Meningococcal Vaccine Clinical Trial
Official title:
A Randomized Observer-blinded Controlled Non-inferiority Trial to Evaluate the Immunogenicity of Locally Manufactured Meningococcal ACWY Vaccine 'Ingovax ACWY' in Bangladeshi Healthy Adults.
This study will be a randomized observer -blinded controlled non-inferiority study to evaluate and compare the immunogenicity of locally produced Ingovax ACWY with Quadri Meningo on a total of 88 healthy adult participants (18-45 years of age). 44 participants will receive locally produced Ingovax ACWY and 44 participants of comparator groups will receive Quadri Meningo which is produced by BiO-MeD Private Limited. Vaccination will be done in Day 0 following the screening and pre-immunization blood sample collection and post-immunization blood will be collected at Study Day 30. Follow- up by home visit will be carried out from Study day 1-6 and clinic follow-up is scheduled upto Study day 90. The hypothesis of this study is: locally produced subcutaneous Meningococcal vaccine Ingovax ACWY is non inferior and immunogenic among adults in Bangladesh as compared to Quadri Meningo.
Protocol Title: A randomized observer-blinded controlled non-inferiority trial to evaluate
the immunogenicity of locally manufactured Meningococcal ACWY vaccine 'Ingovax ACWY' in
Bangladeshi healthy adults.
Background:
1. Burden:
Meningococcal disease is an infectious disease caused by Neisseria meningitidis or
meningococcus, which may present clinically as meningococcemia or meningitis, or
presence of both features. Meningococcal meningitis causes inflammation of the membranes
covering the brain and spinal cord. Meningococcal meningitis or meningococcemia is a
life-threatening disease. It affects adults, adolescents and children as well. Every
year more than 1.2 million people are affected by meningitis. It causes approximately
120,000 deaths globally each year. It can cause severe brain damage and is fatal in 50%
of cases if untreated. According to a review article on meningococcal disease in Asia,
results from four retrospective hospital-based studies conducted in Bangladesh showed
that N. meningitidis present up to 35% of positive cultures in all ages, and up to 18%
in children aged <2 years with bacterial meningitis. At the International Centre for
Diarrhoeal Disease Research in Bangladesh, of 628 blood and CSF samples, N. meningitidis
was detected in 24•8% (n=156), of which 97•7% were serogroup A and the rest 2.3% were
serogroup B between 1999 and 2006. Of the 156 N. meningitidis isolates, 89 (57%) were
from blood and 67 (43%) from CSF. Meningococcemia occurs without meningitis in 5% to 20%
among the meningococcal infections. Globally the case-fatality ratio of meningococcemia
is up to 40%.
Despite of prompt diagnosis and the availability of appropriate treatments, the diseases
is still a threat to the people. In spite of getting antibiotic in time, one in ten
infected people die within 2 days of their first symptoms, one in four survivors is left
with long-term disabilities such as loss of limb (s), deafness, nervous system problems,
or brain damage. The disease can be transmitted as long as the symptoms persist or until
24 hours of effective treatment have been started. Carriers without symptoms can
transmit the disease for about 6 months. Moreover, the disease can easily spread from
person to person by respiratory droplets of sneezing or coughing or by sharing utensils.
2. Knowledge gap:
Several different bacteria can cause meningitis. Neisseria meningitidis is the one with
the potential to cause large epidemics. There are 12 Serogroups of N. meningitidis that
have been identified, 6 of which (A, B, C, W, X and Y) can cause epidemics. But only a
single dose of vaccine can prevent this deadly disease. Meningococcal Polysaccharide
Vaccine of four serogroups A, C, W and Y that can protect from meningococcal meningitis
and other associated diseases. It is a highly immunogenic and tolerable meningococcal
vaccine to prevent meningococcal disease. World Health Organization recommends that
countries with a moderate or high rate of disease or with frequent outbreaks should
routinely vaccinate. Currently there is no locally manufactured Meningococcal vaccine
available in Bangladesh. The results of this study will provide information regarding
the immunogenicity of the locally manufactured meningococcal vaccine.
3. Relevance:
The study of this locally manufactured Meningococcal Vaccine (Incepta) 'Ingovax ACWY'
among adults will be able to give us information regarding the safety and immunogenicity
of the vaccine. To get registration of this own bulk and finished product, Incepta
intends to conduct clinical trials in human. Incepta has already conducted two
Pre-clinical Studies at Reliance clinical research" in Mumbai, India. Toxicological
evaluation of Meningococcal ACWY Vaccine (Ingovax) was conducted in Swiss albino mice
and Sprague Dawley rats. No mortality or morbidity was observed in any of the animals in
the control or the treated groups. No treatment related abnormal changes were observed
in Clinical Signs, Body Weight, Food Consumption and Ophthalmological Examination. In
the light of the above findings, No Observed Adverse Effect level (NOAEL) of
Meningococcal ACWY Vaccine (Ingovax) is 50µg per rat or mouse. So, after successful
completion of Preclinical study, the non-inferiority trail with this vaccine needs to be
carried out with innovator product and move forward to licensure in Bangladesh.
Currently there is no locally manufactured Meningococcal vaccine available in
Bangladesh. Once this clinical trial is complete, it will then proceed for registration
and licensure in Bangladesh. Thus the vaccine cost could be significantly reduced and
save a large amount of foreign currency of Bangladesh Government.
Hypothesis (if any): Locally produced subcutaneous Meningococcal vaccine Ingovax ACWY is
non inferior and immunogenic among adults in Bangladesh as compared to Menomune® -
A/C/Y/W-135.
Objectives: The objective of this study is to
Primary Objective:
1.To evaluate and compare the immunogenicity of Ingovax ACWY' with Quadri Meningo in
healthy adults in Bangladesh.
Secondary Objective:
1. To evaluate and compare the safety of locally produced Ingovax ACWY with Quadri
Meningo.
Methods:
This will be a randomized observer -blinded controlled non-inferiority study on a total
of 88 healthy adult participants (18-45 years of age). 44 Ingovax ACWY'0.5 ml (Test
group) and 44 Quadri Meningo 0.5 ml (Comparator Group).
Outcome measures/variables: To evaluate and compare the immunogenicity and safety of
locally produced Ingovax ACWY' with Quadri Meningo vaccine.
Primary end points:
1. Assessment of proportion of participants showing seroconversion (defined as a ≥4-fold
rise in SBA titers) vaccinated with either Ingovax ACWY Vaccine (Incepta) or Quadri
Meningo vaccine (BiO-MeD Private Limited). The non-inferiority margin will be 10%.
Secondary end points:
1. To compare the GMTs between vaccines, and GMT ratios.
2. Number of immediate reactions reported within 30 minutes after vaccination
3. Number of solicited adverse events (prelisted in the participant's memory aid)
occurring up to 7 days following vaccination.
4. Number of unsolicited AEs up to 28days after vaccination.
5. Occurrence of serious adverse events (SAEs) throughout the trial
;
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