MedPath

Study of Recombinant Protein Vaccines With Adjuvant as a Primary Series and as a Booster Dose Against COVID-19 in Adults 18 Years of Age and Older

Phase 2
Completed
Conditions
COVID-19
Interventions
Biological: SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 3
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 4
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage B
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 2
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage A
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 3
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 1
Biological: SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 1
Biological: SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 2
Biological: SARS-CoV-2 adjuvanted recombinant protein vaccine, bivalent (D614+B.1.351)-AS03
Registration Number
NCT04762680
Lead Sponsor
Sanofi Pasteur, a Sanofi Company
Brief Summary

The primary objectives of the study are:

To assess the safety profile of the study vaccines in each study intervention group.

To assess the neutralizing antibody profile after primary series vaccination in SARS-CoV-2-naïve adults.

To demonstrate that a booster dose of monovalent or bivalent SARS-CoV-2 vaccine given to adults previously vaccinated with an authorized/approved COVID-19 vaccine induces an immune response that is non-inferior to the response induced by a twodose priming series with the monovalent vaccine, and superior to that observed immediately before booster.

The secondary objectives of the study are:

To assess the neutralizing and binding antibody profiles after primary series vaccination at pre-defined time points during the study.

To assess the neutralizing and binding antibody responses of booster vaccination.

To describe the occurrences of laboratory-confirmed symptomatic COVID19 after primary series and booster vaccination.

To describe the occurrences of serologically-confirmed SARS-CoV-2 infection after primary series vaccination.

Detailed Description

The duration of each participant's participation in the study will be approximately:

Original Phase 2 part: 365 days postinjection 2 (ie, 386 days total). Supplemental Cohorts 1 and 2: 365 days post-booster injection (ie, 366 days total).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3385
Inclusion Criteria

-Aged 18 years or older on the day of inclusion. - -A female participant is eligible to participate if she is not pregnant or breastfeeding and one of the following conditions applies: Is of non-childbearing potential. To be considered of non-childbearing potential, a female mut be post-menopausal for at least 1 year or surgically sterile.

OR Is of childbearing potential and agrees to use an effective contraceptive method or abstinence from at least 4 weeks prior to the first vaccination until at least 12 weeks after the last vaccination (ie, second dose of primary series or booster injection). A participant of childbearing potential must have a negative highly sensitive pregnancy test (urine or serum as required by local regulation) within 4 hours before any dose of study intervention. - -Informed consent form has been signed and dated.

Able to attend all scheduled visits and to comply with all study procedures. SARS-CoV-2 rapid serodiagnostic test performed at the time of enrollment to detect presence of SARS-CoV-2 antibodies (Original Phase 2 Cohort).

For persons living with human immunodeficiency virus (HIV), stable HIV infection determined by participant currently on antiretrovirals with CD4 count > 200/mm3.

Does not intend to receive an authorized/approved COVID-19 vaccine from first vaccination to 3 weeks after the second vaccination despite encouragement by the investigator to receive the authorized vaccine available to them at the time of enrollment.

Supplemental cohorts: for participants originally enrolled in the Phase II cohort of the study, informed consent has to be signed and dated for transitioning to Supplemental Cohort 2.

Supplemental cohorts, Booster arms: received a complete primary vaccination series with an authorized/conditionally approved mRNA COVID-19 vaccine (mRNA-1273 [Moderna] or BNT162b2 [Pfizer/BioNTech]) or adenovirus-vectored COVID-19 vaccine (ChAdOx1 nCoV-19 [Oxford University/AstraZeneca] or Ad26.CoV2.S [J&J/Janssen]), with the last dose administered a minimum of 4 months prior to inclusion but not longer than 10 months prior to inclusion.

Exclusion Criteria

-Known systemic hypersensitivity to any of the vaccine components, or history of a life-threatening reaction to a vaccine containing any of the same substances.

Dementia or any other cognitive condition at a stage that could interfere with following the trial procedures based on Investigator or designee's judgment.

