A Trial Evaluating the Safety and Effects of an RNA Vaccine ARCT-021 in Healthy Adults
Purpose
This is a Phase 2, randomized, placebo-controlled, and observer-blind study in healthy adults. The study will evaluate the safety, tolerability, and immunogenicity of the SARS-CoV-2 RNA vaccine candidate against COVID-19: As 2 doses (at two different dose levels), separated by 28 days or as 1 dose In adults 18 years of age and older
Conditions
- Covid19
- SARS-CoV Infection
- Corona Virus Infection
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
Individuals who: 1. are able to provide consent 2. agree to comply with all study visits and procedures 3. are willing and able to adhere to study restrictions 4. are sexually active and willing to adhere to contraceptive requirements 5. are male or female ≥18 or (in Singapore) ≥21 years of age 6. are medically stable
Exclusion Criteria
Individuals who: 1. have had SARS-CoV-2 infection or COVID-19 disease. 2. have had cancer except for cancers that were treated and that have low risk of returning 3. have chronic kidney disease 4. have some chronic lung diseases 5. have some heart conditions 6. have compromised immune systems 7. are obese 8. have sickle cell disease or some other blood disorders 9. are current smokers and/or use illegal drugs 10. have Type 2 diabetics 11. are immunocompromised, immunodeficient or have had a transplant 12. have autoimmune disease 13. have other severe or uncontrolled diseases or disease that may interfere with the interpretation of the study 14. have a positive test for hepatitis B or C or human immunodeficiency virus 15. have had a severe reaction to previous investigational vaccines 16. have a fever or are feeling sick close to the time of the first vaccination of the study 17. have positive drug test at screening 18. are pregnant 19. are breastfeeding 20. have a bleeding disorder 21. have previously received an investigational coronavirus vaccine (SARS-CoV(1) or MERS) or who plan to be in other COVID-19 studies 22. have recently been vaccinated with other vaccines 23. have recently received blood products 24. who work at one of the clinic sites participating in this study, work at Arcturus, who work at other companies that monitor the study or close family members to the sites, Arcturus, or partners involved in study monitoring 25. other restrictions may apply
Study Design
- Phase
- Phase 2
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Intervention Model Description
- sequential assignment
- Primary Purpose
- Prevention
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Masking Description
- Observer blind
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Study Group 1, Younger Adult Participants |
Participants will receive one dose of ARCT-021 on Day 0, one dose of Placebo (saline) on Day 28 and on Day 208 either one dose of ARCT-021 or one dose of placebo |
|
|
Experimental Study Group 2, Younger Adult Participants |
Participants will receive one dose of ARCT-021 on Day 0, a second dose of ARCT-021 on Day 28 and on Day 208 either one dose of ARCT-021 or one dose of placebo |
|
|
Experimental Study Group 3, Younger Adult Participants |
Participants will receive one dose of ARCT-021 on Day 0, a second dose of ARCT-021 on Day 28 and on Day 208 either one dose of ARCT-021 or one dose of placebo |
|
|
Placebo Comparator Study Group 4, Younger Adult Participants |
Participants will receive one of Placebo (Saline) on Day 0, one dose of Placebo on Day 28, and one dose of Placebo on Day 208 |
|
|
Experimental Study Group 1, Older Adult Participants |
Participants will receive one dose of ARCT-021 on Day 0, one dose of Placebo (saline) on Day 28 and on Day 208 either one dose of ARCT-021 or one dose of placebo |
|
|
Experimental Study Group 2, Older Adult Participants |
Participants will receive one dose of ARCT-021 on Day 0, a second dose of ARCT-021 on Day 28 and on Day 208 either one dose of ARCT-021 or one dose of placebo |
|
|
Experimental Study Group 3, Older Adult Participants |
Participants will receive one dose of ARCT-021 on Day 0, a second dose of ARCT-021 on Day 28 and on Day 208 either one dose of ARCT-021 or one dose of placebo |
|
|
Placebo Comparator Study Group 4, Older Adult Participants |
Participants will receive one dose of Placebo (saline) on Day 0, a second dose of Placebo on Day 28 and a third dose of Placebo on Day 208 |
|
Recruiting Locations
More Details
- NCT ID
- NCT04668339
- Status
- Terminated
- Sponsor
- Arcturus Therapeutics, Inc.
Detailed Description
This is a multiregional, multicenter, Phase 2, randomized, observer-blind study designed to evaluate the safety, reactogenicity, and immunogenicity of the study vaccine in younger and older adult participants. Enrolled participants will be randomly assigned to receive either study vaccine ARCT-021 or placebo (sterile saline). Approximately 600 participants (300 each in younger [18 to <56 years of age in United States or 21 to <56 years of age in Singapore] and older [≥56 years of age] participants) will be enrolled (including at least 50% of participants in the older cohort ≥65 years of age). Participants will be stratified by age and then randomly assigned (3 ARCT-021:1 placebo) to receive 2 doses of study vaccine separated by 28 days. At 180 days after second study vaccination (Day 208), participants in Study Groups 1, 2, and 3 will be randomly assigned again to receive a single booster dose of study vaccine (randomly assigned as 1 ARCT-021:1 placebo). Study Group 4 will not be randomized but will receive 1 dose of placebo at Day 208. Study Groups are summarized in Table 1. Study vaccine will be administered in an observer-blind fashion. Participants will be followed for safety and immunogenicity through 180 days after booster vaccination (Day 388). At a subset of clinical sites, all enrolled participants will also undergo blood sampling for evaluation of CMI responses. Vaccine doses will be assigned as follows: Younger Age Cohort: Study Group 1: n= 75 participants, ARCT-021 7.5 µg (first dose), Placebo (second dose Study Group 2: n= 75 participants, ARCT-021 5.0 µg (first dose), 5.0 µg (second dose) Study Group 3: n= 75 participants, ARCT-021 7.5 µg (first dose), 7.5 µg (second dose) Study Group 4: n= 75 participants, Placebo (first dose), Placebo (second dose) Booster Vaccine: Study Groups 1, 2, 3: 113 participants, ARCT-021 5.0 µg or 7.5 µg, 112 participants, Placebo Study Group 4: n= 75 participants, Placebo Older Age Cohort: Study Group 1: n= 75 participants, ARCT-021 7.5 µg (first dose), Placebo (second dose Study Group 2: n= 75 participants, ARCT-021 5.0 µg (first dose), 5.0 µg (second dose) Study Group 3: n= 75 participants, ARCT-021 7.5 µg (first dose), 7.5 µg (second dose) Study Group 4: n= 75 participants, Placebo (first dose), Placebo (second dose) Booster Vaccine: Study Groups 1, 2, 3: 113 participants, ARCT-021 5.0 µg or 7.5 µg, 112 participants, Placebo Study Group 4: n= 75 participants, Placebo A DSMB will be in place to independently review the safety data of participants. Pausing Rules are also utilized in this study to reduce risk to study participants. The expected duration of participation for an individual participant is approximately 14 months, inclusive of the Screening period.