Study to Demonstrate Consistency of Three Lots of a Live-attenuated Chikungunya Virus Vaccine Candidate in Healthy Adults

Completed · Phase 3

Conditions studied: Chikungunya Virus Infection

In brief

This was a prospective, randomized, double-blinded, multicenter Phase 3 clinical study investigating three Lots of VLA1553 at the final dose. Overall 409 healthy subjects aged 18 to 45 years were randomized into the study.

Key facts

Study ID

NCT04786444

Run by

Valneva Austria GmbH

People needed

409

Starts

2021-02-22

Expected to finish

2022-01-26

Last updated by the study team

2023-09-28

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18 to 45 years of age on the Day of screening
• Able to provide informed consent
• Generally healthy as determined by the Investigator's clinical judgement based on medical history, physical examination and screening laboratory tests
• For women of childbearing potential:
• practiced an adequate method of contraception during 30 days before screening
• negative serum or urine pregnancy test at screening or vaccination, respectively
• agreed to employ adequate birth control measures for the first three months post-vaccination.

You may not qualify if…

• CHIKV infection in the past (self-reported), including suspected CHIKV infection; was taking medication or other treatment for unresolved symptoms attributed to a previous CHIKV infection; or had participated in a clinical study involving an investigational CHIKV vaccine
• Acute or recent infection (and not symptom-free in the week prior to screening)
• Tested positive for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV);
• Received another live virus vaccine within 28 days or inactivated vaccine within 14 days prior to vaccination in this study or plans to receive a vaccine within 28 days or 14 days after vaccination, respectively
• Abnormal findings in any required study investigations (including medical history, physical examination, and clinical laboratory) considered clinically relevant by the Investigator which pose a risk for participation in the study
• Medical history of or currently had acute or progressive, unstable or uncontrolled clinical conditions that posed a risk for participation in the study
• History of immune-mediated or clinically relevant arthritis / arthralgia
• History of malignancy in the past 5 years other than squamous cell or basal cell skin cancer. If there had been surgical excision or treatment more than 5 years ago that was considered to have achieved a cure, the subject could be enrolled.
• Known or suspected defect of the immune system, such as subjects with congenital or acquired immunodeficiency, including infection with HIV, status post organ transplantation or immuno-suppressive therapy within 4 weeks prior to vaccination.
• History of any vaccine related contraindicating event (e.g., anaphylaxis, allergy to components of the candidate vaccine, other known contraindications)
• Clinical conditions representing a contraindication to intramuscular vaccination and blood draws
• Pregnant, had plans to become pregnant during the first three months post-vaccination or lactating at the time of enrollment
• Donation of blood, blood fractions or plasma within 30 days or received blood-derived products (e.g. plasma) within 90 days prior to vaccination in this study or planned to donate blood or use blood products until Day 180 of the study
• Rash, dermatological condition or tattoos that would, in the opinion of the Investigator, interfere with injection site reaction rating
• Known or suspected problem with alcohol or drug abuse as determined by the Investigator
• Any condition that, in the opinion of the Investigator, could compromise the subjects well-being, could interfere with evaluation of study endpoints, or could limit the subject's ability to complete the study;
• Committed to an institution (by virtue of an order issued either by the judicial or the administrative authorities)
• Participation in another clinical study involving an investigational medicinal product (IMP) or device within 30 days prior to study enrollment or is scheduled to participate in another clinical study involving an IMP, or device during the course of this study
• Member of the team conducting the study or in a dependent relationship with one of the study team members. Dependent relationships include close relatives (i.e., children, partner/spouse, siblings, parents) as well as employees of the Investigator or site personnel conducting the study.

Where it is running

• AMR Miami — Coral Gables, Florida, United States
• AMR Fort Myers — Fort Myers, Florida, United States
• St. Johns Center for Clinical Research — Ponte Vedra, Florida, United States
• AMR Wichita West — Wichita, Kansas, United States
• AMR Lexington — Lexington, Kentucky, United States
• Walter Reed Amy Institute of Research — Silver Spring, Maryland, United States
• Alliance for Multispecialty Research (AMR) — Kansas City, Missouri, United States
• Meridian Clinical Research — Omaha, Nebraska, United States
• Wr-Crcn, Llc — Las Vegas, Nevada, United States
• Rochester Clinical Research — Rochester, New York, United States
• AMR Knoxville — Knoxville, Tennessee, United States
• Dynamed Clinical Research — Tomball, Texas, United States

Full record on ClinicalTrials.gov

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