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The Phase I Study of Recombinant Human Nerve Growth Factor Injection

Primary Purpose

Injury of Optic Nerve

Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Recombinant human nerve growth factor injection,experimental
Recombinant human nerve growth factor injection,single dose
Recombinant human nerve growth factor injection,multiple dose
Sponsored by
Beijing Tongren Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Injury of Optic Nerve

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

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.

Sites / Locations

  • Beijing Tongren HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm 9

Arm 10

Arm Type

Experimental

Experimental

Placebo Comparator

Placebo Comparator

Placebo Comparator

Placebo Comparator

Placebo Comparator

Placebo Comparator

Placebo Comparator

Placebo Comparator

Arm Label

3.75μg (pre test)

7.5μg

15μg single dose

30μg single dose

45μg single dose

60μg single dose

75μg single dose

90μg single dose

30μg multiple dose

45μg multiple dose

Arm Description

Single dose

Single dose

Intramuscular injection once

Intramuscular injection once

Intramuscular injection once

Intramuscular injection

Intramuscular injection

Intramuscular injection once

The dosage will be adjusted according to the actual situation of the trial

The dosage will be adjusted according to the actual situation of the trial

Outcomes

Primary Outcome Measures

Incidence of adverse events
Record the number of participants with abnormal laboratory values and/or adverse events,calculate frequency and percentage based on correlation with the investigational drug.
Area under curve (AUC) after injection of single dose/multiple dose
To measure the drug concentration in blood samples which collected after injection
Cmax after injection of single dose/multiple dose
To measure the drug concentration in blood samples which collected after injection
Tmax after injection of single dose/multiple dose
To measure the drug concentration in blood samples which collected after injection
T1/2 after injection of single dose/multiple dose
To measure the drug concentration in blood samples which collected after injection

Secondary Outcome Measures

Percentage of Participants With anti-drug antibodies
Percentage of participants with treatment-emergent positive anti-drug antibodies was summarized by treatment group.

Full Information

First Posted
January 12, 2020
Last Updated
August 10, 2021
Sponsor
Beijing Tongren Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04232332
Brief Title
The Phase I Study of Recombinant Human Nerve Growth Factor Injection
Official Title
The Phase I Study of Recombinant Human Nerve Growth Factor Injection in Healthy Chinese Volunteers on Safety, Tolerability and Pharmacokinetics: Randomized, Double-blind, Placebo-controlled, Single / Multiple Dose
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 26, 2019 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
March 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Beijing Tongren Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief 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
Detailed Description
This is a randomized, double-blind, placebo-controlled, single / multiple dose trial. recombinant human nerve growth factor injection in healthy Chinese volunteers on safety, and pharmacokinetics.The volunteers will be given the drug by intramuscular injection. The main purpose of this trial is to investigate the safety, tolerability , pharmacokinetics and immunogenicity of Chinese healthy volunteers after intramuscular injection of recombinant human nerve growth factor injection, to provide a safe dose range for subsequent clinical trials, as well as a safe and reasonable drug delivery program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Injury of Optic Nerve

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Sequential Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
86 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
3.75μg (pre test)
Arm Type
Experimental
Arm Description
Single dose
Arm Title
7.5μg
Arm Type
Experimental
Arm Description
Single dose
Arm Title
15μg single dose
Arm Type
Placebo Comparator
Arm Description
Intramuscular injection once
Arm Title
30μg single dose
Arm Type
Placebo Comparator
Arm Description
Intramuscular injection once
Arm Title
45μg single dose
Arm Type
Placebo Comparator
Arm Description
Intramuscular injection once
Arm Title
60μg single dose
Arm Type
Placebo Comparator
Arm Description
Intramuscular injection
Arm Title
75μg single dose
Arm Type
Placebo Comparator
Arm Description
Intramuscular injection
Arm Title
90μg single dose
Arm Type
Placebo Comparator
Arm Description
Intramuscular injection once
Arm Title
30μg multiple dose
Arm Type
Placebo Comparator
Arm Description
The dosage will be adjusted according to the actual situation of the trial
Arm Title
45μg multiple dose
Arm Type
Placebo Comparator
Arm Description
The dosage will be adjusted according to the actual situation of the trial
Intervention Type
Drug
Intervention Name(s)
Recombinant human nerve growth factor injection,experimental
Other Intervention Name(s)
Experimental
Intervention Description
Intramuscular injection once on the first day according to dose requirements
Intervention Type
Drug
Intervention Name(s)
Recombinant human nerve growth factor injection,single dose
Other Intervention Name(s)
Placebo
Intervention Description
Intramuscular injection once on the first day according to dose requirements
Intervention Type
Drug
Intervention Name(s)
Recombinant human nerve growth factor injection,multiple dose
Other Intervention Name(s)
Placebo
Intervention Description
Intramuscular injection once daily for 7 days according to dose requirements
Primary Outcome Measure Information:
Title
Incidence of adverse events
Description
Record the number of participants with abnormal laboratory values and/or adverse events,calculate frequency and percentage based on correlation with the investigational drug.
Time Frame
Single dose: 28 days / Multiple dose: 34 days
Title
Area under curve (AUC) after injection of single dose/multiple dose
Description
To measure the drug concentration in blood samples which collected after injection
Time Frame
Single dose: 24 hours / Multiple doses: 8 days
Title
Cmax after injection of single dose/multiple dose
Description
To measure the drug concentration in blood samples which collected after injection
Time Frame
Single dose: 24 hours / Multiple doses: 8 days
Title
Tmax after injection of single dose/multiple dose
Description
To measure the drug concentration in blood samples which collected after injection
Time Frame
Single dose: 24 hours / Multiple doses: 8 days
Title
T1/2 after injection of single dose/multiple dose
Description
To measure the drug concentration in blood samples which collected after injection
Time Frame
Single dose: 24 hours / Multiple doses: 8 days
Secondary Outcome Measure Information:
Title
Percentage of Participants With anti-drug antibodies
Description
Percentage of participants with treatment-emergent positive anti-drug antibodies was summarized by treatment group.
Time Frame
Single dose: 28 days / Multiple dose: 34 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age: 18-45 years old, including boundary value; 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); volunteers participated in the study voluntarily and signed informed consent. Exclusion Criteria: Take any prescription or over-the-counter drugs within 2 weeks before screening; Those who have been vaccinated within 3 months before screening; Those who participated in any clinical trial within 3 months before screening; 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; Diseases with clinical significance within 2 weeks before screening; Those who had major surgery, trauma or hospitalization within 6 months before screening; There is tattoo or other influence on the injection site to observe the skin condition; 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; There is a significant history of allergy in clinic, especially the history of drug allergy, especially the allergy to any component of zx1305 injection; 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; 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; Those who smoked more than 5 cigarettes per day in the first half year of screening; 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; 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; The condition of peripheral venous access is poor (difficult to collect blood); There are other reasons that the researchers think should not be selected.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Feng Wu
Phone
010-58268422
Email
bjtrec@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yi Zhang
Phone
025-58310595
Email
Zhang.Yi@xintrum.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiuli Zhao
Organizational Affiliation
Beijing Tongren Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Tongren Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Feng Wu
Phone
010-58268422
Email
bjtrec@126.com
First Name & Middle Initial & Last Name & Degree
Xiuli Zhao

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Phase I Study of Recombinant Human Nerve Growth Factor Injection

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