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Trial record 2 of 6 for:    moderna | rsv

A Study to Evaluate the Safety and Efficacy of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in Adults ≥60 Years of Age

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ClinicalTrials.gov Identifier: NCT05127434
Recruitment Status : Recruiting
First Posted : November 19, 2021
Last Update Posted : January 31, 2023
Sponsor:
Information provided by (Responsible Party):
ModernaTX, Inc.

Brief Summary:
The main purpose of this study is to evaluate the safety and tolerability of mRNA-1345 vaccine and to demonstrate the efficacy of a single dose of mRNA-1345 vaccine in the prevention of a first episode of RSV-associated lower respiratory tract disease (RSV-LRTD) as compared with placebo from 14 days postinjection through 12 months.

Condition or disease Intervention/treatment Phase
Respiratory Syncytial Virus Drug: Placebo Drug: mRNA-1345 Phase 2 Phase 3

Detailed Description:

The study will be conducted in 2 phases: Phase 2 and Phase 3. In the Phase 2 segment, up to 2,000 participants will be randomly assigned to receive a single injection of either mRNA-1345 vaccine at the selected dose or placebo in a 1:1 randomization ratio.

In the Phase 3 segment, approximately 35,000 participants will be randomly assigned to receive a single injection of either mRNA-1345 vaccine at the selected dose or placebo in a 1:1 randomization ratio.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 37000 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: A Phase 2/3, Randomized, Observer-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of mRNA-1345, an mRNA Vaccine Targeting Respiratory Syncytial Virus (RSV), in Adults ≥60 Years of Age
Actual Study Start Date : November 17, 2021
Estimated Primary Completion Date : December 31, 2023
Estimated Study Completion Date : November 30, 2024

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: mRNA-1345
Single injection of mRNA-1345 on Day 1.
Drug: mRNA-1345
Sterile liquid for injection

Experimental: Placebo
Single injection of mRNA-1345 matching-placebo on Day 1.
Drug: Placebo
0.9% sodium chloride (normal saline) injection




Primary Outcome Measures :
  1. Number of Participants with Solicited Local and Systemic Adverse Reactions (ARs) up to 7 Days Postinjection [ Time Frame: Up to 7 days postinjection ]
  2. Number of Participants with Unsolicited Adverse Events (AEs) up to 28 Days Postinjection [ Time Frame: Up to 28 days postinjection ]
  3. Number of Participants With Medically Attended AEs (MAAEs), Adverse Events of Special Interests (AESIs), Serious Adverse Events (SAEs), and AEs Leading to Withdrawal up to 24 Months Postinjection [ Time Frame: Up to 24 months postinjection ]
  4. Vaccine Efficacy (VE) of mRNA-1345 to Prevent a First Episode of RSV-LRTD with 2 or More Symptoms within the Period of 14 Days Postinjection up to 12 Months Postinjection [ Time Frame: 14 days postinjection up to 12 months postinjection ]
    VE of mRNA-1345 to prevent reverse transcription polymerase chain reaction (RT-PCR) confirmed protocol-defined RSV-LRTD, defined as 100*(1-HR ratio), where HR is the hazard ratio (mRNA-1345 versus placebo).

  5. VE of mRNA-1345 to Prevent a First Episode of RSV-LRTD with 3 or More Symptoms within the Period of 14 Days Postinjection up to 12 Months Postinjection [ Time Frame: 14 days postinjection up to 12 months postinjection ]
    VE of mRNA-1345 to prevent reverse transcription polymerase chain reaction (RT-PCR) confirmed protocol-defined RSV-LRTD, defined as 100*(1-HR ratio), where HR is the hazard ratio (mRNA-1345 versus placebo).


Secondary Outcome Measures :
  1. VE of mRNA-1345 to Prevent a First Episode of RSV-Associated Acute Respiratory Disease (RSV-ARD) within the Period of 14 Days Postinjection up to 12 Months Postinjection [ Time Frame: 14 days postinjection up to 12 months postinjection ]
    VE of mRNA-1345 to prevent RT-PCR confirmed protocol-defined RSV-ARD, defined as 100*(1-HR ratio), where HR is the hazard ratio (mRNA-1345 versus placebo).

  2. VE of mRNA-1345 to Prevent First Hospitalization Associated with RSV-ARD or RSV-LRTD within the Period of 14 Days Postinjection up to 12 Months Postinjection [ Time Frame: 14 days postinjection up to 12 months postinjection ]
    VE of mRNA-1345 to prevent first hospitalization associated with RSV-ARD or RSV-LRTD, defined as 100*(1-HR ratio), where HR is the hazard ratio (mRNA-1345 versus placebo).

  3. Geometric Mean Titer (GMT) of Serum RSV Neutralizing Antibodies (Abs) [ Time Frame: Baseline through up to 24 months postinjection ]
  4. Geometric Mean Concentration (GMC) of Serum RSV Binding Abs [ Time Frame: Baseline through up to 24 months postinjection ]
  5. Seroresponse Rate in RSV Neutralizing Abs [ Time Frame: Baseline through up to 24 months postinjection ]
  6. Geometric Mean Fold-Rise of Postbaseline/Baseline Ab Titers [ Time Frame: Baseline through up to 24 months postinjection ]
  7. Proportion of Participants with ≥4-fold Increases in Ab Titers from Baseline [ Time Frame: Baseline through up to 24 months postinjection ]


Information from the National Library of Medicine

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Ages Eligible for Study:   60 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Key Inclusion Criteria:

  • Adults ≥ 60 years of age who are primarily responsible for self-care and activities of daily living. Participants may have one or more chronic medical diagnoses (including chronic heart failure [CHF] and chronic obstructive pulmonary disease [COPD]), but should be medically stable
  • Body mass index from ≥18 kilograms (kg)/square meter (m^2) to ≤35 kg/m^2

Key Exclusion Criteria:

  • Participation in another clinical research study where participant has received an investigational product (drug/biologic/device) within 6 months before the planned date of the Day 1 study injection.
  • Current participation in research involving receipt of any investigational RSV product
  • History of a serious reaction to any prior vaccination or Guillain-Barré syndrome within 6 weeks of any prior influenza immunization.
  • Received or plans to receive any non-study vaccine within 28 days before or after the Day 1 study injection.

Other inclusion and/or exclusion criteria may apply.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05127434


Contacts
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Contact: Moderna Clinical Trials Support Center 1-877-777-7187 clinicaltrials@modernatx.com

Locations
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Sponsors and Collaborators
ModernaTX, Inc.
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Responsible Party: ModernaTX, Inc.
ClinicalTrials.gov Identifier: NCT05127434    
Other Study ID Numbers: mRNA-1345-P301
First Posted: November 19, 2021    Key Record Dates
Last Update Posted: January 31, 2023
Last Verified: January 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by ModernaTX, Inc.:
Viral Diseases
Messenger RNA
Moderna
mRNA-1345
Respiratory syncytial virus
Safety
Vaccines
Additional relevant MeSH terms:
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Virus Diseases
Infections