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Completed

NCT Number: NCT03967548

The Germinal Peptide Eye Drops in Healthy Volunteers in a Clinical Study

The subjects of this study were healthy subjects, who were given medicine in a single dose group: 0.004%.

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Key information

Conditions

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Xiuli Zhao

Beijing, BJ10, China

About this study

Tear collection was conducted on the single dose D1 (that is, the day of administration). Collection points: 10 min, 30 min, 1 h, 2 h, 4 h, 6 h, 8 h, and 12 h after administration.Each time 5-50 mg (generally 20 mg), a total of 160-1600 mg of tears will be collected (during the screening period, all subjects will retain the tear samples collected by the Schirmer filter paper, among which, qualified tear samples will be used for blank samples or methodological investigation.After administration, only 1 tear collection site will be collected for each subject.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • healthy volunteers aged between 18 and 45, both male and female in each group;
  • body mass index between 19 and 26 kg/m2 (including critical value), male weight 50 kg, female weight 45 kg;
  • target eye Schirmer Ⅰ test (Schirmer filter paper bending, clip next eyelid medial 1/3 conjunctival sac within 5 min) tear wet filter paper length or greater 10 mm;
  • subjects will participate in the study voluntarily and sign the informed consent.

Exclusion criteria

  • binocular corrected vision < 1.0, abnormal intraocular pressure, slit lamp and fundus examination with clinical significance;
  • those with abnormal physical examination, vital signs, electrocardiogram and laboratory examination before the test with clinical significance;
  • patients with eye diseases, including history of inner eye surgery or laser surgery;
  • a medical history of central nervous system, spirit, cardiovascular system, kidney, liver, respiratory system, metabolism system and skeletal muscle system, which may endanger the safety of subjects or affect the results of the study;
  • positive test results of hepatitis b virus surface antigen (HBsAg), hepatitis c virus antibody (hcv-ab), treponema pallidum specific antibody (tp-ab) or human immunodeficiency virus antibody (hiv-p24 /Ab);
  • have a significant history of clinical allergy, especially drug allergy, especially allergic to any component of germinal peptide eye drops;
  • smoking more than 5 cigarettes per day on average;
  • those who are suspected or have alcohol dependence, and their alcohol intake is more than 2 units per day on average for 3 months (1 unit =10 mL ethanol, that is, 1 unit =200 mL beer with 5% alcohol or 25 mL spirit with 40% alcohol or 83 mL wine with 12% alcohol) or who have tested positive for alcohol;
  • history of drug abuse, or positive urine test of ketamine, morphine, methamphetamine, dimethylene dioxyamphetamine, tetrahydrocannabinic acid;
  • have taken any medicine within 2 weeks before screening;
  • participated in clinical trials within the first 3 months of screening;
  • blood donation or blood loss 400 mL within 3 months before screening;
  • have used ophthalmic drugs or eyelash growth solution in the first 2 weeks;
  • select the subjects who have worn contact lenses or contact lenses in the first 2 weeks;
  • pregnant or lactating women and those planning to become pregnant (including male subjects);No effective contraceptive measures were taken within 1 month prior to the inclusion of subjects, or subjects (including male subjects) were unwilling to take effective contraceptive measures within the next 6 months;
  • the researchers considered the participants unsuitable.

Treatment and study plan

Germinal peptide eye drops

Drug

Germinal peptide eye drops of 0.004%

Other names: shengfatai-eye drops

Primary outcomes

  1. Area under curve (0-t)

    Time frame: Within 12hours after administration

    AUC(0-t)

  2. Area under curve(0-∞)

    Time frame: Within 12hours after administration

    AUC(0-∞)

  3. Peak concentration

    Time frame: Within 12hours after administration

    Cmax

  4. Peak time

    Time frame: Within 12hours after administration

    Tmax

  5. Half life

    Time frame: Within 12hours after administration

    t1/2

  6. Apparent volume of distribution

    Time frame: Within 12hours after administration

    Vd

  7. Elimination rate constant

    Time frame: Within 12hours after administration

    Kel

  8. Mean residence time

    Time frame: Within 12hours after administration

    MRT

  9. Clearance

    Time frame: Within 12hours after administration

    CL or CL/F

Sponsors and collaborators

Lead sponsor

Zhaoke (Guangzhou) Ophthalmology Pharmaceutical Ltd.

Industry

Registry information

Official study title

To Evaluate the Local Pharmacokinetic Characteristics of Single Administration of Germinal Peptide Eye Drops in Healthy Volunteers in a Phase I Clinical Study

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
May 30, 2019
Registry last updated
Sep 17, 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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