Overview

The Phase I Study of Recombinant Human Nerve Growth Factor Injection

Status:
Recruiting
Trial end date:
2022-03-31
Target enrollment:
0
Participant gender:
All
Summary
A randomized, double-blind, placebo-controlled, single/multiple dose study of recombinant human nerve growth factor injection in healthy Chinese volunteers on safety, tolerability and pharmacokinetics
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Beijing Tongren Hospital
Treatments:
Mitogens
Criteria
Inclusion Criteria:

1. Age: 18-45 years old, including boundary value;

2. The body weight meets the standard, the body weight of male volunteers is not less
than 50kg, the body weight of female volunteers is not less than 45kg, the body mass
index is in the range of 19-24kg / m2, the body mass index = body weight (kg) / height
(M2);

3. volunteers participated in the study voluntarily and signed informed consent.

Exclusion Criteria:

1. Take any prescription or over-the-counter drugs within 2 weeks before screening;

2. Those who have been vaccinated within 3 months before screening;

3. Those who participated in any clinical trial within 3 months before screening;

4. Those who lost blood or donated more than 200 ml blood within 4 weeks before screening
or who intend to donate blood during the study or within 4 weeks after the end of the
study;

5. Diseases with clinical significance within 2 weeks before screening;

6. Those who had major surgery, trauma or hospitalization within 6 months before
screening;

7. There is tattoo or other influence on the injection site to observe the skin
condition;

8. Patients with history of central nervous system, mental system, cardiovascular system,
urinary system, digestive system, respiratory system, metabolism system, blood system,
immune system, endocrine system and skeletal muscle system may endanger the safety of
the subjects or affect the research results according to the judgment of the
researchers;

9. There is a significant history of allergy in clinic, especially the history of drug
allergy, especially the allergy to any component of zx1305 injection;

10. The five items of hepatitis B (hepatitis B surface antigen, hepatitis B surface
antibody, hepatitis B e antigen, hepatitis B e antibody, hepatitis B core antibody),
hepatitis C antibody, syphilis specific antibody or AIDS joint test have clinical
significance;

11. It is suspected that there is alcohol dependence, and the average alcohol intake in
the first half year of screening is more than 2 units per day (1 unit = 10ml alcohol,
i.e. 1 unit = 200ml beer with 5% alcohol or 25ml spirits with 40% alcohol or 83ml wine
with 12% alcohol) or the alcohol test is positive;

12. Those who smoked more than 5 cigarettes per day in the first half year of screening;

13. Those who had a history of drug abuse or had taken drugs within one year before
screening, or who were positive in urine test of ketamine, morphine, methamphetamine,
dimethyldioxygoamphetamine and tetrahydrocannabinolic acid;

14. Women who are positive in pregnancy, lactation, blood pregnancy or who have not taken
effective contraceptive measures in the last month, and men or women who are not
willing to take effective non drug contraceptive measures during the whole trial
period and who are not willing to take effective contraceptive measures within one
year after the end of the trial;

15. The condition of peripheral venous access is poor (difficult to collect blood);

16. There are other reasons that the researchers think should not be selected.