The pivotal Phase 3 trial plans to enroll a total of approximately 12,460 participants aged 50+ over two years. Participants will be immunized twice with the M-001 universal influenza vaccine candidate or placebo and then followed for up to 2 seasons. The trial will evaluate the number of influenza cases in each group and the severity of illness during the follow up period.
The placebo-controlled pivotal clinical efficacy Phase 3 trial plans to enroll a total of approximately 12,460 participants over two years. Participants will be immunized twice with the M-001 influenza vaccine candidate or placebo. Influenza incidence and illness severity will be evaluated throughout the follow-up period of up to two years. Participants will be 50 years and older, with at least half over 65 years of age. The trial is expected to take place in eastern European countries and begin prior to the 2018/19 Northern Hemisphere flu season.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
12,460
Jagiellońskie Centrum Innowacji Sp.z o.o.
Krakow, Ul. Bobrzyńskiego 14,, Poland
Jagiellońskie Centrum Innowacji Sp.z o.o.
Krakow, Poland
Number of Participants With qRT-PCR or Culture-confirmed Influenza-like Illness
Prevention of influenza disease by comparing the occurrence of either qRT-PCR or culture confirmed influenza in the M-001 experimental group vs. placebo caused by any influenza A or B virus in association with a protocol defined Influenza Like Illness.
Time frame: From Day 14 post-second vaccination day to end of influenza season, an average of 4 months per participant per year
Number of Participants With One or More Serious Adverse Events, New Onset Chronic Illness, and Non-solicited Adverse Events
Number of participants with one or more Serious Adverse Events, New Onset Chronic illness, and Non-solicited Adverse Events assessed during one flu season per participant
Time frame: From Day 0 to end of study completion by participant which coincides with end of flu season in the respective year, an average of 4 months per participant per year
Number of Participants With Culture-confirmed Influenza Incidence
Occurrence of culture confirmed influenza in the M-001 experimental group vs. placebo caused by any influenza A or B virus in association with a protocol defined Influenza Like Illness.
Time frame: From Day 14 post-second vaccination day to end of influenza season, an average of 4 months per participant per year
Number of Participants With Reduction of Severity of qRT-PCR or Culture-confirmed Influenza
Assessed by reduction of severity of either qRT-PCR or culture-confirmed influenza illness by the reduction due to M-001 in the average number of days with respiratory or systemic symptoms during the first laboratory-confirmed influenza illness episode.
Time frame: From Day 14 post-second vaccination day to end of influenza season, an average of 4 months per participant per year
Number of Participants With Influenza-like Illness Symptoms
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Assessment of number of participants having ILI symptoms in the experimental or control group
Time frame: From Day 14 post-second vaccination day to end of influenza season, an average of 4 months per participant per year