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Completed

NCT Number: NCT04554043

The PK/PD Study of SHR7280 Tablets in Healthy Subjects.

The primary objective of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of SHR7280 tablets in healthy subjects.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Affiliated Hospital of Qingdao University

Qingdao, Shandong, 266000, China

About this study

GNRH antagonists can be used to treat sex hormone-dependent diseases, and SHR7280 is an oral GNRH antagonist. The purpose of this study is to observe the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple oral doses of SHR7280 in healthy subjects.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

PART 1:

  • Healthy males , aged 18-65;
  • BMI 18 ~ 30 kg/m2;
  • Subjects in general good health. No clinically significant findings in Physical examination and auxiliary examination.

PART 2:

  • premenopausal females, aged 18-45;
  • BMI 18 ~ 30 kg/m2;
  • Subjects in general good health. No clinically significant findings in Physical examination and auxiliary examination.

Exclusion criteria

PART 1

  • Testosterone (T) < 12 nmol/L;
  • ALT or AST or total bilirubin exceeds the upper limit of normal;
  • Those with positive nicotine test and alcohol breath test before administration, and those with positive drug screening before administration;
  • Use of any medication within 1 month before administration; or use of medication that does not exceed 5 half-lives, whichever is longer;
  • Subjects with chronic diseases or serious diseases that affect drug absorption, distribution, metabolism and excretion;
  • Blood donation or donation of blood components within 1 month before screening, or loss of blood equivalent to at least 200 mL, or transfusion within 2 months;
  • Use of GnRH agonists and GnRH antagonists within 6 months before screening and use of any androgens and antiandrogens within 5 half-lives before screening;
  • Subjects with severe infection, severe trauma or major surgery within 6 months before screening;
  • Positive results of infectious disease screening .
  • Allergic constitution or allergy to two or more kinds of food and drugs, including known history of allergy to the study drug or any component of the study drug.

PART 2:

  • Pregnant or breast feeding;
  • FSH≥25U/L;
  • Positive serum pregnancy test (serum β-HCG test) result;
  • Abnormal uterine bleeding within 3 months prior to screening
  • ALT or AST or total bilirubin exceeds the upper limit of normal;
  • Those with positive nicotine test and alcohol breath test before administration, and those with positive drug screening before administration;
  • Use of any medication within 1 month before administration; or use of medication that does not exceed 5 half-lives, whichever is longer;
  • Subjects with chronic diseases or serious diseases that affect drug absorption, distribution, metabolism and excretion;
  • Blood donation or donation of blood components within 1 month before screening, or loss of blood equivalent to at least 200 mL, or transfusion within 2 months;
  • GnRH agonist use 6 months prior to Screening and GnRH antagonist or any sex hormone use 2 months prior to Screening.
  • Subjects with severe infection, severe trauma or major surgery within 6 months before screening
  • Positive results of infectious disease screening .
  • Allergic constitution or allergy to two or more kinds of food and drugs, including known history of allergy to the study drug or any component of the study drug.

Treatment and study plan

SHR7280

Drug

treatment

Placebo oral tablet

Drug

blank control

Primary outcomes

  1. Number of Participants with Adverse events

    Time frame: Pre-dose to 28±2 days after dose administration

    Part 1 and Part 2

Secondary outcomes

  1. Area under the plasma concentration versus time curve (AUCτ) after the first dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit( 28±2 days after dose administration)

    Part 1 and Part 2

  2. Maximum observed serum concentration (Cmax) after the first dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  3. Time to maximum observed serum concentration (Tmax) after the first dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  4. Time to elimination half-life (T1/2) ;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  5. Apparent total clearance(CL/F) of the drug from plasma after last morning dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  6. Apparent volume of distribution(Vz/F) after last morning dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  7. Maximum observed serum concentration (Cmax) after last morning dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  8. Time to maximum observed serum concentration (Tmax) after last morning dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  9. Trough observed serum concentration (Ctrough) after last morning dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  10. Accumulation Factor(Racc)after last morning dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  11. Area under the plasma concentration versus time curve (AUCτ) after last morning dose of SHR7280;

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1 and Part 2

  12. Endocrine Parameters: Testosterone

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 1

  13. Endocrine Parameters: Estuarial

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 2

  14. Endocrine Parameters:Progesterone

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 2

  15. Endocrine Parameters: Luteinizing hormone

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 2

  16. Endocrine Parameters: Follicle stimulating hormone

    Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)

    Part 2

Sponsors and collaborators

Lead sponsor

Jiangsu HengRui Medicine Co., Ltd.

Industry

Registry information

Official study title

A Randomized, Double-blind, Dose-escalation, Placebo-controlled Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Oral Doses of SHR7280 Tablets in Healthy Subjects.

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Sep 18, 2020
Registry last updated
Oct 28, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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