Self-reported thrombocytopenia, contraindicating intramuscular (IM) vaccination based on Investigator's judgment.

Bleeding disorder, or receipt of anticoagulants in the past 21 days preceding inclusion, contraindicating IM vaccination based on Investigator's judgment.

Unstable acute or chronic illness that in the opinion of the Investigator or designee poses additional risk as a result of participation or that could interfere with the study procedures.

Receipt of solid-organ or bone marrow transplants in the past 180 days. Receipt of anti-cancer chemotherapy in the last 90 days. Receipt of immunoglobulins, blood, or blood-derived products in the past 3 months.

Moderate or severe acute illness/infection (according to investigator judgment) on the day of vaccination or febrile illness (temperature ≥ 38.0°C [≥ 100.4°F]). A prospective participant should not be included in the trial until the condition has resolved or the febrile event has subsided. Receipt of any vaccine in the 30 days preceding or on the day of the first study vaccination or planned receipt of any vaccine between the first study vaccination and in the 30 days following the second study vaccination except for influenza vaccination, which may be received at any time in relation to study intervention.

Applicable to Original Phase II Cohort, Supplemental Cohort 1 and Cohort 2 Comparator Group: Prior administration of a coronavirus vaccine (SARS-CoV-2, SARS-CoV, Middle East Respiratory Syndrome [MERS-CoV]). Participation at the time of study enrollment (or in the 30 days preceding the first study vaccination) or planned participation during the present study trial period in another clinical study investigating a vaccine, drug, medical device, or medical procedure. Exclusion criterion for the Supplemental Cohort 1 and Cohort 2 comparator group: positive rapid diagnostic test for SARS-CoV-2 antibodies at time of enrollment.

Exclusion criterion for participants in Supplemental Cohort 2 who were primed as participant in the Original Phase II Cohort of the present study: Receipt of authorized/conditionally approved COVID-19 vaccine after enrollment in Original Phase 2 Cohort.

