed consent for participating in the study.
  • Without history of cardiovascular, hepatic, kidney, pulmonary, endocrine, gastrointestinal, neurological, or psychiatric disease.
  • No pregnancy plan during the trial or within 6 months after completion of the trial.
  • Voluntarily signed the informed consent form and strictly adherence to the study protocol.

Exclusion criteria

  • vital signs, physical examination, 12-lead electrocardiogram, and laboratory examination had results of clinical significance.
  • Hepatitis B and C, human immunodeficiency virus (HIV) and syphilis antibody positive;
  • Any history of allergy, alcohol and drug abuse;
  • blood donation, massive blood loss (≥400mL).
  • Participated in other clinical trials within three months. (6) Severe infection or surgery four weeks prior to screening;
  • use of any drug that inhibits or induces hepatic metabolizing enzymes four weeks prior to screening;
  • use of any prescription drugs, over-the-counter drugs, Chinese herbal medicines and health care products fourteen days prior to screening;
  • A history of dysphagia, gastrointestinal ulcers, or any gastrointestinal disease that interferes with drug absorption.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 3 patient groups

SHR6390(100mg)
Experimental group
Treatment:
Drug: SHR6390(100mg)
SHR6390(125mg)
Experimental group
Treatment:
Drug: SHR6390(125mg)
SHR6390(150mg)
Experimental group
Treatment:
Drug: SHR6390(150mg)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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