Morbid Obesity Clinical Trial
— FLUOOfficial title:
Multicenter, Randomized, Open, Phase III, Trial Assessing the Immunogenicity and Safety of Two Influenza Vaccine Strategies Among Severe Obese Adult Patients
Verified date | January 2024 |
Source | Assistance Publique - Hôpitaux de Paris |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Obesity has been considered as a risk factor for mortality and development of complications during infection with the influenza virus. Several case studies of severe and fatal infections have identified possible effects of obesity on disease progression; these effects include extensive viral replication in the deep lung, progression to viral pneumonia, and prolonged and increased viral shedding. These points may be linked to obesity which causes a chronic state of meta-inflammation with systemic implications for immunity: obese patients exhibit delayed and blunted innate and adaptive immune responses to influenza virus infection, and they experience poor recovery from the disease leading to an increased susceptibility to secondary bacterial infections and poor healing of the lung epithelium. Furthermore, in obese people, influenza virus may exploit the lack of antiviral pressure, generate a more virulent population and increase disease severity Due to the growing prevalence of obesity worldwide (500 million subjects in 2017), it is important to be able to offer vaccines that provide the highest protection for this at-risk population. The quadrivalent recombinant high-dose influenza vaccine has been shown to have greater immunogenicity and efficacy than standard influenza vaccine in non-obese adults older than 50 years. However, this vaccine has never been evaluated in obese subjects. Investigators thus planned this trial to assess whether the use of the new quadrivalent recombinant high-dose influenza vaccine (RIV4) will induce a better immunological answer than current quadrivalent standard vaccine (SD) in patients with severe obesity, with an acceptable safety profile, thus leading to a better protection against influenza in this population at high risk of influenza complications.
Status | Completed |
Enrollment | 206 |
Est. completion date | October 3, 2023 |
Est. primary completion date | April 20, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: 1. =18 and =75 years old 2. Body Mass Index (BMI) =35 kg/m2 3. No previous vaccination against influenza (in the preceding 6 months) with either the trial vaccine or another vaccine 4. Absence of health event satisfying the definition of a serious adverse event, or a change in an ongoing drug therapy due to therapeutic failure or symptoms of drug toxicity, within 15 days prior to enrolment. 5. Signed informed consent 6. Participants covered by social security regimen . Exclusion Criteria: 1. Known active infection with HIV and / or HBV (HBs antigen) and / or HCV (RNA positive viral load) 2. Immunodepression or diagnosis of having congenital or acquired immunodeficiency, HIV infection, lymphoma, leukemia, systemic lupus erythematosus, rheumatoid arthritis, juvenile rheumatoid arthritis, inflammatory, bowel disease, or other autoimmune condition 3. Known acute evolving neurological disorder or history of Guillain-Barré syndrome. 4. Moderate or severe acute illness/infection (according to investigator judgment) or febrile illness (tympanic temperature =38°C on the day of vaccination). A subject should not be included in the trial until the condition has resolved or the febrile event has subsided. 5. Proven Influenza infection in the 6 months preceding the study 6. Known systemic hypersensitivity to any of the vaccine components, including a documented allergy to egg proteins, or history of a life-threatening reaction to the vaccines used in the trial or to a vaccine containing any of the same substances. 7. Receipt of any vaccine in the 2 weeks (14 days) preceding the trial vaccination 8. History of bariatric surgery in the 2 years preceding the study. 9. Bariatric surgery planned during the study period. 10. Receipt of immune globulins, blood or blood-derived products in the 3 months preceding the study or planned during the study period. 11. Taking immunosuppressive treatment (including chemotherapy, oral corticosteroids with doses =10 mg/day of prednisone or equivalent during =15 days) or radiotherapy in the 6 months preceding the study or planned during the study. 12. Contraindication to intramuscular injection 13. Female subjects of childbearing potential : - without an adequate contraception (see chapter 5.8) for 30 days prior to vaccination within the context of the study, - breastfeeding - with a positive pregnancy test on the day of vaccination, - did not agreed to continue adequate contraception during 2 months after completion of the vaccination. 14. Participation at the time of trial enrollment (or in the 4 weeks [28 days] preceding the trial vaccination) or planned participation during the present trial period in another clinical trial investigating a vaccine, drug, medical device, or medical procedure 15. Anticipated inability to follow the protocol requirements (e.g. comprehension of the study requirements, ability to comprehend and comply with procedures for collection of safety data, expressed availability for the required study period, and ability and willingness to attend scheduled visits). 16. Participants covered by AME. |
