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Virus Therapy
mRNA Vaccines for Flu and COVID-19
Phase 1 & 2
Waitlist Available
Research Sponsored by ModernaTX, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Are you 65–79 years of age?
In general, do you consider yourself to be in good health?
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (day 1) to day 29, and day 181
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new vaccine called mRNA-1083 in adults aged 18 to 79 years old. The vaccine uses a small piece of genetic material to help the body recognize and fight off the flu.
Who is the study for?
This trial is for healthy adults aged 65–79 who've completed their initial COVID-19 vaccine series at least 4 months ago and haven't had a flu shot in the last 5 months. Participants must be willing to attend up to 5 visits and take about 4 calls over roughly 7 months.
What is being tested?
The study tests several mRNA-based vaccines against influenza and COVID-19, including new formulations like mRNA-1283.222, to find the best composition and dose for future larger trials.
What are the potential side effects?
Potential side effects may include typical reactions seen with vaccinations such as soreness at injection site, fatigue, headache, muscle pain, chills or fever. Each individual's reaction can vary.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline (day 1) to day 29, and day 181
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (day 1) to day 29, and day 181
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Part 2: Influenza: Percentage of Participants with Seroconversion at Day 29, as Measured by HAI Assay
Part 2: SARS-CoV-2: Percentage of Participants with Seroresponse at Day 29, as Measured by PsVNA
Secondary study objectives
Part 1: Influenza: Percentage of Participants with Seroconversion, as Measured by HAI Assay
Part 1: SARS-CoV-2: Percentage of Participants with Seroresponse, as Measured by PsVNA
Part 2: Influenza: Percentage of Participants with Seroconversion at Day 181, as Measured by HAI Assay
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
37Treatment groups
Experimental Treatment
Active Control
Group I: Part 2: mRNA-1083 Composition 2 Dose DExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 2 at Dose Level D on Day 1.
Group II: Part 2: mRNA-1083 Composition 2 Dose CExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 2 at Dose Level C on Day 1.
Group III: Part 2: mRNA-1083 Composition 2 Dose BExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 2 at Dose Level B on Day 1.
Group IV: Part 2: mRNA-1083 Composition 2 Dose AExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 2 at Dose Level A on Day 1.
Group V: Part 2: mRNA-1083 Composition 1 Dose DExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 1 at Dose Level D on Day 1.
Group VI: Part 2: mRNA-1083 Composition 1 Dose CExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 1 at Dose Level C on Day 1.
Group VII: Part 2: mRNA-1083 Composition 1 Dose BExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 1 at Dose Level B on Day 1.
Group VIII: Part 2: mRNA-1083 Composition 1 Dose AExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083 Composition 1 at Dose Level A on Day 1.
Group IX: Part 1 Cohort B7: mRNA-1083.3Experimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.3 on Day 1.
Group X: Part 1 Cohort B6: mRNA-1083.2 Dose CExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.2 at Dose Level C on Day 1.
Group XI: Part 1 Cohort B5: mRNA-1083.2 Dose BExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.2 at Dose Level B on Day 1.
Group XII: Part 1 Cohort B4: mRNA-1083.2 Dose AExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.2 at Dose Level A on Day 1.
Group XIII: Part 1 Cohort B3: mRNA-1083.1 Dose CExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.1 at Dose Level C on Day 1.
Group XIV: Part 1 Cohort B2: mRNA-1083.1 Dose BExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.1 at Dose Level B on Day 1.
Group XV: Part 1 Cohort B1: mRNA-1083.1 Dose AExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.1 at Dose Level A on Day 1.
Group XVI: Part 1 Cohort A7: mRNA-1083.3Experimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.3 on Day 1.
Group XVII: Part 1 Cohort A6: mRNA-1083.2 Dose CExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.2 at Dose Level C on Day 1.
Group XVIII: Part 1 Cohort A5: mRNA-1083.2 Dose BExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.2 at Dose Level B on Day 1.
Group XIX: Part 1 Cohort A4: mRNA-1083.2 Dose AExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.2 at Dose Level A on Day 1.
Group XX: Part 1 Cohort A3: mRNA-1083.1 Dose CExperimental Treatment1 Intervention
Participants will receive single IM injection of mRNA-1083.1 at Dose Level C on Day 1.
Group XXI: Part 1 Cohort A2: mRNA-1083.1 Dose BExperimental Treatment1 Intervention
Participants will receive single intramuscular (IM) injection of mRNA-1083.1 at Dose Level B on Day 1.
Group XXII: Part 2: Influenza Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of Influenza Vaccine 1 on Day 1.
Group XXIII: Part 1 Cohort A12: Influenza Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of Influenza Vaccine 1 on Day 1.
Group XXIV: Part 1 Cohort A13: Influenza Vaccine 2Active Control1 Intervention
Participants will receive single IM injection of Influenza Vaccine 2 on Day 1.
Group XXV: Part 1 Cohort B8: Investigational Influenza Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of Investigational Influenza Vaccine 1 on Day 1.
Group XXVI: Part 1 Cohort A10: COVID-19 Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of COVID-19 Vaccine 1 on Day 1.
Group XXVII: Part 2: Investigational COVID-19 Vaccine 2Active Control1 Intervention
Participants will receive single IM injection of Investigational COVID-19 Vaccine 2 on Day 1.
Group XXVIII: Part 1 Cohort A9: Investigational COVID-19 Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of Investigational COVID-19 Vaccine 1 on Day 1.
Group XXIX: Part 1 Cohort A11: Investigational Influenza Vaccine 2Active Control1 Intervention
Participants will receive single IM injection of Investigational Influenza Vaccine 2 on Day 1.
Group XXX: Part 1 Cohort B9: Investigational COVID-19 Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of Investigational COVID-19 Vaccine 1 on Day 1.
Group XXXI: Part 1 Cohort B10: COVID-19 Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of COVID-19 Vaccine 1 on Day 1.
Group XXXII: Part 1 Cohort B11: Investigational Influenza Vaccine 2Active Control1 Intervention
Participants will receive single IM injection of Investigational Influenza Vaccine 2 on Day 1.
Group XXXIII: Part 2: COVID-19 Vaccine 2Active Control1 Intervention
Participants will receive single IM injection of COVID-19 Vaccine 2 on Day 1.
Group XXXIV: Part 1 Cohort A8: Investigational Influenza Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of Investigational Influenza Vaccine 1 on Day 1.
Group XXXV: Part 2: Investigational Influenza Vaccine 1 Dose BActive Control1 Intervention
Participants will receive single IM injection of Investigational Influenza Vaccine 1 at Dose Level B on Day 1.
Group XXXVI: Part 2: Investigational Influenza Vaccine 1 Dose AActive Control1 Intervention
Participants will receive single IM injection of Investigational Influenza Vaccine 1 at Dose Level A on Day 1.
Group XXXVII: Part 1 Cohort B12: Influenza Vaccine 1Active Control1 Intervention
Participants will receive single IM injection of Influenza Vaccine 1 on Day 1.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
mRNA-1083
2023
Completed Phase 3
~8080
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
mRNA vaccines, such as the mRNA-1083, instruct cells to produce a protein that triggers an immune response, helping the body recognize and fight the virus. Monoclonal antibodies target the virus directly, while antiviral drugs like remdesivir inhibit viral replication.
Steroids reduce inflammation caused by the immune response, and anticoagulants prevent blood clots, a common complication in severe COVID-19 cases. Understanding these mechanisms is crucial for COVID-19 patients as it helps tailor treatments to different stages and severities of the disease, improving outcomes.
Current Therapeutics for COVID-19, What We Know about the Molecular Mechanism and Efficacy of Treatments for This Novel Virus.TLR4 as a therapeutic target for respiratory and neurological complications of SARS-CoV-2.An update on drugs with therapeutic potential for SARS-CoV-2 (COVID-19) treatment.