Exclusion criterion for all Booster groups: Documented virologically-confirmed SARS-CoV-2 infection (by NAAT) after first dose of primary immunization.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Phase 2 Cohort - SARS-CoV-2 vaccine Formulation 3SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 32 injections of SARS-CoV-2 vaccine Formulation 3 Day 1 and Day 22
Supplemental Cohort 2 - Booster Monovalent (B.1.351)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA or adenovirus-vector COVID-19 vaccine or SARS-Cov-2 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Cohort 2 - Booster Exploratory 4SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 4Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Supplemental Comparator for Cohort 1 and 2 Boosters - Monovalent (D614)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage B2 injections of monovalent (D614)-AS03 SARS-CoV-2 vaccine at Day 1 and Day 22 in previously unvaccinated, naïve participants
Cohort 2 - Booster Exploratory 2SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 2Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Supplemental Cohort 1 - Booster Monovalent (D614)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage AParticipants who were previously vaccinated 4 to \< 10 months prior with an authorized mRNA or adenovirus-vector COVID-19 vaccine will receive 1 booster injection of monovalent (D614)-AS03 SARS-CoV-2 vaccine
Cohort 2 - Booster Exploratory 3SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 3Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Supplemental Cohort 2 - Booster Monovalent (D614)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage AParticipants who were vaccinated 4 to \< 10 months prior with SARS-Cov-2 vaccine will receive 1 booster injection of monovalent (D614)-AS03 SARS-CoV-2 vaccine
Cohort 2 - Booster Exploratory 1SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 1Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Phase 2 Cohort -SARS-CoV-2 vaccine Formulation 1SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 12 injections of SARS-CoV-2 vaccine Formulation 1 at Day 1 and Day 22
Phase 2 Cohort - SARS-CoV-2 vaccine Formulation 2SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 22 injections of SARS-CoV-2 vaccine Formulation 2 at Day 1 and Day 22
Supplemental Cohort 2 - Booster Bivalent (D614 + B.1.351)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, bivalent (D614+B.1.351)-AS03Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA or adenovirus-vector COVID-19 vaccine will receive 1 booster injection of bivalent (D614+B.1.351)-AS03 SARS-CoV-2 vaccine
Phase 2 Cohort -SARS-CoV-2 vaccine Formulation 1SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 12 injections of SARS-CoV-2 vaccine Formulation 1 at Day 1 and Day 22
Phase 2 Cohort - SARS-CoV-2 vaccine Formulation 2SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 22 injections of SARS-CoV-2 vaccine Formulation 2 at Day 1 and Day 22
Phase 2 Cohort - SARS-CoV-2 vaccine Formulation 3SARS-CoV-2 recombinant protein vaccine Phase 2 Formulation 32 injections of SARS-CoV-2 vaccine Formulation 3 Day 1 and Day 22
Supplemental Cohort 1 - Booster Monovalent (D614)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage AParticipants who were previously vaccinated 4 to \< 10 months prior with an authorized mRNA or adenovirus-vector COVID-19 vaccine will receive 1 booster injection of monovalent (D614)-AS03 SARS-CoV-2 vaccine
Supplemental Cohort 2 - Booster Monovalent (B.1.351)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA or adenovirus-vector COVID-19 vaccine or SARS-Cov-2 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Supplemental Cohort 2 - Booster Bivalent (D614 + B.1.351)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, bivalent (D614+B.1.351)-AS03Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA or adenovirus-vector COVID-19 vaccine will receive 1 booster injection of bivalent (D614+B.1.351)-AS03 SARS-CoV-2 vaccine
Supplemental Cohort 2 - Booster Monovalent (D614)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage AParticipants who were vaccinated 4 to \< 10 months prior with SARS-Cov-2 vaccine will receive 1 booster injection of monovalent (D614)-AS03 SARS-CoV-2 vaccine
Supplemental Comparator for Cohort 1 and 2 Boosters - Monovalent (D614)-AS03 SARS-CoV-2 vaccineSARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (D614)-AS03, Dosage B2 injections of monovalent (D614)-AS03 SARS-CoV-2 vaccine at Day 1 and Day 22 in previously unvaccinated, naïve participants
Cohort 2 - Booster Exploratory 1SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 1Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Cohort 2 - Booster Exploratory 2SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 2Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Cohort 2 - Booster Exploratory 3SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 3Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Cohort 2 - Booster Exploratory 4SARS-CoV-2 adjuvanted recombinant protein vaccine, monovalent (B.1.351)-AS03 Alternative Exploratory Formulation 4Participants who were vaccinated 4 to \< 10 months prior with an authorized mRNA COVID-19 vaccine will receive 1 booster injection of monovalent (B.1.351)-AS03 SARS-CoV-2 vaccine
Primary Outcome Measures
NameTimeMethod
Presence of unsolicited adverse eventsWithin 21 days after vaccination

Adverse events other than solicited reactions.

Presence of immediate adverse eventsWithin 30 minutes after vaccination

Immediate adverse events include unsolicited adverse events occurring within 30 minutes after injection.

Presence of solicited injection site or systemic reactionsWithin 7 days after vaccination

Injection site reactions: injection site pain, erythema and swelling. Systemic reactions: fever, headache, malaise and myalgia.

Presence of adverse events of special interestFrom Day 1 to Day 387

Adverse events of special interest are reported throughout the study.

Responders, as determined by neutralizing antibody titers at Day 36From Day 1 to Day 36

Responders, defined as participants who had baseline values below lower limit of quantification (LLOQ) with detectable neutralization titer above assay LLOQ at each pre-defined time point and participants with baseline values above LLOQ with a 4-fold increase in neutralizing antibody titer at Day 36

Presence of serious adverse eventsFrom Day 1 to Day 387

Serious adverse events are reported throughout the study.

Neutralizing antibody titer at Day 36Day 36

Neutralizing antibody titers are expressed as geometric mean titers.

