A Study of mRNA-1010 Seasonal Influenza Vaccine in Adults 50 Years Old and Older

Sponsor
ModernaTX, Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05566639
Collaborator
(none)
23,000
234
2
18.5
98.3
5.3

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of mRNA-1010 in preventing seasonal influenza in adults 50 years and older.

Condition or Disease Intervention/Treatment Phase
  • Biological: mRNA-1010
  • Biological: Licensed quadrivalent inactivated seasonal influenza vaccine
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
23000 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
A Phase 3, Randomized, Observer-blind, Active-controlled Study to Evaluate the Safety and Efficacy of mRNA-1010 Candidate Seasonal Influenza Vaccine in Adults 50 Years and Older
Actual Study Start Date :
Sep 14, 2022
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Mar 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: mRNA-1010

Participants will receive a single dose of mRNA-1010 by intramuscular (IM) injection on Day 1.

Biological: mRNA-1010
Sterile liquid for injection
Other Names:
  • Seasonal influenza vaccine
  • Active Comparator: Licensed Quadrivalent Inactivated Seasonal Influenza Vaccine

    Participants will receive a single dose of licensed quadrivalent inactivated seasonal influenza vaccine by IM injection on Day 1.

    Biological: Licensed quadrivalent inactivated seasonal influenza vaccine
    Sterile suspension for injection.
    Other Names:
  • Fluarix Tetra
  • Outcome Measures

    Primary Outcome Measures

    1. Number of Solicited Local and Systemic Reactogenicity Adverse Reactions (ARs) [Up to Day 7 (7 days after vaccination)]

    2. Number of Unsolicited Adverse Events (AEs) [Up to Day 28 (28 days after vaccination)]

    3. Number of Serious Adverse Events (SAEs), Adverse Events of Special Interest (AESIs), Medically Attended Adverse Events (MAAEs), and AEs Leading to Discontinuation [Day 1 through Day 361]

    4. Time to First Episode of Reverse Transcription Polymerase Chain Reaction (RT-PCR) Confirmed Protocol-Defined Influenza-Like Illness (ILI) Caused by Any Influenza A or B Virus Strains [14 days post-vaccination through Day 181 or end of influenza season, whichever ends later]

    Secondary Outcome Measures

    1. Time to First Episode of RT-PCR Confirmed Protocol-Defined ILI Caused by Any Influenza A or B Virus Strains with Similarity to the Vaccine Strains [14 days post-vaccination through Day 181 or end of influenza season, whichever ends later]

      Similarity to strains selected for the seasonal vaccine will be determined by antigenicity testing and/or genomic sequencing.

    2. Time to First Episode of RT-PCR Confirmed Protocol-Defined ILI Caused by Any Influenza A or B Virus Strains with Antigenically Matched to the Vaccine Strains [14 days post-vaccination through Day 181 or end of influenza season, whichever ends later]

      Antigenically matched to strains selected for the seasonal vaccine will be determined by antigenicity testing.

    3. Time to First Episode of RT-PCR Confirmed United States (US) Centers for Disease Control and Prevention (CDC)-Defined ILI Caused by Any Influenza A or B Virus Strains [14 days post-vaccination through Day 181 or end of influenza season, whichever ends later]

      Any strains include any influenza A or B strains, influenza A or B strains with similarity to vaccine strains and influenza A or B strains that are antigenically matched to vaccine strains. Antigenically matched to strains selected for the seasonal vaccine will be determined by antigenicity testing.

    4. Time to First Episode of Culture-Confirmed Protocol-Defined ILI Caused by Any Influenza A or B [14 days post-vaccination through Day 181 or end of influenza season, whichever ends later]

      A positive result for influenza infection by viral culture is needed, following a positive result for influenza infection by RT-PCR.

    5. Time to First Episode of Culture-Confirmed CDC-Defined ILI Caused by Any Influenza A or B [14 days post-vaccination through Day 181 or end of influenza season, whichever ends later]

      A positive result for influenza infection by viral culture is needed, following a positive result for influenza infection by RT-PCR

    6. Number of Participants With Hospitalizations Associated With RT-PCR Confirmed Protocol-Defined ILI [14 days post-vaccination through Day 181 or end of influenza season, whichever ends later]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Investigator has assessed that the participant understands and is willing and physically able to comply with protocol mandated follow-up, including all procedures.

    • For female participants of childbearing potential: negative pregnancy test, adequate contraception or has abstained from all activities that could result in pregnancy for at least 28 days prior to the first dose on Day 1, and agreement to continue adequate contraception through 90 days following vaccine administration.

    Exclusion Criteria:
    • Participant has had close contact with someone with laboratory-confirmed influenza infection or with someone who has been treated with antiviral therapies for influenza (for example, Tamiflu®) within the past 5 days prior to the Screening visit.

    • Participant has had close contact to someone with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or COVID-19 as defined by the US CDC or has had a positive SARS-CoV-2 test in the past 10 days prior to the Screening visit.

    • Participant is acutely ill or febrile (temperature ≥38.0℃elcius [100.4°Fahrenheit]) 72 hours prior to or at the Screening visit or Day 1. Participants meeting this criterion may be rescheduled within the 28-day screening window.

    • Participant has a history of a diagnosis or condition that, in the judgment of the investigator, is clinically unstable or may affect participant safety, assessment of safety endpoints, assessment of immune response, or adherence to study procedures.

    • Reported history of congenital or acquired immunodeficiency, immunocompromising/ immunosuppressive condition, asplenia, or recurrent severe infections.

    • Reported history of anaphylaxis or severe hypersensitivity reaction after receipt of any mRNA or influenza vaccines or any components of the mRNA or influenza vaccines, including egg protein.

    • Participant has received systemic immunosuppressant drugs for >14 days in total within 180 days prior to the Screening visit (for glucocorticosteroids, ≥10 milligrams (mg)/day of prednisone or equivalent) or is anticipating the need for systemic immunosuppressive treatment at any time during participation in the study. Inhaled, nasal, and topical steroids are allowed.

    • Participant has received any vaccine authorized or approved by local health agency ≤28 days prior to study intervention (Day 1) or plans to receive a vaccine authorized or approved by local health agency within 28 days before or after the study intervention.

    • Participant is unaware whether they have received an influenza vaccine in the previous influenza season.

    • Participant received a seasonal influenza vaccine or any other investigational influenza vaccine within 180 days prior to Day 1

    • Participant has tested positive for influenza by local health authority-approved testing methods within 180 days prior to Day 1.

    • Participant has donated ≥450 milliliters (mL) of blood products within 28 days prior to the Screening visit or plans to donate blood products during the study.

