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Cancer Vaccine

mRNA Vaccines for Lyme Disease

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
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Summary

This trial is testing two different vaccines for Lyme disease in healthy adults. One vaccine targets seven parts of the bacteria, and the other targets just one. The vaccines use mRNA to teach the immune system to recognize and fight the bacteria.

Who is the study for?
Adults aged 18-70 with a BMI of 18-39 kg/m2 can join this Lyme disease vaccine trial. Women must not be pregnant, use reliable contraception, or abstain from pregnancy-causing activities. Excluded are those who've had recent immunosuppressants, immune therapies, Lyme treatment/vaccination, tick bites within 4 weeks, skin conditions affecting assessments, or severe vaccine reactions.
What is being tested?
The study is testing the safety and body's response to two experimental vaccines against Lyme disease: heptavalent mRNA-1975 and monovalent mRNA-1982 compared to a placebo. Participants will receive injections and their health responses will be monitored.
What are the potential side effects?
Potential side effects may include typical vaccine reactions such as soreness at the injection site, fatigue, headache or fever. More serious allergic reactions like anaphylaxis could occur but are rare.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Trial Design

8Treatment groups
Experimental Treatment
Placebo Group
Group I: mRNA-1982: Dose 3Experimental Treatment1 Intervention
Participants will receive 3 IM injections of the mRNA-1982 vaccine at Dose level 3 on Days 1, 57, and 169.
Group II: mRNA-1982: Dose 2Experimental Treatment1 Intervention
Participants will receive 3 IM injections of the mRNA-1982 vaccine at Dose Level 2 on Days 1, 57, and 169.
Group III: mRNA-1982: Dose 1Experimental Treatment1 Intervention
Participants will receive 3 IM injections of the mRNA-1982 vaccine at Dose Level 1 on Days 1, 57, and 169.
Group IV: mRNA-1975: Dose 4Experimental Treatment1 Intervention
Participants will receive 3 IM injections of the mRNA-1975 vaccine at Dose level 4 on Days 1, 57, and 169.
Group V: mRNA-1975: Dose 3Experimental Treatment1 Intervention
Participants will receive 3 IM injections of the mRNA-1975 vaccine at Dose Level 3 on Days 1, 57, and 169.
Group VI: mRNA-1975: Dose 2Experimental Treatment1 Intervention
Participants will receive 3 IM injections of the mRNA-1975 vaccine at Dose level 2 on Days 1, 57, and 169.
Group VII: mRNA-1975: Dose 1Experimental Treatment1 Intervention
Participants will receive 3 intramuscular (IM) injections of the mRNA-1975 vaccine at Dose Level 1 on Days 1, 57, and 169.
Group VIII: PlaceboPlacebo Group1 Intervention
Participants will receive 3 IM injections of vaccine-matching placebo on Days 1, 57, and 169.

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
The most common treatments for Lyme Disease include antibiotics and emerging mRNA vaccines. Antibiotics work by directly targeting and preventing the replication of Borrelia burgdorferi bacteria, aiding the immune system in clearing the infection. Emerging mRNA vaccines, such as mRNA-1975 and mRNA-1982, introduce messenger RNA sequences that instruct cells to produce proteins mimicking parts of the bacteria, triggering an immune response. This helps the body recognize and fight the bacteria if exposed in the future. Understanding these mechanisms is crucial for Lyme Disease patients as it emphasizes the importance of both immediate bacterial eradication and long-term immune preparedness.
Inflammatory myopathy occurring shortly after severe acute respiratory syndrome coronavirus 2 vaccination: two case reports.Vaccination with Messenger RNA: A Promising Alternative to DNA Vaccination.mRNA vaccines - a new era in vaccinology.

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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
111 Previous Clinical Trials
61,380,157 Total Patients Enrolled

Media Library

mRNA-1975 (Cancer Vaccine) Clinical Trial Eligibility Overview. Trial Name: NCT05975099 — Phase 1 & 2
Lyme Disease Research Study Groups: mRNA-1975: Dose 1, mRNA-1975: Dose 3, mRNA-1975: Dose 2, mRNA-1982: Dose 2, mRNA-1982: Dose 3, mRNA-1975: Dose 4, mRNA-1982: Dose 1, Placebo
Lyme Disease Clinical Trial 2023: mRNA-1975 Highlights & Side Effects. Trial Name: NCT05975099 — Phase 1 & 2
mRNA-1975 (Cancer Vaccine) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05975099 — Phase 1 & 2
~443 spots leftby Mar 2026