A Drug-drug Interaction Study of SHR2150 on Healthy Chinese Volunteers

NCT05141422 | Unknown Phase 1

• 1 other identifier: SHR2150-I-105
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

The study is a single-centre, open-label, fixed-sequence, self-controlled clinical trial. It is planned to enroll 20 healthy adult subjects. Subjects will take SHR2150 on Day 1 and Day 21, and take efavirenz from Day 7 to Day 26.

Conditions

Human Immunodeficiency Virus Infection

Outcome Measures

Primary Outcomes (5)

• Tmax

  Time to maximum observed serum concentration (Tmax) for SHR2150 after Single dose

  from Day 1 to Day 7 after the first dose and from Day 21 to Day 27 after the second dose

• Cmax

  Maximum observed serum concentration (Cmax) for SHR2150 after Single dose

  from Day 1 to Day 7 after the first dose and from Day 21 to Day 27 after the second dose

• AUC0-t

  Area under the plasma concentration versus time curve (AUC0-t) for SHR2150 after Single dose

  from Day 1 to Day 7 after the first dose and from Day 21 to Day 27 after the second dose

• AUC0-inf

  Area under the plasma concentration versus time curve (AUC0-inf ) for SHR2150 after Single dose

  from Day 1 to Day 7 after the first dose and from Day 21 to Day 27 after the second dose

• T1/2

  Time to elimination half-life (T1/2) for for SHR2150 after Single dose

  from Day 1 to Day 7 after the first dose and from Day 21 to Day 27 after the second dose

Secondary Outcomes (1)

• Number of subjects with adverse events and the severity of adverse events

  from Day 1 to Day 37 after the first dose

Study Arms (1)

Treatment group

EXPERIMENTAL

SHR2150+ efavirenz

Drug: SHR2150 tablet、efavirenz

Interventions

SHR2150 tablet、efavirenz DRUG

SHR2150 tablet single dose, Efavirenz single dose.

Treatment group

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• The subject can communicate well with the researcher, understand and comply with the requirements of this study, and understand and sign the informed consent;
• Healthy subjects aged 18 \~ 45 (including the boundary value), male and female;
• Male body weight ≥ 50 kg, female body weight ≥ 45 kg, body mass index (BMI) within the range of 18 \~ 26 kg/m2 (including the boundary value) (BMI= weight (kg)/height 2 (m2));
• The physical examination, vital signs, laboratory examination, 12-lead electrocardiogram, abdominal B-ultrasound, and chest radiograph are normal or have no clinical significance;
• The subjects with reproduction ability must agree to take effective contraceptive measures after signing the informed consent form and within 7 months (for female) or 4 months (for male) until the last medication.

You may not qualify if:

• Anyone who has suffered from any clinical serious disease such as the circulatory system, endocrine system, nervous system, digestive system, respiratory system, urogenital system, hematology, immunology, psychiatry and metabolic abnormalities, or any other disease which can affect the study results;
• Those who have undergone surgery within 3 months before the trial, or plan to perform surgery during the study period;
• Those whose 12-lead ECG is abnormal with clinically significant or ECG QT interval (QTcF) ≥ 450 ms (for male) or \> 460 ms (for female) or \< 300 ms;
• Those who donated blood or suffered heavy blood loss (≥400 mL), received blood transfusions, or used blood products within 3 months before enrollment;
• Have a history of allergies to drugs, food or other substances;
• Those who have used soft drugs or hard drugs; or those with positive results in urine drug abuse screening;
• Those who have participated in any clinical trials and have taken study drugs within 3 months before the first administration;
• Those who have taken any medicine within 1 month before the first administration (including prescription medicines, non-prescription medicines, Chinese herbal medicines, vitamins, calcium tablets and other food supplements), especially the drugs which have any effect on CYP3A4;
• Regular drinkers within 3 months before the test, that is, drinking more than 15 g of alcohol per day (15 g alcohol = 450 mL of beer, or 50 mL of spirits, or 150 mL of wine), and any alcohol-containing products cannot be stopped during the study;
• Hepatitis B virus surface antigen is positive, or hepatitis C virus antibody is positive, or treponema pallidum antibody is positive, or human immunodeficiency virus antibody is positive;
• Women with pregnancy or within lactation period.

Sponsors & Collaborators

• Jiangsu HengRui Medicine Co., Ltd.: lead

Study Sites (1)

The People's Hospital of Liaoning Province

Shenyang, Liaoning, 110067, China

Location

MeSH Terms

Conditions

Acquired Immunodeficiency Syndrome

Condition Hierarchy (Ancestors)

HIV Infections; Blood-Borne Infections; Communicable Diseases; Infections; Sexually Transmitted Diseases, Viral; Sexually Transmitted Diseases; Lentivirus Infections; Retroviridae Infections; RNA Virus Infections; Virus Diseases; Slow Virus Diseases; Genital Diseases; Urogenital Diseases; Immunologic Deficiency Syndromes; Immune System Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: BASIC SCIENCE
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: The study is a single-centre, single-arm, open-label and fixed-sequence clinical trial.

Study Record Dates

• First Submitted: November 19, 2021
• First Posted: December 2, 2021
• Study Start: December 13, 2021
• Primary Completion: January 15, 2022
• Study Completion: January 22, 2022
• Last Updated: December 20, 2021

Record last verified: 2021-12

Locations

CN (1)