Phase 2a Study of MVA-BN-RSV Vaccination and RSV Challenge in Healthy Adults

RSV Infection Clinical Trial

Official title:

A Phase 2a, Randomised, Double-Blinded, Placebo-Controlled Study to Assess the Safety, Immunogenicity and Efficacy of the Recombinant MVA-BN®-RSV Vaccine Against Respiratory Syncytial Virus Infection in the Virus Challenge Model in Healthy Adult Participants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04752644
• Other study ID #: RSV-MVA-015
• Status: Completed
• Phase: Phase 2
• Start date: February 22, 2021
• Est. completion date: November 2, 2021

Study information

• Verified date: July 2023
• Source: Bavarian Nordic
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Phase 2a, Randomised, Double-Blinded, Placebo-Controlled Study to Assess the Safety, Immunogenicity and Efficacy of the Recombinant MVA-BN®-RSV Vaccine against Respiratory Syncytial Virus Infection in the Virus Challenge Model in Healthy Adult Participants

Recruitment information / eligibility

• Status: Completed
• Enrollment: 73
• Est. completion date: November 2, 2021
• Est. primary completion date: June 17, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

1. An informed consent document signed and dated by the participant and the Investigator 2. Aged between 18 and 50 years old on the day of signing the consent form 3. In good health with no history, or current evidence, of clinically significant medical conditions, and no clinically significant test abnormalities that will interfere with participant safety, as defined by medical history, physical examination, (including vital signs), ECG, and routine laboratory tests as determined by the Investigator 4. A documented medical history prior to enrolment 5. The following criteria are applicable to female participants participating in the study.

1. Females of childbearing potential must have a negative pregnancy test prior to enrolment.

2. Females of non-childbearing potential:

3. Post-menopausal* females; defined as having a history of amenorrhea for >12 months with no alternative medical cause, and /or by FSH level >40mLU/mL, confirmed by laboratory.

4. Documented status as being surgically sterile (hysterectomy, bilateral salpingectomy and bilateral oophorectomyhysterectomy, bilateral salpingectomy and bilateral oophorectomy) 6. The following criteria apply to female and male participants:

a. Female participants of childbearing potential must use one form of highly effective contraception. Hormonal methods must be in place from at least 2 weeks prior to the first study visit. The contraception use must continue until 28 days after the date of viral challenge. Highly effective contraception is as described below: i. Established use of hormonal methods of contraception described below (for a minimum of 2 weeks prior to the first study visit). When hormonal methods of contraception are used, male are required to use a condom with a spermicide: ii. combined (oestrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation:

1. oral 2. intravaginal 3. transdermal iii. progestogen-only hormonal contraception associated with inhibition of ovulation:

1. oral

2. injectable

3. implantable iv. Intrauterine device (IUD) v. Intrauterine hormone-releasing system (IUS) vi. Bilateral tubal ligation vii. Male sterilisation (with the appropriate post vasectomy documentation of the absence of sperm in the ejaculate) where the vasectomised male is the sole partner for that woman.

viii. True abstinence - sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical study and the preferred and usual lifestyle of the participant.

b. Male participants must agree to the contraceptive requirements below from the vaccination visit and continue until 28 days after the date of Viral challenge: i. Use a condom with a spermicide to prevent pregnancy in a female partner or to prevent exposure of any partner (male and female) to the IMP.

ii. Male sterilisation with the appropriate post vasectomy documentation of the absence of sperm in the ejaculate (please note that the use of condom with spermicide will still be required to prevent partner exposure). This applies only to males participating in the study.

iii. In addition, for female partners of childbearing potential, that partner must use another form of contraception such as one of the highly effective methods mentioned above for female participants.

i. True abstinence - sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical study and the preferred and usual lifestyle of the participant.

c. In addition to the contraceptive requirements above, male participants must agree not to donate sperm following discharge from Quarantine until 28 days after the date of Viral Challenge/last dosing with IMP (whichever occurs last).

7. Sero-suitable to the challenge virus, as defined in the study Analytical Plan.

Exclusion Criteria:

1. History of, or currently active, symptoms or signs suggestive of upper or lower respiratory tract infection within 4 weeks prior to the first study visit

2. Any history or evidence of any other clinically significant or currently active systemic comorbidities including psychiatric disorders (includes participants with a history of depression and/or anxiety).

3. And/or other major disease that, in the opinion of the Investigator, may put the participant at undue risk, or interfere with a participant completing the study and necessary investigations (e.g autoimmune disease or immunodeficiency).

4. Participants who have smoked =10 pack years at any time [10 pack years is equivalent to one pack of 20 cigarettes a day for 10 years].

