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Virus Therapy
JCXH-221 Vaccine for COVID-19
Phase 1
Waitlist Available
Research Sponsored by Immorna Biotherapeutics, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age: 18 years of age or older, at screening.
Status: Healthy subjects.
Must not have
Subjects who received convalescent serum or prior therapeutic antibodies against SARS-CoV-2 within 4 months before Day 1.
Subjects with history of myocarditis or pericarditis, or with AEs after mRNA vaccination that are in nature and severity beyond the common AEs expected and necessitating medical intervention.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 1- day 365 (12 months)
Summary
This trial is testing a new vaccine called JCXH-221 in healthy adults aged 18 and older. The vaccine aims to train the immune system to recognize and fight off infections. Researchers are looking to find a safe and effective dose while monitoring the immune response.
Who is the study for?
Healthy adults over 18 who've completed their initial COVID-19 vaccination series at least 4 months prior can join. They shouldn't have had recent exposure to COVID-19, current infections, or past SARS-CoV-2 infection confirmed within the last 4 months. People on COVID-19 treatment meds or with immune system issues are excluded.
What is being tested?
The trial is testing JCXH-221, a new mRNA-based vaccine for broad protection against COVID-19. Phase 1 compares it to a placebo in healthy volunteers, while Phase 2 uses an FDA-approved vaccine as the active comparator to find the best dose and measure immune responses.
What are the potential side effects?
While specific side effects aren't listed here, common reactions to vaccines like soreness at injection site, fatigue, headache, muscle pain may occur. Severe allergic reactions are rare but possible; monitoring for myocarditis or pericarditis will likely be part of safety assessments.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
I am currently healthy without any ongoing medical conditions.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I haven't received COVID-19 convalescent serum or antibodies in the last 4 months.
Select...
I have had severe reactions to mRNA vaccines or have a history of heart inflammation.
Select...
I do not have a fever or signs of an infection at the time of enrollment and vaccination.
Select...
I have an immune system condition.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 1- day 365 (12 months)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 1- day 365 (12 months)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
AE frequency
Injection site reaction
Medical AE frequency
+3 moreSecondary study objectives
SARS-CoV-2 anti-receptor antibody levels
SARS-CoV-2 antibody levels
Other study objectives
T-cell responses
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Investigational productExperimental Treatment1 Intervention
Patients randomized to this arm will be given the investigational product (JCXH-221).
Group II: PlaceboPlacebo Group1 Intervention
Patients randomized to this arm will be given a placebo vaccine.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
JCXH-221
2023
Completed Phase 1
~80
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
Common treatments for infectious diseases often work by either directly targeting the pathogens or by stimulating the immune system to enhance its response. Vaccines like JCXH-221 are designed to stimulate both humoral and cellular immune responses, which involve the production of antibodies and activation of T-cells, respectively.
This dual approach helps the body to recognize and eliminate pathogens more effectively. Antiviral drugs, such as those used for COVID-19, may inhibit viral replication, while antibiotics target bacterial cell walls or protein synthesis.
Immunomodulatory treatments, like monoclonal antibodies, can enhance the immune system's ability to fight infections. These mechanisms are crucial for infectious disease patients as they provide targeted and efficient ways to control and eliminate infections, reducing morbidity and mortality.
South American Hemorrhagic Fevers: A summary for clinicians.Splenic CD8α⁺ dendritic cells undergo rapid programming by cytosolic bacteria and inflammation to induce protective CD8⁺ T-cell memory.
South American Hemorrhagic Fevers: A summary for clinicians.Splenic CD8α⁺ dendritic cells undergo rapid programming by cytosolic bacteria and inflammation to induce protective CD8⁺ T-cell memory.
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
ICON plcIndustry Sponsor
85 Previous Clinical Trials
28,403 Total Patients Enrolled
Immorna Biotherapeutics, Inc.Lead Sponsor
5 Previous Clinical Trials
767 Total Patients Enrolled
Media Library
Research Study Groups:
This trial has the following groups:- Group 1: Investigational product
- Group 2: Placebo
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