Neutralizing antibody titer at Day 36 (Cohorts 1 and 2 Comparator Group)Day 36

Neutralizing antibody titers are expressed as geometric mean titers.

2-fold rise and 4-fold-rise in neutralization antibody titerFrom Day 1 to Day 36

Fold-rise in antibody neutralization titer post-vaccination relative to Day 1.

Neutralizing antibody titer at Day 15 (post-booster injection)Day 15 (post-booster injection)

Neutralizing antibody titers are expressed as geometric mean titers.

Presence of medically-attended adverse eventsFrom Day 1 to Day 387

Medically-attended adverse events are new onset or a worsening of a condition that prompts the participant or participant's parent/guardian to seek unplanned medical advice at a physician's office or Emergency Department.

Neutralizing antibody titer fold-rise post-vaccinationFrom Day 1 to Day 36

Neutralizing antibody titer fold-rise post-vaccination.

Neutralizing antibody titer at Day 1Day 1

Neutralizing antibody titers are expressed as geometric mean titers.

Neutralizing antibody titer at Day 1 (pre-booster injection)Day 1 (pre-booster injection)

Neutralizing antibody titers are expressed as geometric mean titers.

Responders, as determined by neutralizing antibody titers at Day 36 (Cohorts 1 and 2 Comparator Group)From Day 1 to Day 36

Responders are defined as participants with a 4-fold-or greater rise in serum neutralization titer \[pre/post\] at Day 36 relative to Day 1

Secondary Outcome Measures
NameTimeMethod
Binding antibody concentrationsDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387
Responders, as determined by binding antibody concentrationsDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387

Responders are defined as participants who had baseline values below LLOQ with detectable anti concentration above assay LLOQ at each pre-defined time point and participants with baseline values above LLOQ with a 4-fold increase in anti-S antibody concentration at each pre-defined time point.

Binding antibody fold-riseDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387

Fold-rise in concentration relative to Day 1.

Occurrences of laboratory-confirmed symptomatic COVID-19From Day 1 to Day 387

Symptomatic COVID-19 is defined as laboratory-confirmed SARS-CoV-2 infection accompanied by protocol-defined COVID-19-like illness. Laboratory-confirmed SARS-CoV-2 infection is defined as a positive result for SARS CoV-2 by nucleic acid amplification test (NAAT), done by the central laboratory or locally, on at least one respiratory sample.

Occurrences of severe symptomatic COVID-19From Day 1 to Day 387

Symptomatic COVID-19 is defined as laboratory-confirmed SARS-CoV-2 infection accompanied by protocol-defined COVID-19-like illness with pre-defined criteria of severity.

Occurrences of serologically-confirmed SARS-CoV-2 infectionFrom Day 1 to Day 387

Serologically-confirmed SARS-CoV-2 infection is defined as a positive result in a serum sample for antibodies against SARS-CoV-2.

2-fold rise and 4-fold-rise in neutralization antibody titer at all pre-defined time points post-booster and booster comparator injectionDay 1 and Day 15 -post-booster injection) and Day 36

Neutralizing antibody titer fold-rise post-vaccination.

2-fold rise and 4-fold-rise in neutralization antibody titer at all pre-defined time pointsDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387

Fold-rise in antibody neutralization titer post-vaccination relative to Day 1.

2-fold-rise and 4-fold rise in binding antibody concentrationDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387

Fold-rise in concentration relative to Day 1.

Binding antibody concentrations post-booster injectionDay 1, Day 15, Day 29, Day 91, Day 181, and Day 366 (post-booster injection)
Neutralizing antibody titer at all pre-defined time pointsDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387
Neutralizing antibody titer fold-rise post-vaccination at all pre-defined time pointsDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387

Fold-rise in antibody neutralization titer post-vaccination relative to Day 1.

