Safety and Immunogenicity Study of a Recombinant Protein Vaccine (NDV-3) Against S.Aureus and Candida

Completed · Phase 1 · Has a placebo group

Conditions studied: Staphylococcal Infections, Candidiasis

In brief

This randomized, double-blind, placebo-controlled study is a first-in-human Phase 1 study using two dose levels of an investigational vaccine directed against S. aureus and Candida. The study is designed to evaluate the safety, tolerability and immunogenicity of the investigational vaccine, NDV-3

Key facts

Study ID

NCT01273922

Run by

NovaDigm Therapeutics, Inc.

People needed

40

Starts

2011-01-01

Expected to finish

2011-12-01

Last updated by the study team

2012-05-22

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Informed of the nature of the study and have agreed to and are able to read, review, and sign the informed consent document prior to screening. The informed consent document will be written in English, therefore the subject must have the ability to read and communicate in English.
• Completed the screening process within 30 days prior to dosing.
• Healthy male and female subjects 18-50 years of age, inclusive, at the time of dosing.
• No clinically significant deviation from normal as judged by the investigator(s) in the medical history, physical examination (including but may not be limited to an evaluation of the cardiovascular, gastrointestinal, respiratory and central nervous systems), vital sign assessments, 12-lead electrocardiogram (ECG), clinical laboratory assessments, and by general observations.
• Female subjects must be:
• of childbearing potential and practicing an acceptable method of birth control described below as judged by the investigator(s); or
• of postmenopausal status (no menses) for at least 1 year and has a documented FSH level ≥ 40 mIU/mL; or
• sterile (surgically [bilateral tubal ligation, bilateral oophorectomy, or hysterectomy] or the Essure® Procedure).

You may not qualify if…

• Reports receiving any investigational drug, investigational vaccine, or investigational device within 30 days prior to dosing.
• Reports any presence or history of a clinically significant disorder involving the cardiovascular, respiratory, renal, gastrointestinal, immunologic, hematologic, endocrine, or neurologic system(s) or psychiatric disease as determined by the clinical investigator(s).
• Clinical laboratory test values outside the accepted range.
• When confirmed upon additional testing, demonstrates a reactive screen for hepatitis B surface antigen, hepatitis C antibody, or HIV antibody.
• Reports a clinically significant illness during the 28 days prior to dosing (as determined by the clinical investigators).
• Demonstrates a positive drug screen for non-prescription drugs.
• Reports a history of allergic response(s) to nickel or anaphylaxis (or other serious reactions) to aluminum.
• Reports receiving any live attenuated vaccine including FluMist® within 6 weeks prior to dosing or any licensed inactivated vaccine within 3 weeks prior to dosing.
• Reports the use of any immunosuppressive drugs, including systemic corticosteroids, within 4 weeks prior to dosing.
• Reports the use of any medications or treatments that may alter immune responses to the study vaccine within 3 weeks prior to dosing (e.g., cyclosporine, tacrolimus, cytotoxic drugs, immune globulin, Bacillus Calmette-Guerin [BCG], monoclonal antibodies, radiation therapy).
• Reports a history of clinically significant allergies including food or drug allergies or anaphylaxis (or other serious reactions) to vaccines.
• Reports a history of drug or alcohol addiction or abuse within the past year.
• Reports receiving any blood products within 3 months prior to dosing and throughout the study.
• Reports donating blood within 28 days prior to dosing. All subjects will be advised not to donate blood for four weeks after completing the study.
• Reports donating plasma (e.g. plasmapheresis) within 14 days prior to dosing. All subjects will be advised not to donate plasma for four weeks after completing the study.
• Reports an intolerance of direct venipuncture.
• Pregnant, lactating, breastfeeding, or intends to become pregnant over the course of the study (females only).
• Demonstrates a positive pregnancy screen (females only).
• Any other medical and/or social (e.g. non-compliant) reason which, in the opinion of the investigator(s), would prevent participation in the study.

Where it is running

• Cetero — Fargo, North Dakota, United States

Full record on ClinicalTrials.gov

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