    Note: Other inclusion and exclusion criteria may apply.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 North Alabama Research Center, LLC Athens Alabama United States 35611
    2 Lenzmeier Family Medicine Glendale Arizona United States 85308
    3 CCT Research Phoenix Arizona United States 85044
    4 Fiel Family and Sports Medicine/CCT Research Tempe Arizona United States 85283
    5 Noble Clinical Research Tucson Arizona United States 85712
    6 Lynn Institute of the Ozarks Little Rock Arkansas United States 72204
    7 Baptist Health Center for Clinical Research Little Rock Arkansas United States 72205
    8 Velocity Clinical Research, Banning Banning California United States 92220
    9 Hope Clinical Research, LLC Canoga Park California United States 91303
    10 Marvel Clinical Research Huntington Beach California United States 92647
    11 Velocity Clinical Research, Chula Vista La Mesa California United States 91942
    12 Velocity Clinical Research, San Diego La Mesa California United States 91942
    13 Velocity Clinical Research - Westlake Los Angeles California United States 90057
    14 Empire Clinical Research Pomona California United States 91767
    15 Artemis Institute for Clinical Research Riverside California United States 92503
    16 Benchmark Research-Texas Riverside California United States 92504-3206
    17 Peninsula Research Associates (PRA) Rolling Hills Estates California United States 90274
    18 Artemis Institute for Clinical Research San Diego California United States 92103
    19 Women's Health Care Research Corp. San Diego California United States 92111
    20 Acclaim Clinical Research San Diego California United States 92120
    21 Medical Center for Clinical Research San Diego California United States 92120
    22 Shawn K Hassler MD San Francisco California United States 94102-3014
    23 West Coast Research LLC San Ramon California United States 94582
    24 Velocity Clinical Research, Denver Denver Colorado United States 80209
    25 Arthritis & Rheumatology - Clinic of Northern Colorado Fort Collins Colorado United States 80528
    26 Longmont Medical Research Network Longmont Colorado United States 80501
    27 Nature Coast Clinical Research, LLC - Crystal River Crystal River Florida United States 34429
    28 Floridian Clinical Research Hialeah Florida United States 33016
    29 Homestead Associates in Research,Inc Hialeah Florida United States 33016
    30 Broward Research Group Hollywood Florida United States 33024
    31 Citrus Cardiology Consultants Inverness Florida United States 34452
    32 Encore Research Group-Jacksonville Center for Clinical Resea Jacksonville Florida United States 32216
    33 Health Awareness, Inc Jupiter Florida United States 33458
    34 Multi-Therapeutic Research Associates, Inc. Lake City Florida United States 32055
    35 Accel Research Sites - Lakeland Lakeland Florida United States 33805
    36 ARS - Meridien Research Maitland Florida United States 32751
    37 Global Health Research Center Miami Lakes Florida United States 33016
    38 South Florida Research Center, Inc. Miami Florida United States 33135
    39 Suncoast Research Associates Trials, LLC Miami Florida United States 33135
    40 Miami centre of clinical research Miami Florida United States 33155
    41 Clinical Trials of Florida, LLC Miami Florida United States 33186
    42 Innovation Medical Research Center,inc Palmetto Bay Florida United States 33157
    43 New Tampa Health, Inc Tampa Florida United States 33603
    44 Tekton Research, Inc. Chamblee Georgia United States 30341
    45 Southeast Regional Research Group Columbus Georgia United States 31904
    46 iResearch Atlanta, LLC Decatur Georgia United States 30030
    47 In-Quest Medical Research Norcross Georgia United States 30092-4544
    48 Mount Vernon Clinical Research Sandy Springs Georgia United States 30328
    49 Meridian Clinical Research - Savannah Savannah Georgia United States 31406-2675
    50 Clinical Research Atlanta Stockbridge Georgia United States 30281-9054
    51 Velocity Clinical Research - Boise Meridian Idaho United States 83642
    52 Great Lakes Clinical Trials LLC Chicago Illinois United States 60625
    53 Great Lakes Clinical Trials LLC Chicago Illinois United States 60640