Country | Name | City | State |
---|---|---|---|
France | Pitie-Salpêtrière hospital APHP | Paris |
Lead Sponsor | Collaborator |
---|---|
Assistance Publique - Hôpitaux de Paris | Hospices Civils de Lyon, Sanofi Pasteur, a Sanofi Company |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ratio (RIV4/SD) of geometric mean titers (GMTs) of each of the 4 strains at 1-month post-vaccination.obesity in terms of geometric mean titers (GMTs) for each strain at 1 month. | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers. | 1 month | |
Secondary | seroconversion rate for each of the 4 strains at 1 month after vaccination | defined as pre-vaccination hemagglutination inhibition (HI) titer of <1:10 and post-vaccination titer =1:40 or pre-vaccination HI titer of = 1:10 and a 4-fold post-vaccination rise in antibody titer. Pre-vaccination titers are measured at inclusion and post-vaccination titers at 1 and 6 months after vaccination. | 1 month | |
Secondary | seroconversion rate for each of the 4 strains at 6 month after vaccination | (defined as pre-vaccination hemagglutination inhibition (HI) titer of <1:10 and post-vaccination titer =1:40 or pre-vaccination HI titer of = 1:10 and a 4-fold post-vaccination rise in antibody titer. Pre-vaccination titers are measured at inclusion and post-vaccination titers at 1 and 6 months after vaccination). | 6 month | |
Secondary | seroconversion factor (or geometric mean fold increase) for each of the 4 strains at 1 month after vaccination. | defined as the geometric mean of the within-subject ratios of the post-vaccination reciprocal HI titer to the day 0 reciprocal HI titer | 1 month | |
Secondary | seroconversion factor (or geometric mean fold increase) for each of the 4 strains at 6 month after vaccination. | defined as the geometric mean of the within-subject ratios of the post-vaccination reciprocal HI titer to the day 0 reciprocal HI titer | 6 month | |
Secondary | seroprotection rate defined as the post-vaccination HI titer =1:40 for each of the 4 strains at 1 month after vaccination. | seroprotection rate defined as the post-vaccination HI titer =1:40 for each of the 4 strains at 1 month after vaccination. | 1 month | |
Secondary | seroprotection rate defined as the post-vaccination HI titer =1:40 for each of the 4 strains at 6 month after vaccination. | seroprotection rate defined as the post-vaccination HI titer =1:40 for each of the 4 strains at 6 month after vaccination. | 6 month | |
Secondary | geometric means titers at 6 months after vaccination for each of the 4 strains. | geometric means titers at 6 months after vaccination for each of the 4 strains. | 6 month | |
Secondary | Seroconversion rate of geometric mean titers (GMTs) of each of the 4 strains at 1 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 1 month | |
Secondary | Seroconversion rate of geometric mean titers (GMTs) of each of the 4 strains at 6 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 6 month | |
Secondary | seroconversion factor of geometric mean titers (GMTs) of each of the 4 strains at 1 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 1 month | |
Secondary | seroconversion factor of geometric mean titers (GMTs) of each of the 4 strains at 6 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 6 month | |
Secondary | seroprotection rate of geometric mean titers (GMTs) of each of the 4 strains at 1 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 1 month | |
Secondary | seroprotection rate of geometric mean titers (GMTs) of each of the 4 strains at 6 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 6 month | |
Secondary | ratio (RIV4/SD) of geometric mean titers (GMTs) of each of the 4 strains at 1 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 1 month | |
Secondary | ratio (RIV4/SD) of geometric mean titers (GMTs) of each of the 4 strains at 6 month after vaccination according to class of age (< or = 50 years old) and BMI class ([35-40[ or = 40 kg/m2). | The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers | 6 month | |
Secondary | Number and intensity of solicited reactogenicity events, clinical events within 7 days of vaccination and all other unsolicited adverse event during the study. | reactogenicity events : local (pain, tenderness, induration, redness, swelling) and general (tiredness, chills, joint pain, muscle pain, headache, nausea, fever) | 1 and 6 months | |
Secondary | Identification of the influenza vaccine response determinants in terms of seroconversion for at least two strains after vaccination | considering age, sex, smoking, BMI, chronic conditions (e.g. diabetes mellitus), co-treatments, standard / recombinant vaccine | 1 and 6 months | |
Secondary | Proven influenza cases during the study period. | A proven influenza infection will be defined as a positive influenza RT-PCR performed on a naso-pharyngeal swab at the time of the visit. | 1 and 6 months |
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