A Phase I Clinical Trial of Bevacizumab Injection

Lung Cancer Clinical Trial

Official title:

A Randomized, Double-blind, Single Dose, Parallel Comparison of Bevacizumab Injection and Avastin ® Phase I Clinical Study on the Similarity of Pharmacokinetics and Safety of Traditional Chinese Medicine in Healthy Male Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05476341
• Other study ID #: ZDTQ-2017-BFZDK
• Status: Completed
• Phase: Phase 1
• Start date: April 6, 2017
• Est. completion date: August 18, 2017

Study information

• Verified date: July 2022
• Source: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Recombinant humanized monoclonal antibody injection against human vascular endothelial growth factor (bevacizumab) is Avastin produced by Zhengda Tianqing Pharmaceutical Group Co., Ltd Biological similar drugs. Its mechanism is to prevent VEGF from binding to its natural receptor VEGFR, inhibit the proliferation and activation of vascular endothelial cells, and play an anti angiogenesis and anti-tumor role by binding with VEGF. A randomized, double-blind, single dose, parallel comparison of bevacizumab injection and Avastin is planned The phase I clinical study on the similarity of pharmacokinetics and safety of traditional Chinese medicine in healthy male volunteers aims to compare bevacizumab injection with Avastin The similarity of pharmacokinetics, tolerance, safety and immunogenicity.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 98
• Est. completion date: August 18, 2017
• Est. primary completion date: August 18, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• 1 Fully understand the purpose of the test, and basically understand the pharmacological effects and possible adverse reactions of the research drugs; Voluntarily sign written informed consent in accordance with the spirit of the Helsinki declaration.

• 2 Healthy male subjects aged = 18 and = 65.

• 3 Weight = 50 kg and = 80 kg, body mass index (BMI) = 18 and = 28kg/m2.

• 4 Each system examination index is within the normal range, or the examination result is abnormal, but it is judged by the researcher to be of no clinical significance.

• 5 The subjects agreed to use reliable contraceptives for themselves and their partners during the study period and within 6 months after the infusion of the study drug(such as abstinence, sterilization, contraceptive pills, injection of contraceptive medroxyprogesterone or subcutaneous implantation contraception, etc).

Exclusion Criteria:

• 1 Have a history of hypertension or abnormal blood pressure during screening / baseline measurement(Repeated measurements on the same day confirmed that systolic blood pressure [SBP] > 140 mmHg and / or diastolic blood pressure [DBP] > 90 mmHg).

• 2 Clinically significant proteinuria (routine urine examination, urine protein 2+ and above) or history of proteinuria assessed by the investigator.

• 3 Have received any antibody or protein therapy targeting VEGF or VEGF receptor in the past 1 year.

• 4 Used any biological products or vaccinated with live virus vaccine within 3 months before the infusion of the study drug, or used any monoclonal antibody within 12 months.

• 5 Have hereditary bleeding tendency or coagulation dysfunction, or have a history of thrombosis or bleeding.

• 6 Have a history of gastrointestinal perforation or fistula.

• 7 Unhealed wound ulcer or fracture, or major surgery within the first 2 months of randomization, or major surgery expected during the study period or within 2 months after the end of the study.

• 8 Use prescription or over-the-counter drugs or nutritional health products, and the use time is within 5 half lives of the drugs or nutritional health products or within 2 weeks before the use of the study drugs (the time limit is whichever is longer).Herbal health products should be stopped 28 days before using the study drug.

• 9 Hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody or syphilis antibody are tested positive.

• 10 Known allergy to bevacizumab or any of its excipients.

• 11 People with known history of allergic diseases or allergic constitution.

• 12 There was a history of blood donation 3 months before the infusion of the study drug.

• 13 Have been treated with any other research drugs or participated in another intervention clinical trial within 2 months before screening.

• 14 Have a history of alcohol or drug abuse within 12 months before screening; The subjects were unable to quit drinking within 72 hours before administration and throughout the trial.

• 15 Have a history of mental illness.

• 16 Subjects whose spouses plan to conceive.

• 17 Unable to follow the protocol requirements to complete the study during the study.

• 18 Other researchers think it is not suitable to be included in the group

Related Conditions & MeSH terms

• Cervical Cancer
• Glioblastoma
• Lung Cancer
• Ovarian Cancer
• Rectal Cancer

Intervention

Drug:
• Bevacizumab injection
Recombinant humanized monoclonal antibody injection against human vascular endothelial growth factor
• Bevacizumab injection(Avastin)
Recombinant humanized monoclonal antibody injection against human vascular endothelial growth factor

Locations

Country	Name	City	State
China	Affiliated Hospital of Changchun University of Traditional Chinese Medicine	Changchun	Jilin

Sponsors (1)

Lead Sponsor	Collaborator
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Plasma concentration-area under time curve(AUC0-t)	Area under the blood concentration time curve from 0 hour to the collection time t of the last measurable concentration	Within 30 minutes before administration to 1680 hours (day 71)
Secondary	Plasma concentration-area under time curve(AUC0-8)	Area under the blood concentration time curve from 0 hour to inf (infinity)	Within 30 minutes before administration to 1680 hours (day 71)
Secondary	Peak concentration (Cmax)	Maximum plasma concentration observed after administration	Within 30 minutes before administration to 1680 hours (day 71)
Secondary	Incidence of adverse events	Incidence of adverse events assessed by CTCAE v4.0	Within 30 minutes before administration to 1680 hours (day 71)
Secondary	Number of adverse events related to the study drug	Number of adverse events evaluated by CTCAE v4.0	Within 30 minutes before administration to 1680 hours (day 71)
Secondary	Incidence of adverse events related to the study drug	Incidence of study drug-related adverse events assessed by CTCAE v4.0	Within 30 minutes before administration to 1680 hours (day 71)
Secondary	ADA positive rate	When anti drug antibody (ADA) is positive, neutralizing antibody (NAB) test is performed	Within 30 minutes before administration to 1680 hours (day 71)