    54 Great Lakes Clinical Trials LLC Gurnee Illinois United States 60031
    55 Chicago Health Medical Group River Forest Illinois United States 60305
    56 Velocity Clinical Research - Valparaiso Valparaiso Indiana United States 46385
    57 Meridian Clinical Research - Dakota Dunes Sioux City Iowa United States 51106
    58 Johnson County Clin-Trials (JCCT) Lenexa Kansas United States 66219
    59 Heartland Research Associates LLC Newton Kansas United States 67114-9017
    60 Alliance for Multispecialty Research Wichita Kansas United States 67207
    61 Meridian Clinical Research Baton Rouge Louisiana United States 70809
    62 MedPharmics Covington Louisiana United States 70433
    63 Medpharmics, LLC Metairie Louisiana United States 70006
    64 Nathan H Fischman MD LLC New Orleans Louisiana United States 70124
    65 Privia Medical Group Annapolis Maryland United States 21401
    66 Rockville Internal Medicine Group Rockville Maryland United States 20854-2957
    67 Delricht Research Springfield Massachusetts United States 65807-7303
    68 DM Clinical Research - Detroit Southfield Michigan United States 48076
    69 Paul G Matherne MD Biloxi Mississippi United States 39531
    70 DELRICHT RESEARCH at GULFPORT MEMORIAL Gulfport Mississippi United States 39503
    71 Sundance Clinical Research, LLC Saint Louis Missouri United States 63141
    72 National Medical University and Embryonic Tissues Center EmC Springfield Missouri United States 65802
    73 Montana Medical Research, Inc Missoula Montana United States 59808
    74 CCT Research at Skyline Medical Center, PC Elkhorn Nebraska United States 68022
    75 CCT Research / Methodist Physicians Clinic, Prairie Fields Family Medicine, PC Fremont Nebraska United States 68025-2592
    76 Meridian Clinical Research Grand Island Nebraska United States 68803
    77 Be Well Clinical Studies, LLC Lincoln Nebraska United States 68516
    78 Medpace, Inc. - Clinical Pharmacology Unit (CPU) Norfolk Nebraska United States 68701
    79 Meridian Clinical Research Norfolk Nebraska United States 68701
    80 Papillon Research Centre Omaha Nebraska United States 68130
    81 Meridian Clinical Research - Omaha Omaha Nebraska United States 68134
    82 Midwest Regional Health Services, LLC/CCT Research Omaha Nebraska United States 68144-5225
    83 CCT Research Las Vegas Nevada United States 89102-1682
    84 Clinical Research Center of Nevada LLC Las Vegas Nevada United States 89104
    85 Santa Rosa Medical Centers of Nevada/ CCT Research Las Vegas Nevada United States 89119
    86 Las Vegas Clinical Trials, LLC North Las Vegas Nevada United States 89030
    87 United Medical Associates Binghamton New York United States 13901-1043
    88 Rochester Clinical Research, Inc Rochester New York United States 14609
    89 Velocity Clinical Research - Syracuse Syracuse New York United States 13057
    90 Tryon Medical Group Charlotte North Carolina United States 28210
    91 Carolina Institute for Clinical Research Fayetteville North Carolina United States 28303
    92 Diabetes & Endocrinology Consultants Morehead City North Carolina United States 28557
    93 M3 Wake Research, Inc. Raleigh North Carolina United States 27612
    94 PMG Research of Wilmington Wilmington North Carolina United States 28401
    95 Trial Management Associates Wilmington North Carolina United States 28403
    96 Wake Forest Baptist Medical Center Winston-Salem North Carolina United States 27157
    97 Radiant Research Akron Ohio United States 44311
    98 Sterling Research Group Cincinnati Ohio United States 45219
    99 CTI Clinical Research Center Cincinnati Ohio United States 45227
    100 Velocity Clinical Research - Cincinnati Cincinnati Ohio United States 45242
    101 Lynn Health Science Institute Oklahoma City Oklahoma United States 73112
    102 Delricht Research Tulsa Tulsa Oklahoma United States 74133
    103 Platinum Research Network, LLC Yukon Oklahoma United States 73099
    104 Platinum Research Network, LLC Yukon Oklahoma United States 73099
    105 Velocity Clinical Research - Grants Pass Grants Pass Oregon United States 97520
    106 Velocity Clinical Resarch - Medford Medford Oregon United States 97504
    107 Velocity Clinical Research - Providence Warwick Rhode Island United States 02886