Responders, as determined by neutralizing antibody titers at each pre-defined time pointDay 1, Day 22, Day 36, Day 78, Day 134, Day 202, Day 292 and Day 387

Responders, defined as participants who had baseline values below LLOQ with detectable neutralization titer above assay LLOQ at each pre-defined time point and participants with baseline values above LLOQ with a 4-fold increase in neutralizing antibody titer at each pre-defined timepoint.

Occurrences of death associated with symptomatic COVID-19From Day 1 to Day 387

Symptomatic COVID-19 is defined as laboratory-confirmed SARS-CoV-2 infection accompanied by protocol-defined COVID-19-like illness.

Seroresponse rate post-booster and booster comparator injectionDay 1 and Day 15 (post-booster injection) and Day 36

Seroresponse rate is defined as the percentage or participants with 4-fold-or greater rise in serum neutralization titer \[pre/post\] at post-vaccination relative to pre-vaccination.

Occurrences of symptomatic COVID-19 episodes associated with hospitalizationFrom Day 1 to Day 387

Symptomatic COVID-19 is defined as laboratory-confirmed SARS-CoV-2 infection accompanied by protocol-defined COVID-19-like illness.

Neutralizing antibody titer at all pre-defined time points post-booster and booster comparator injectionDay 1 and Day 15 (post-booster injection) and Day 36
Binding antibody fold-rise post-booster injectionDay 1, Day 15, Day 29, Day 91, Day 181, and Day 366 (post-booster injection)

Fold-rise in concentration relative to Day 1.

2-fold-rise and 4-fold rise in binding antibody concentration post-booster injectionDay 1, Day 15, Day 29, Day 91, Day 181, and Day 366 (post-booster injection)

Fold-rise in concentration relative to Day 1.

Neutralizing antibody titer fold-rise post-vaccination at all pre-defined time points post-booster and booster comparator injectionDay 1 and Day 15 (post-booster injection) and Day 36

Neutralizing antibody titer fold-rise post-vaccination.

Trial Locations

Locations (66)