Current Therapeutics for COVID-19, What We Know about the Molecular Mechanism and Efficacy of Treatments for This Novel Virus.TLR4 as a therapeutic target for respiratory and neurological complications of SARS-CoV-2.An update on drugs with therapeutic potential for SARS-CoV-2 (COVID-19) treatment.
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
ModernaTX, Inc.Lead Sponsor
118 Previous Clinical Trials
61,584,008 Total Patients Enrolled
40 Trials studying COVID-19
61,380,624 Patients Enrolled for COVID-19
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Would you be able and willing to participate in to up to 5 in-person visits and about 4 phone calls over a time period of up to 7 months?Are you 65–79 years of age?In general, do you consider yourself to be in good health?Have you completed the two-dose COVID-19 vaccine primary series?Have you not received a COVID-19 vaccine within the last 4 months?Have you not received a seasonal flu vaccine within the last 5 months?
Research Study Groups:
This trial has the following groups:- Group 1: Part 1 Cohort B7: mRNA-1083.3
- Group 2: Part 1 Cohort A2: mRNA-1083.1 Dose B
- Group 3: Part 1 Cohort A6: mRNA-1083.2 Dose C
- Group 4: Part 2: mRNA-1083 Composition 1 Dose C
- Group 5: Part 2: Influenza Vaccine 1
- Group 6: Part 2: mRNA-1083 Composition 2 Dose A
- Group 7: Part 1 Cohort A7: mRNA-1083.3
- Group 8: Part 1 Cohort A12: Influenza Vaccine 1
- Group 9: Part 1 Cohort A13: Influenza Vaccine 2
- Group 10: Part 1 Cohort A3: mRNA-1083.1 Dose C
- Group 11: Part 1 Cohort B8: Investigational Influenza Vaccine 1
- Group 12: Part 1 Cohort A10: COVID-19 Vaccine 1
- Group 13: Part 2: mRNA-1083 Composition 2 Dose C
- Group 14: Part 2: Investigational COVID-19 Vaccine 2
- Group 15: Part 1 Cohort B4: mRNA-1083.2 Dose A
- Group 16: Part 1 Cohort A9: Investigational COVID-19 Vaccine 1
- Group 17: Part 1 Cohort A4: mRNA-1083.2 Dose A
- Group 18: Part 1 Cohort A11: Investigational Influenza Vaccine 2
- Group 19: Part 1 Cohort B1: mRNA-1083.1 Dose A
- Group 20: Part 1 Cohort B2: mRNA-1083.1 Dose B
- Group 21: Part 2: mRNA-1083 Composition 1 Dose D
- Group 22: Part 1 Cohort B6: mRNA-1083.2 Dose C
- Group 23: Part 2: mRNA-1083 Composition 1 Dose A
- Group 24: Part 1 Cohort B9: Investigational COVID-19 Vaccine 1
- Group 25: Part 1 Cohort B10: COVID-19 Vaccine 1
- Group 26: Part 1 Cohort B11: Investigational Influenza Vaccine 2
- Group 27: Part 2: COVID-19 Vaccine 2
- Group 28: Part 1 Cohort A8: Investigational Influenza Vaccine 1
- Group 29: Part 1 Cohort B3: mRNA-1083.1 Dose C
- Group 30: Part 2: mRNA-1083 Composition 1 Dose B
- Group 31: Part 1 Cohort A5: mRNA-1083.2 Dose B
- Group 32: Part 2: Investigational Influenza Vaccine 1 Dose B
- Group 33: Part 2: Investigational Influenza Vaccine 1 Dose A
- Group 34: Part 1 Cohort B5: mRNA-1083.2 Dose B
- Group 35: Part 1 Cohort B12: Influenza Vaccine 1
- Group 36: Part 2: mRNA-1083 Composition 2 Dose B
- Group 37: Part 2: mRNA-1083 Composition 2 Dose D
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
COVID-19 Patient Testimony for trial: Trial Name: NCT05827926 — Phase 1 & 2
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