    108 Velocity Clinical Research, Greenville Anderson South Carolina United States 29621
    109 Velocity Clinical Research - Columbia Columbia South Carolina United States 29204
    110 Velocity Clinical Research, Gaffney Gaffney South Carolina United States 29340
    111 Velocity Clinical Research - Greenville Greenville South Carolina United States 29615
    112 Carolina Health Specialists Myrtle Beach South Carolina United States 29572
    113 Spartanburg Regional Health Services Spartanburg South Carolina United States 29303
    114 Black Hills Center for American Indian Health Rapid City South Dakota United States 57701
    115 Delricht Research Hendersonville Tennessee United States 37075
    116 Tekton Research, Inc Austin Texas United States 78745
    117 Platinum Research Network, LLC Beaumont Texas United States 77706
    118 Zenos Clinical Research Dallas Texas United States 75230-2505
    119 Benchmark Research Fort Worth Texas United States 76135
    120 DM Clinical Research Houston Texas United States 77065
    121 Texas Center for Drug Development, Inc. Houston Texas United States 77081
    122 DELRICHT RESEARCH at ZOMNIR FAMILY MEDICINE McKinney Texas United States 75070
    123 Research Your Health Plano Texas United States 75093
    124 Epic Medical Research, LLC Red Oak Texas United States 75154
    125 Clinical Trials of Texas, Inc San Antonio Texas United States 78229
    126 DM Clinical Research Sugar Land Texas United States 77478
    127 Breco Research - A Tarheel Clinical Research Site Sugar Land Texas United States 77479
    128 Cope Family Medicine Bountiful Utah United States 84010
    129 Olympus Family Medicine/CCT Research Holladay Utah United States 84117
    130 CenExel - JBR Salt Lake City Utah United States 84107
    131 South Ogden Family Medicine clinic/CCT South Ogden Utah United States 84405-4869
    132 Velocity Clinical Research - Salt Lake City West Jordan Utah United States 84088
    133 Meridian Clinical Research Portsmouth Virginia United States 23703-3200
    134 Clinical Research Partners, LLC Richmond Virginia United States 23226
    135 Lakeview Medical Center Suffolk Virginia United States 23435
    136 MHAT Sveti Ivan Rilski Kozloduy Bulgaria
    137 MC City Clinic Sveti Georgi - Montana Montana Bulgaria
    138 MHAT "Dr. Stamen Iliev Montana Bulgaria
    139 Medical Center Medconsult Pleven Pleven Bulgaria
    140 Military Medical Academy Sofia Bulgaria
    141 SHAT of Pneumo-phthisiatric diseases - Sofia District Sofia Bulgaria
    142 Aggarwal and Associates LTD Brampton Canada
    143 Aviva Clinical Trials Group Inc Burlington Canada
    144 Hamilton Medical Research Group Hamilton Canada
    145 Okanagan Clinical Trials Kelowna Canada
    146 Centricity Research Quebec City Levis Canada
    147 Milestone Research Inc. London Canada
    148 Yang Medicine Ottawa Canada
    149 LMC Manna Pointe-Claire Canada
    150 DIEX Research Quebec Inc. Quebec Canada G1G 3Y8
    151 DIEX Research Quebec Inc. Quebec Canada G1N 4V3
    152 Alpha Recherche Clinique Inc Quebec Canada
    153 Clinique de Lebourgneuf Quebec Canada
    154 Clinique spécialisée en allergie - Allergy/Immunology/Asthma/Mpoc Quebec Canada
    155 Diex Research Sherbrooke Inc Quebec Canada
    156 Central Alberta Research Clinic Red Deer Canada
    157 Diex Recherche - Joilette - HyperCore - PPDS Saint-Charles-Borromée Canada
    158 Glencar Medical Inc. Sarnia Canada
    159 Canadian Phase Onward Inc. Toronto Canada
    160 LMC Toronto Canada
    161 Manna Research Toronto Canada
    162 Medicine Professional Corporation Toronto Canada
    163 Toronto Western Hospital Toronto Canada
    164 Diex Recherche Trois-Rivières Trois-Rivieres Canada
    165 Colchester East Hants Health Authority - Colchester Regional Truro Canada
    166 Diex Recherche Victoriaville Victoriaville Canada
    167 Odense University Hospital Odense Denmark
    168 Sjællands UniHosp, Roskilde - Medicine and Infectious Diseases Roskilde Denmark
    169 Aarhus Universitetshospital Århus N Denmark
    170 Center for Clinical and Basic Research Tallinn Estonia
    171 Innomedica OÜ Tallinn Estonia
    172 Merelahe Family Doctors Centre Tallinn Estonia
    173 Clinical Research Center Tartu Estonia
