A Study to Assess the Safety, Pharmacodynamics, and Immunogenicity of PXVX0047

Emergent BioSolutions

Status and phase

Terminated

Phase 1

Conditions

Adenoviral Infection

Treatments

Biological: PXVX0047 Vaccine

Biological: Teva Ad4/Ad7 Vaccine

Study type

Interventional

Funder types

Industry

Other U.S. Federal agency

Identifiers

NCT03160339

PXVX-AD-047-001

Details and patient eligibility

About

PXVX0047 (Adenovirus Type 4 and Type 7 Vaccine [A549 Cells], Live, Oral) is an investigational vaccine in development for the indication of active immunization against adenovirus infection. The primary goals of this Phase 1 study are to evaluate safety, pharmacodynamics (viral shedding), and immunogenicity of PXVX0047.

Enrollment

25 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Male or female
Age 18 to 35
Seronegative for Ad4 and Ad7 by CPE-based assay
(if female of childbearing potential) Using an acceptable method of contraception
If male, subject agrees to use a highly effective method of contraception with female sexual partners of childbearing potential
Able and willing to provide informed consent for study participation

Exclusion criteria

Current acute febrile illness
Current acute gastrointestinal illness
Clinically significant cardiac, respiratory, or gastrointestinal disease
(if female of childbearing potential) Pregnant or nursing, or who plan to become pregnant or nurse during the study
Persons with occupations which may create an increased risk of transmission of vaccine virus (including but not limited to health care workers, child or elderly care providers, food handlers or preparers) who also have expected occupational contact with children less than 7 years of age, pregnant or nursing women, women of childbearing potential not using an acceptable method of contraception, or chronically ill or immunosuppressed individuals through Day 29.
Expected household contact with children less than 7 years of age, pregnant or nursing women, women of childbearing potential not using an acceptable method of contraception, or chronically ill or immunosuppressed individuals through Day 29.
Laboratory evidence of infection with Hepatitis B/C or HIV.
History of severe allergic reaction (e.g. anaphylaxis) to any component of the vaccine.
Inability to swallow capsules or tablets whole without chewing or crushing.
Immunosuppressed individuals, including those treated or planned to be treated with systemic immunosuppressive medications within the 30 days prior to enrollment through 30 days after study treatment.
Concomitant or planned use of other vaccines, investigational agents, cidofovir, ribavirin, or medications expected by the Investigator to have antiviral activity against adenovirus within 30 days prior to enrollment through Day 29.
Any other condition that, in the opinion of the Investigator, creates an unacceptable risk to the subject.
Any other condition that, in the opinion of the Investigator, may interfere with the conduct of the study or the validity of the data.