Trial Assessing the Immunogenicity and Safety of Two Influenza Vaccine Strategies Among Severe Obese Adult Patients

Morbid Obesity Clinical Trial

— FLUO  

Official title:

Multicenter, Randomized, Open, Phase III, Trial Assessing the Immunogenicity and Safety of Two Influenza Vaccine Strategies Among Severe Obese Adult Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05409612
• Other study ID #: APHP200039
• Secondary ID: 2021-002691-39
• Status: Completed
• Phase: Phase 3
• Start date: November 7, 2022
• Est. completion date: October 3, 2023

Study information

• Verified date: January 2024
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

Obese adults are at higher risk of complications and mortality due to influenza infections than healthy adults. The few studies available showed lower vaccine response in obese patients compared to healthy adults and moderate efficacy of standard influenza vaccines among these subjects. Data from the population > 50 years show that a recombinant high dose quadrivalent vaccination strategy improve immunological and clinical efficacy against influenza with comparable rates of local and general solicited reactions. Investigators hypothesize that 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. The primary objective is to assess if the immune response of the new quadrivalent recombinant high-dose influenza vaccine (RIV4) is superior to the current quadrivalent standard dose influenza vaccine (SD) in adult patients with severe obesity in terms of geometric mean titers (GMTs) for each strain at 1 month. The primary endpoint: Ratio (RIV4/SD) of GMTs of each of the 4 strains at 1-month post-vaccination. The ratio of GMTs will be computed by taking the antilog of the difference between means of log-transformed titers. It is a Randomized, open, multicenter, trial in France, evaluating the immunological response and safety of two influenza vaccine strategies using a standard quadrivalent vaccine (Vaxigriptetra®) and the new high-dose recombinant quadrivalent vaccine (Supemtek®). The single administration of influenza vaccine will be performed at D0: Vaxigriptetra® or Supemtek® according to randomization allocation. Three follow-up visits will be performed at M1 and M6 during consultations in the clinical units where participants are usually followed. This multicenter research will involve the participation of the 10 centers in France (metropolitan France and French overseas departments and territories). Each hospital involves a single participating department. All investigational sites belong to the FORCE (national network of clinical research specializing in the study of obesity and associated metabolic diseases) or to the I-REIVAC (Innovative Clinical Research Network In Vaccinology). The duration of recruitment will be 5 months. The duration of participation for each participant will be 6 months, the total duration of the study will be 11 months. For this study, 206 patients will be recruited.

Recruitment information / eligibility

• 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.

Related Conditions & MeSH terms

• Influenza, Human
• Morbid Obesity
• Obesity
• Obesity, Morbid
• Severe Obesity

Intervention

Biological:
• Supemtek®
Quadrivalent recombinant high-dose influenza vaccine containing 45 µg of hemagglutinin (HA) for each of the 4 strains included (2 strains A and 2 strains B). Solution for injection is sterile liquid supplied in 0.5mL single dose pre-filled syringe. Vaccine is injected intra-muscularly in the non-dominant arm at Day 0.
• Vaxigriptetra®
Quadrivalent inactivated influenza vaccine containing 15 µg of hemagglutinin (HA) for each of the 4 strains included. Suspension for injection is sterile liquid supplied in 0.5mL single dose pre-filled syringe. Vaccine is injected intra-muscularly in the non-dominant arm at Day 0.

Locations

Country	Name	City	State
France	Pitie-Salpêtrière hospital APHP	Paris

Sponsors (3)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris	Hospices Civils de Lyon, Sanofi Pasteur, a Sanofi Company

Country where clinical trial is conducted

France, 

Outcome

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