Investigational Site Number : 2500007

🇫🇷

Pierre Benite, France

Investigational Site Number : 2500004

🇫🇷

Rennes, France

Investigational Site Number : 2500002

🇫🇷

Tours Cedex 1, France

Investigational Site Number : 3400002

🇭🇳

Municipio Del Distrito Central, Honduras

Investigational Site Number : 3400001

🇭🇳

San Pedro Sula, Honduras

Synexus - Clinical Research Advantage, Inc. Site Number : 8400270

🇺🇸

Birmingham, Alabama, United States

Synexus Chandler Site Number : 8400251

🇺🇸

Chandler, Arizona, United States

Synexus - Glendale. Site Number : 8400271

🇺🇸

Glendale, Arizona, United States

Baptist Health Center for Clinical Research Site Number : 8400077

🇺🇸

Little Rock, Arkansas, United States

Charles R. Drew University of Medicine and Science Site Number : 8400220

🇺🇸

Los Angeles, California, United States

Peninsula Research Associates, Inc. Site Number : 8400094

🇺🇸

Rolling Hills Estates, California, United States

Optimal Research Site Number : 8400173

🇺🇸

San Diego, California, United States

Yale University Site Number : 8400239

🇺🇸

New Haven, Connecticut, United States

The George Washington University Site Number : 8400212

🇺🇸

Washington, District of Columbia, United States

Cenexel Research Centers of America Site Number : 8400089

🇺🇸

Hollywood, Florida, United States

Optimal Research, LLC Site Number : 8400057

🇺🇸

Melbourne, Florida, United States

Synexus Clinical Research US, Inc. - Orlando Site Number : 8400179

🇺🇸

Orlando, Florida, United States

Emory University Decatur Site Number : 8400201

🇺🇸

Decatur, Georgia, United States

Chicago Clinical Research Institute, Inc. Site Number : 8400269

🇺🇸

Chicago, Illinois, United States

Optimal Research Site Number : 8400187

🇺🇸

Peoria, Illinois, United States

Synexus Clinical Research Evansville Site Number : 8400272

🇺🇸

Evansville, Indiana, United States

Research Works INC Site Number : 8400045

🇺🇸

New Orleans, Louisiana, United States

Optimal Research, LLC Rockville Site Number : 8400048

🇺🇸

Rockville, Maryland, United States

Brigham and Women's Hospital Site Number : 8400199

🇺🇸

Boston, Massachusetts, United States

Synexus St. Louis Site Number : 8400100

🇺🇸

Saint Louis, Missouri, United States

Velocity Clinical Research, Omaha Site Number : 8400030

🇺🇸

Omaha, Nebraska, United States

Holy Name Medical Center Site Number : 8400072

🇺🇸

Teaneck, New Jersey, United States

NYU VC-Augustana Site Number : 8400267

🇺🇸

Brooklyn, New York, United States

New York University Langone Vaccine Center Site Number : 8400230

🇺🇸

New York, New York, United States

Columbia University Irving Medical Center Site Number : 8400203

🇺🇸

New York, New York, United States

University of Rochester Site Number : 8400207

🇺🇸

Rochester, New York, United States

University of Pittsburgh Site Number : 8400233

🇺🇸

Pittsburgh, Pennsylvania, United States

Coastal Carolina Research Center Site Number : 8400097

🇺🇸

North Charleston, South Carolina, United States

American Indian Clinical Trials Research Network Site Number : 8400204

🇺🇸

Rapid City, South Dakota, United States

AES Austin Site Number : 8400191

🇺🇸

Austin, Texas, United States

Investigational Site Number : 0360001

🇦🇺

South Brisbane, Queensland, Australia

Investigational Site Number : 0360003

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Norwood, Australia

Investigational Site Number : 0360002

🇦🇺

Southport, Australia

Investigational Site Number : 0360005

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Westmead, Australia

Investigational Site Number : 0360004

🇦🇺

Woodville, Australia

Investigational Site Number : 2500013

🇫🇷

Dijon, France

Investigational Site Number : 2500008

🇫🇷

Limoges, France

Investigational Site Number : 2500014

🇫🇷

Lyon, France

Investigational Site Number : 2500015

🇫🇷

Marseille, France

Investigational Site Number : 2500016

🇫🇷

Marseille, France

Investigational Site Number : 2500006

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Nantes, France

Investigational Site Number : 2500005

🇫🇷

Paris, France

Investigational Site Number : 2500003

🇫🇷

Pessac, France

Investigational Site Number : 5540005

🇳🇿

New Lynn, Auckland, New Zealand

Investigational Site Number : 5540002

🇳🇿

Christchurch, New Zealand

Investigational Site Number : 5540007

🇳🇿

Nawton, New Zealand

Investigational Site Number : 5540010

🇳🇿

Nelson, New Zealand

Investigational Site Number : 5540001

🇳🇿

Rotorua, New Zealand

Investigational Site Number : 7240013

🇪🇸

Santiago De Compostela, Galicia [Galicia], Spain

Investigational Site Number : 7240016

🇪🇸

Majadahonda, Madrid, Spain

Investigational Site Number : 7240009

🇪🇸

Madrid, Spain

Investigational Site Number : 7240008

🇪🇸

Valencia, Spain

Investigational Site Number : 7240003

🇪🇸

Vigo, Spain

Investigational Site Number : 8260011

🇬🇧

Runcorn, Halton, United Kingdom

Investigational Site Number : 8260017

🇬🇧

Bath, Somerset, United Kingdom

Investigational Site Number : 8260013

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Surrey, Sutton, United Kingdom

Investigational Site Number : 8260014

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Doncaster, United Kingdom

Investigational Site Number : 8260016

🇬🇧

Gloucester, United Kingdom

Investigational Site Number : 8260010

🇬🇧

Harrow, United Kingdom

Investigational Site Number : 8260015

🇬🇧

London, United Kingdom

Investigational Site Number : 8260012

🇬🇧

Southampton, United Kingdom

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