Tuberculosis
Conditions
Keywords
Tuberculosis, Vaccine
Brief summary
The safety, tolerability and immunogenicity of lyophilized recombinant tuberculosis vaccine (AEC/BC02) were studied in a randomized, blind, controlled phase ⅱ A clinical study in patients 18 years and older with latent infection of Mycobacterium tuberculosis.Twenty patients with negative control group and 180 patients with latent mycobacterium tuberculosis infection were divided into sentinel group, placebo group, high-dose adjuvant group, low-dose vaccine group, high-dose vaccine group and high-dose vaccine group (three doses).During the test, each subject shall not change groups or receive drugs.The negative control group did not take chemical drugs and did not get vaccinated after enrollment, and was only used as immunogenicity control.The latent infection group was given orally Koch inhibitor chemical drugs (Ifu tablet or Ifu capsule) or placebo twice a week, and then received placebo, adjuvant or vaccine every two weeks (0-2-4-6-8-10 weeks), with a total of 6 doses injected intramuscular alternately in the left and right arms of the upper arm deltoid muscle.
Interventions
Subjects receive low-dose freeze-dried recombinant tuberculosis vaccine (AEC / BC02) injection into the deltoid muscle of the upper arm
BIOLOGICALHigh-dose freeze-dried recombinant tuberculosis vaccine (AEC / BC02)
Subjects receive high-dose freeze-dried recombinant tuberculosis vaccine (AEC / BC02) injection into the deltoid muscle of the upper arm
BIOLOGICALHigh-dose adjuvant for freeze-dried recombinant tuberculosis vaccine (AEC / BC02)
Subjects receive high-dose adjuvant for freeze-dried recombinant tuberculosis vaccine (AEC / BC02) injection into the deltoid muscle of the upper arm
Subjects receive Lyophilized recombinant tuberculosis vaccine (AEC / BC02) placebo injection into the deltoid muscle of the upper arm
Sponsors
Anhui Zhifei Longcom Biologic Pharmacy Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. The age is 18 years old and above, and the gender is not limited; 2. I agree to participate in this study and sign the informed consent; 3. I can complete the whole process of clinical research in accordance with the requirements of the clinical research program; 4. Vital signs (reference range of normal values of vital signs: systolic blood pressure \<160 mmHg and diastolic blood pressure \<100 mmHg (which can be controlled by taking medicine), pulse 60-100 beats/min, axillary temperature \<37.3 ℃ in a quiet state), Physical examination results show no abnormality or abnormality without clinical significance; 5. Negative control population: the test results are EC- and PPD- (the average diameter of EC skin test induration and flush is less than 5mm, and the PPD skin test induration is less than 5mm), and the chest imaging is normal; 6. People with latent infection of Mycobacterium tuberculosis: the test result is EC+ (EC skin test induration or flush ≥5mm), and the chest imaging is normal; 7. Laboratory tests including blood routine, urine routine, blood biochemistry and other tests are all normal or have no clinical significance; 8. There is no abnormality in the electrocardiogram examination or the abnormality has no clinical significance; 9. Those who have no history of tuberculosis after medical history inquiry.
Exclusion criteria
1. Those who are currently diagnosed with tuberculosis or have a history of tuberculosis and/or tuberculosis treatment; 2. There are serious chronic diseases or the disease is in the advanced stage and cannot be controlled smoothly, such as diabetes and thyroid disease; 3. Currently suffering from or within 2 years of any of the following serious diseases, such as: advanced tumor, autoimmune disease, progressive atherosclerosis, acute exacerbation of chronic obstructive pulmonary disease, acute or progressive liver or kidney disease, congestive heart failure exhaustion, etc.; 4. Those with known or suspected (or high-risk) immune function impairments or abnormalities, such as those receiving systemic glucocorticoids, immunosuppressants or immunosuppressants within 3 months, and within 3 months Those who received protein preparations or blood products or plasma extracts outside the gastrointestinal tract; 5. Existing mental/neurological diseases or history of mental/neurological diseases: those with convulsions, epilepsy, encephalopathy, or family history of mental illness; 6. Those who currently suffer from biliary obstruction; 7. People with allergic constitution, such as those with a history of allergy to two or more drugs or foods; a history of severe allergy to any component of the test vaccine, such as: anaphylactic shock, allergic laryngeal edema, allergic purpura, thrombocytopenia Purpura, dyspnea, angioedema, etc.; or a history of the above-mentioned serious side effects after using any vaccine or drug in the past; a history of allergy to isoniazid tablets, rifampicin and rifamycin antibiotics; 8. Patients with severe liver insufficiency, or patients with drug-induced hepatitis and acute liver disease caused by any cause; 9. Difficulty swallowing, active or clinically significant digestive system diseases, and affecting drug absorption; 10. Current patients with active viral hepatitis and/or HIV antibody positive for human immunodeficiency virus and/or current or past syphilis; 11. Women who are pregnant, breastfeeding, or have a positive urine pregnancy test during the screening period, or before vaccination, or who have childbearing plans during the study period; 12. Those who are vaccinated with inactivated vaccine within 14 days before oral administration of chemical drugs, and those who are vaccinated with live attenuated vaccine within 30 days; 13. Those who have participated in any other clinical research and used the investigational drug within 3 months before this clinical research; 14. Any other situation that the researcher believes may affect the evaluation of the research.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The number of adverse events after intramuscular injection | Up to 6 months after the sixth time injection | The observation of adverse events mainly come from vital sign detection and laboratory examination (including blood routine/urine routine/blood biochemistry/electrocardiogram and chest X-ray), local reactions and systemic reactions after injection. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Laboratory markers of immunity | Up to 3 months after the sixth time injection | Changes in the levels of antigen-specific total IgG antibodies and IgG subclasses (IgG1 and IgG2). |
Countries
China
Outcome results
None listed