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RECRUITING Phase 4

A Study to Evaluate the Immunogenicity and Safety of mRNA-1283 COVID-19 Variant-containing Formulations

NCT07089706 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the immunogenicity and safety of the recommended variant-containing formulations of mRNA-1283 COVID-19 vaccine (mNEXSPIKE®) within the current epidemiological environment.

Conditions Studied

Interventions

  • BIOLOGICAL mRNA-1283.251 Variant-containing Formulation

Study Locations (5)

Louisiana

  • DelRicht Research-Baton Rouge — Baton Rouge
  • DelRicht Research-New Orleans — New Orleans

Georgia

  • DelRicht Research-Atlanta — Atlanta

Mississippi

  • DelRicht Research-Gulfport — Gulfport

Oklahoma

  • DelRicht Research-Tulsa — Tulsa

Trial Details

FieldValue
Enrollment Target 832 participants
Start Date 2025-07-21
Est. Completion 2026-05-11
Phase Phase 4

Sponsor

ModernaTX

67 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07089706

The ClinicalTrials.gov registry entry for NCT07089706 describes a study currently listed as recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 832 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ModernaTX, which has 67 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with COVID-19 appearing as the primary indexed condition, and to 1 intervention — of which mRNA-1283.251 Variant-containing Formulation is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07089706 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Louisiana, Georgia, Mississippi. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07089706 about?

NCT07089706 is a clinical study titled "A Study to Evaluate the Immunogenicity and Safety of mRNA-1283 COVID-19 Variant-containing Formulations". The purpose of this study is to evaluate the immunogenicity and safety of the recommended variant-containing formulations of mRNA-1283 COVID-19 vaccine (mNEXSPIKE®) within the current epidemiological environment.

What is the current status of trial NCT07089706?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 832 participants. The study started on 2025-07-21. Estimated completion is 2026-05-11.

What conditions does trial NCT07089706 study?

This clinical trial studies the following conditions: COVID-19. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07089706?

The interventions under investigation include: mRNA-1283.251 Variant-containing Formulation (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07089706?

This trial is sponsored by ModernaTX, which has 67 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07089706 being conducted?

This trial has 5 study locations across Georgia, Louisiana, Mississippi, Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial