Velocity 2: An Anthrax Vaccine and Antibiotics Clinical Study

Completed · Phase 2

Conditions studied: Anthrax

In brief

This study is designed to evaluate the pharmacokinetic (PK) profiles of ciprofloxacin or doxycycline when administered orally, prior to, and following, the intramuscular (IM) administration of a two-dose schedule of AV7909 administered two weeks apart.

Key facts

Study ID

NCT04067011

Run by

Emergent BioSolutions

People needed

210

Starts

2019-08-12

Expected to finish

2020-03-19

Last updated by the study team

2025-09-08

Who can join

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

You may qualify if…

• Written informed consent obtained from the participant (dated, signed, and captured in the medical chart at the site).
• A male or female, aged 18 to 45 years of age, inclusive, at the time of informed consent.
• Healthy condition as established by medical history and clinical examination before entering into the study.
• Body mass index (BMI) less than or equal to 35.0 kg/m\^2 at the Screening visit.
• Have adequate venous access for phlebotomies.
• For a woman of childbearing potential (WOCBP), negative pregnancy test at Screening and pre-randomization on Day 1, not currently breastfeeding, and no intention to become pregnant during the study period through 12 months after last receipt of any investigational product (IP). Every female participant is considered to be a WOCBP unless she is surgically sterile (hysterectomy, bilateral salpingectomy or bilateral oophorectomy) OR postmenopausal (defined as >12 consecutive months without menses and screen follicle-stimulating hormone > 30 mIU/mL). Women who are not of childbearing potential are allowed to enroll if they are surgically sterile or postmenopausal as defined above.
• Female participants randomized to Groups 1 or 2 must be willing to add a double-barrier method, IUD, or abstinence as back-up forms of birth control since ciprofloxacin and doxycycline may decrease the effectiveness of birth control pills, implantable or injectable contraceptives.

You may not qualify if…

• A Screening clinical laboratory test result greater than the central laboratory's upper limit of normal (ULN) for aspartate aminotransferase (AST), alanine aminotransferase (ALT), random glucose, total bilirubin, blood urea nitrogen (BUN), or creatinine. Other serum chemistry parameters that are not within the reference range will not be considered exclusionary unless deemed clinically significant by the principal investigator.
• History of allergic reaction or intolerance to quinolone antimicrobials or any medical condition that would contraindicate the use of ciprofloxacin, including and not limited to vascular disorders, tendon disorders, certain genetic connective tissue disorders (e.g., Marfan and Ehlers-Danlos syndrome), prolongation of QT interval, seizures, peripheral neuropathy, increased risk of C. difficile infection.
• History of allergic reaction or intolerance to tetracycline antibiotics or any medical condition that would contraindicate the use of doxycycline including an increased risk of C. difficile infection, increases in BUN or an increased sensitivity to direct sunlight or ultraviolet radiation resulting in erythema.
• Has a need for any of the prohibited medications or requires the medications/foods within the prohibited times.
• Have a tattoo/scar/birthmark or any other skin condition affecting the deltoid area that may interfere with injection site assessments.
• History of anthrax disease, suspected exposure to anthrax, or previous vaccination with any anthrax vaccine.
• Have previously served in the military any time after 1990 or plan to enlist in the military any time from Screening through the final telephone contact.
• Previous anaphylactic reaction, severe systemic response, or serious hypersensitivity to a prior immunization or a known allergy to synthetic ODNs, aluminum, formaldehyde, benzethonium chloride (phemerol).
• Plan to have an elective surgery at any point during the study until after the final safety phone contact.
• Have donated or plan to donate blood within one month prior to enrollment or at any point during the study until after the final safety phone contact.
• Use of any investigational or non-registered product (drug, vaccine or biologic) within 30 days preceding the dose of study vaccine, or planned use during the study until after the final safety phone contact.
• Planned administration of any commercially-available vaccine from one week prior to the first study vaccination through two weeks after the last vaccination.
• Have experienced chronic dosing (defined as more than 14 days) with any immune-modifying drugs within six months of study enrollment. This includes oral, intramuscular, intra-articular, intravenous, or inhalation corticosteroids except in the case of inhaled or intranasal medications for seasonal allergies.
• Receipt of immunoglobulins and/or any blood products within the three months preceding study enrollment or at any point during the study period until after the final safety visit on Day 51.
• An abnormal electrocardiogram (ECG) at screening interpreted as 'Abnormal, Significant'. Inclusion of participants with 'Abnormal, Insignificant' ECGs will be based on the principal investigator's discretion.
• Have an active malignancy or history of metastatic or hematologic malignancy.
• Have a history of an autoimmune, inflammatory, vasculitic or rheumaticor rheumatic disease including but not limited to systemic lupus erythematosus, Guillain-Barré syndrome, myasthenia gravis, polymyalgia rheumatica, diabetes mellitus type I, rheumatoid arthritis or scleroderma.
• A positive laboratory evidence of hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) HIV-1 or HIV-2 infection.
• Positive result on urine drug screen, any evidence of ongoing drug abuse or dependence (including alcohol), or recent history (over the past five years) of treatment for alcohol or drug abuse.
• Has an acute disease at the time of enrollment.
• Any medical condition that, in the opinion of the investigator, could adversely impact the participant's involvement or the conduct of the study.
• Have a significant chronic condition, e.g., serious cardiovascular, pulmonary, hepatic, type II diabetes mellitus or renal disease that, in the opinion of the investigator, would render treatment unsafe or would interfere with trial evaluations or completion of the study.
• An opinion of the investigator that it would be unwise to allow the participant to be randomized into the study.
• Member or immediate family member of an investigator site team.

Where it is running

• Avail Clinical Research, LLC — DeLand, Florida, United States
• The Center for Pharmaceutical Research — Kansas City, Missouri, United States
• Meridian Clinical Research, LLC — Omaha, Nebraska, United States
• New Orleans Center for Clinical Research / Volunteer Research Group — Knoxville, Tennessee, United States

Full record on ClinicalTrials.gov

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