    174 Berliner Centrum für Reise- und Tropenmedizin Berlin Germany
    175 Emovis GmbH Berlin Germany
    176 Klinische Forschung Berlin-Mitte GmbH Berlin Germany
    177 Klinische Forschung Berlin Berlin Germany
    178 Klinische Forschung Dresden GmbH Dresden Germany
    179 Medizentrum Essen Borbeck Essen Germany
    180 Studienzentrum Dr. Keller Frankfurt/Main Germany
    181 IKF Pneumologie Frankfurt Germany
    182 Infektiologikum Frankfurt-Sachsenhausen Frankfurt Germany
    183 Clinical Research Hamburg GmbH Hamburg Germany
    184 Klinische Forschung Hamburg GmbH Hamburg Germany
    185 Klinische Forschung Hannover-Mitte GmbH Hannover Germany
    186 Siteworks GmbH Hannover Germany
    187 Siteworks GmbH Heidelberg Germany
    188 University Hospital Cologne AöR Köln Germany
    189 Synexus Clinical Research GmbH Leipzig Germany
    190 Praxis Illies Magdeburg Germany
    191 Dermatologie Quist Mainz Germany
    192 Praxis Schaum Oldenburg Germany
    193 Klinische Forschung Schwerin GmbH Schwerin Germany
    194 Hautarztpraxis Leitz & Kollegen Stuttgart Germany
    195 Studienzentrum Brinkum Wardenburg Germany
    196 Leids Universitair Medisch Centrum (LUMC) Leiden Netherlands
    197 Universitair Medisch Centrum (UMC) Utrecht - Julius Center for Health Sciences and Primary Care Utrecht Netherlands
    198 Centrum Medyczne Pratia Bydgoszcz Bydgoszcz Poland
    199 Centrum Medyczne Plejady Krakow Poland
    200 Krakowskie Centrum Medyczne Sp. z o.o. Kraków Poland
    201 Centrum Medyczne AMED Oddzial w Lodzi Lodz Poland
    202 ETG Lublin Lublin Poland
    203 KO-MED Centra Kliniczne Lublin II Lublin Poland
    204 ETG Skierniewice Skierniewice Poland
    205 Centrum Innowacyjnych Terapii Sp. z o.o. Warszawa Poland
    206 Provita Centrum Medyczne Sp. z o.o. Warszawa Poland
    207 RCMed Warszawa Poland
    208 ETG Zamosc Zamosc Poland
    209 KO-MED Centra Kliniczne Sp. z o.o. Zamosc Poland
    210 Hospital de Antequera Antequera Spain
    211 Hospital Clinic De Barcelona Barcelona Spain
    212 Hospital Santa Creu i Sant Pau - Research institut Barcelona Spain
    213 Universitat Autonoma de Barcelona (UAB) - Institut d'Investigacio en Atencio Primaria Jordi Gol (IDIAP Jordi Gol) Barcelona Spain
    214 Hospital Alvaro Cunqueiro Vigo Spain
    215 Hospital Povisa Vigo Spain
    216 Kaohsiung Veterans General Hospital Kaohsiung City Taiwan
    217 China Medical University Hospital - division of Rheumatology - Taichung Taichung Taiwan
    218 National Cheng Kung University hospital Tainan Taiwan
    219 National Taiwan University Hospital - Family Medicine Taipei Taiwan
    220 Taipei Medical University - Taipei Medical University Hospital Taipei Taiwan
    221 Taipei Medical University - WanFang Hospital Taipei Taiwan
    222 Tri-Service General Hospital - Neihu Branch - Infectious Diseases Taipei Taiwan
    223 Royal United Hospital Bath United Kingdom
    224 Layton Medical Centre Blackpool United Kingdom
    225 Hull University Teaching Hospitals NHS Foundation trust Hull United Kingdom
    226 University Hospitals of Leicester-Leicester Royal Hospital Leicester United Kingdom
    227 Liverpool University Hospitals NHS Foundation Trust - Aintree University Hospital (Fazakerley Hospital) Liverpool United Kingdom
    228 GST NHS Found London United Kingdom
    229 Newcastle University - Institute of Cellular Medicine (ICM) Newcastle United Kingdom
    230 Panthera Biopartners - Manchester - multispeciality Rochdale United Kingdom
    231 Panthera Biopartners - Sheffield - multispeciality Rochdale United Kingdom
    232 Panthera Biopartners - Preston - multispeciality Salford United Kingdom
    233 Southampton General Hospital Southampton United Kingdom
    234 Royal Cornwall Hospitals Trust - Respiratory Truro United Kingdom

    Sponsors and Collaborators

    • ModernaTX, Inc.

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    ModernaTX, Inc.
    ClinicalTrials.gov Identifier:
    NCT05566639
    Other Study ID Numbers:
    • mRNA-1010-P302
    • 2022-001638-12
    First Posted:
    Oct 4, 2022
    Last Update Posted:
    Oct 4, 2022
    Last Verified:
    Sep 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by ModernaTX, Inc.
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 4, 2022