Non- Inferiority Fractional-doses Trial for Yellow Fever Vaccine
Keywords
Abstract
Description
Yellow fever (YF) is a disease caused by a mosquito-borne flavivirus that is endemic in sub-Saharan Africa and tropical South America. Ninety percent of YF cases are in Africa where YF virus is transmitted by different mosquito genera in three recognized transmission cycles. A sylvatic cycle involves transmission between forest-dwelling mosquitoes (Haemagogus spp) and non-human primate reservoirs, with sporadic incidental transmission to humans (e.g. forest workers). An intermediate cycle, occurring only in Africa, involves mosquito transmission between non-human primates and humans, or human-to-human transmission among humans living or working close to forested areas. An urban cycle involves transmission between humans and urban mosquito vectors, primarily Aedes aegypti, and occurs when a viraemic person, infected in the sylvatic or intermediate cycle, introduces YF virus to areas with a large non-immune population and A. aegypti vectors resulting in disease outbreaks.
Infection with YF virus is characterised by a wide range of manifestations, ranging from subclinical infection with mild and non-specific symptoms, to severe, life-threatening illness with jaundice, renal failure and haemorrhage.
A highly effective vaccine is available for use against YF in adults and children aged ≥9 months. The vaccine is a freeze-dried preparation of live attenuated YF virus strain 17D, which was developed in 1937 and is produced by four WHO-prequalified manufacturers. A single dose of YF vaccine is considered sufficient to confer life-long protective immunity against all seven known genotypes of wild-type YF virus. Protective levels of YF virus neutralizing antibodies are developed in 80-100% vaccine recipients within 10 days after vaccination, and in 99% within a month.
Although fractional dosing has recently been used in vaccination campaigns in Kinshasa and Brazil in 2016, 2017 and 2018, WHO recommendations were based on a limited number of clinical studies and important data gaps remain.
fractional vaccine dosing is compounded by the uncertainty surrounding minimum dose requirements.
This study therefore aims to determine the lowest dose in International Units (IU/dose) that is non-inferior to the standard full dose among populations in sub-Saharan Africa. The data generated in this study will provide information regarding the re-definition of the minimal dose and potency requirements of the vaccine. The study will also provide further confidence in the use of fractional doses of YF vaccine during epidemics. In addition, the investigators will assess the range of views and perceptions of key stakeholders in vaccine policy and implementation on reduced vaccine dose usage during YF epidemics and for routine use.
. The study will be conducted at the KEMRI CGMRC in Kilifi, Kenya and at Epicentre in Mbarara, Uganda. Both these sites are already working together in an ongoing study (ClinicalTrials.gov number: NCT02991495).
Adult participants (n=480) will be randomized for vaccination with full standard dose or with 1000, 500 or 250 IU (i.e. 4 arms) with a 1:1:1:1 allocation ratio. Results for the safety and primary outcome of the adult study will then be reviewed by the DSMB, and the lowest non-inferior dose in the adult study selected for assessment in children aged 9 months to 5 years (n=420) in comparison to full standard dose (i.e. 2 arms) with a 1:1 allocation ratio. The determination of the non-inferior dose to use in children will be made by the sponsor in discussion with the study Data Safety and Monitoring Board (DSMB), vaccine manufacturer and relevant stakeholders, and the final decision communicated to the various regulatory authorities as a notification (i.e. Scientific and Ethics Review Board (SERU) at KEMRI, Oxford Tropical Research Ethics Committee (OxTREC) and Pharmacy and Poisons board (PPB) for the Kilifi site, Mbarara University of Science and Technology's Research Ethics Committee (MUST-REC), Uganda National Council of Science and Technology (UNCST) and National Drug Authority (NDA) for the Mbarara site).
Adult vaccinees will be followed up for 2 years, and children for 1 year. There will be no gradual age de-escalation on the basis that there are few safety concerns with the full dose of YF vaccines, having been used in millions of children worldwide.