5. A total body weight =50 kg or Body Mass Index (BMI) =18 kg/m2 or =35kg/m2.

6. Females who:

1. Are breastfeeding, or

2. Have been pregnant within 6 months prior to the study.

7. History of anaphylaxis-and/or a history of severe allergic reaction or significant intolerance to any food or drug or vaccine, as assessed by the PI.

8. Venous access deemed inadequate for the phlebotomy and cannulation demands of the study

9. Any significant abnormality altering the anatomy of the nose in a substantial way or nasopharynx that may interfere with the aims of the study and in particular any of the nasal assessments or viral challenge, (historical nasal polyps can be included, but large nasal polyps causing current and significant symptoms and/or requiring regular treatments in the last month will be excluded).

10. Any clinically significant history of epistaxis (large nosebleeds) within the last 3 months of the first study visit and/or history of being hospitalized due to epistaxis on any previous occasion.

11. Any nasal or sinus surgery within 3 months of the first study visit.

Related Conditions & MeSH terms

• Infections
• Respiratory Syncytial Virus Infections
• RSV Infection

Intervention

Biological:
• MVA-mBN294B
MVA-BN-RSV (nominal titre 5 x10*8 Inf.U per 0.5 mL) as intramuscular injections. Liquid frozen suspension, single dose of 0.5ml.

Drug:
• Placebo
TBS (Placebo) as intramuscular injections (0.5ml)

Locations

Country	Name	City	State
United Kingdom	hVIVO Services Limited	London

Sponsors (1)

Lead Sponsor	Collaborator
Bavarian Nordic

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area under the viral load-time curve (VL-AUC) of RSV-A Memphis 37b	Median VL-AUC of RSV-A Memphis 37b as determined by qRT-PCR from nasal washes collected twice daily	From Day 2 post-viral challenge up to discharge from Quarantine (Day12).
Secondary	Peak viral load of RSV-A Memphis 37b	Peak viral load of RSV-A Memphis 37b is defined by the maximum viral load in nasal washes	From Day 2 post-viral challenge up to discharge from Quarantine (Day12).
Secondary	Total clinical symptom score (TSS)	Total clinical symptom score (TSS) determined as the sum of the scores as collected on the participants' symptom diary cards, collected three times daily.	From Day 1 post-viral challenge up to discharge from Quarantine (Day12).
Secondary	Percentage of participants with RT-PCR-confirmed RSV infection	RT-PCR-confirmed RSV infection [at least two detectable (=LLOD) qRT-PCR measurements (reported on 2 or more consecutive days), starting two days post-viral challenge (Day 2) up to discharge from Quarantine], AND 1 or more positive clinical symptoms of Grade 2 or more from any category in the symptom scoring system (Upper Respiratory, Lower Respiratory, Systemic)	From Day 2 up to discharge from Quarantine (Day12)
Secondary	Weight of mucus produced	Median AUC of mucus weight produced	From Day 1 post-viral challenge up to discharge from Quarantine (Day12).
Secondary	Occurrence of solicited local reactions and systemic events	Local reactions (pain, swelling, redness, induration, itching) and systemic events (including body temperature)	From day of vaccination (Day-28) and 7 subsequent days) after vaccination
Secondary	Occurrence of unsolicited adverse events (AEs)	Unsolicited AEs are defined as AEs observed by the participant or investigator which are not pre-listed on the memory aid card/symptom score card	Between vaccination (Day-28) and inoculation with RSV Memphis 37b (Day0)
Secondary	Occurrence of medically attended AEs (MAEs)	A medically attended adverse event (MAE) is an adverse event, whether considered related to the investigational vaccine or not, that led to the participant seeking evaluation by a healthcare provider	From vaccination (Day -28) up to study end (Day 155 (±14 days)).
Secondary	Serious adverse events (SAEs)	SAEs are defined as any untoward medical occurrence that at any dose: results in death, is life threatening, required inpatient hospitalization or prolongation of existing hospitalization, results in persistent disability/incapacity, is a congenital anomaly/birth defect, is an important medical event	From vaccination (Day -28) up to study end (Day 155 (±14 days)).
Secondary	Occurrence of unsolicited AEs	Unsolicited AEs are defined as AEs observed by the participant or investigator which are not pre-listed on the memory aid card/symptom score card	From Day 0 up to Day 28 follow up
Secondary	Occurrence of SAEs	Occurrence of SAEs related to the viral challenge	From Day 0 up to Day 28 follow up

External Links

•   Reduced Respiratory Syncytial Virus Load, Symptoms, and Infections: A Human Challenge Trial of MVA-BN-RSV Vaccine