Dates
| Last Verified: | 07/31/2019 |
| First Submitted: | 07/25/2019 |
| Estimated Enrollment Submitted: | 08/14/2019 |
| First Posted: | 08/15/2019 |
| Last Update Submitted: | 08/14/2019 |
| Last Update Posted: | 08/15/2019 |
| Actual Study Start Date: | 08/11/2019 |
| Estimated Primary Completion Date: | 12/30/2021 |
| Estimated Study Completion Date: | 04/29/2022 |
Condition or disease
Intervention/treatment
Biological: Yellow fever vaccine, Institut Pasteur
Phase
Arm Groups
| Arm | Intervention/treatment |
|---|---|
| Active Comparator: Standard Dose Yellow fever vaccine, Institut Pasteur, standard dose as release by manufacturer will be administered subcutaneously once. | |
| Experimental: Fractional dose (1000 IU/dose) Yellow fever vaccine, Institut Pasteur, will be titrated to about 1000IU/dose and administered subcutaneously once. | |
| Experimental: Fractional dose (500 IU/dose) Yellow fever vaccine, Institut Pasteur, will be titrated to about 500IU/dose and administered once. | |
| Experimental: Fractional dose (250 IU/dose) Yellow fever vaccine, Institut Pasteur, will be titrated to about 250IU/dose and administered once. |
Eligibility Criteria
| Ages Eligible for Study | 9 Months To 9 Months |
| Sexes Eligible for Study | All |
| Accepts Healthy Volunteers | Yes |
| Criteria | Inclusion Criteria: - Individuals aged ≥18 - <60 years of age. - Children aged between 9 months and 5 years. - HIV negative on serological screening OR HIV positive adults and children aged > 18 months on serological testing, and no symptoms suggestive of current clinical immunosuppression and cluster of differentiation-4 (CD4) count>200 (for adults) and CD4% > 25% (for children aged <5 years) within the last 6 months. - Ability to provide informed consent to participate in the study Exclusion Criteria: - Known contraindications to YF vaccination such as allergies to egg protein and chicken products or any component of the vaccine (including gelatin, eggs, eggs products or chicken products), immunodeficiency, known thymus disorder, such as thymoma and myasthenia gravis - Using corticosteroids or other immunosuppressive therapy - Thymus disorder, such as thymoma and myasthenia gravis - Acute febrile disease on the day of vaccination with temperature >37.5 degrees Celsius is a temporal contraindication. - Previous YF vaccination - Previous YF infection as determined from history - Pregnancy (as determined by a urine test on the proposed day of vaccination) and lactating women - Planning to migrate out of the study areas before the end of the study follow-up - Planning to travel to a country requiring YF vaccination certificate within the first year after vaccination. - Any condition or criteria, including acute or chronic clinically significant abnormality that in the opinion of the investigator might compromise the wellbeing of the volunteer or interfere with the outcome of the study. |
Outcome
Primary Outcome Measures
1. The proportion of vaccinees that seroconverts as measured by Plaque Reduction Neutralisation Test (PRNT-50) [28 days post vaccination]
Secondary Outcome Measures
1. Duration of immunity as measured by PRNT [10 days, 28 days, 1 year and 2 years (adults)]
2. Change in the geometric mean fold of the antibody titre as measured by PRNT [Baseline and 28 days after vaccination]
3. Other flavivirus antibodies interference as tested by neutralisation tests [Baseline and 28 days after vaccination]
4. Post-vaccination viremia as measured by quantitative Polymerase Chain Reaction (PCR) [baseline, and on days 2, 3, 4, 5, 6, 7 and 10 after vaccination]
5. Changes in cellular immunology [baseline and days 10 and 28 post-vaccination.]
6. Changes in biomarkers [Baseline, and on days 2, 3, 4, 5, 6, 7,10 and 28 after vaccination]
7. Safety of different doses as described by the occurrence of adverse events (AE) and serious adverse events. [28 days after vaccination and an average of 1 year for the adult study and two years for the children study. .]
