Evaluation of the SRI B. Anthracis Lethal Factor Diagnostic System

Anthrax Clinical Trial

Official title:

Clinical Specificity Evaluation of the SRI B. Anthracis Lethal Factor Diagnostic System

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT05672875
• Other study ID #: 4650.367
• Status: Terminated
• Start date: January 23, 2023
• Est. completion date: April 20, 2023

Study information

• Verified date: November 2023
• Source: SRI International
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study is intended to estimate the Anthrax LF Dx System specificity. Sensitivity will be estimated with 10% of the samples spiked with recombinant Bacillus anthracis lethal factor (LF) used to prepare contrived positive samples.

Description:

This is a prospective, non-interventional, multi-center study assessing the clinical specificity of the Anthrax LF Dx System using venous blood samples collected from presumptive anthrax negative adult male and female healthy and symptomatic subjects (non- B. anthracis infected). Up to 500 subjects may be enrolled to meet the goal of 440 evaluable subjects (220 healthy and 220 symptomatic). Subjects will have one venous blood sample collected from a single time-point tested with the Anthrax LF Dx System. At each clinical site, specimens will be randomly selected such that 10% (40 of 400) of all subjects' venous blood samples (total of 40 [20 healthy and 20 symptomatic]) will be spiked with recombinant B. anthracis LF to prepare a contrived positive sample. An unblinded operator will prepare the spiked samples and provide both the spiked and neat samples to a blinded operator for testing on the Anthrax LF Dx System. Thus, the blinded operator will receive samples that could either be spiked (positive) or neat (presumed negative) to preserve the blind.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 343
• Est. completion date: April 20, 2023
• Est. primary completion date: April 20, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female subject who is =18 years of age
• Subject is willing and able to provide Informed Consent for study participation, prior to any study mandated procedures
• For the healthy human population: Subject is in general good health with a stable health status based on medical history, and the investigator's clinical judgment

defined as:

• No acute medical conditions that require the use of systemic prescription medications in the last 30 days and
• Any chronic medical diagnoses/conditions should be stable for the last 30 days (no hospitalizations, emergency room (ER), or urgent care for condition). This includes no change in chronic prescription medication, dose, or frequency as a result of deterioration of the chronic medical diagnosis/condition in the 30 days before enrollment.
• For the symptomatic human population:
• Current symptoms consistent with cold, flu or other bronchial and symptomatic infections. The subject must currently (day of consent) have at least one of the following symptoms: fever, chills, chest discomfort, shortness of breath, cough, dizziness/confusion, nausea, headache, sweats, fatigue, or body aches.

Exclusion Criteria:

• Subject has inclusion symptoms and tests positive for COVID-19.
• Subject has previously enrolled in this study, or subject has previously failed screening for this study.
• Subject has any medical or social or psychiatric condition(s) or current substance abuse that, in the opinion of the investigator, would preclude the subject's ability to provide informed consent/assent, or to comply with the study requirements.
• Currently enrolled in an investigational drug or device clinical study in which the primary endpoint has not occurred or occurred within the last 30 days.
• Subject is a nursing home resident.
• Subject is a prisoner.

Related Conditions & MeSH terms

• Anthrax

Intervention

Diagnostic Test:
• Anthrax LF Dx System
Lateral flow immunoassay for the detection of the LF biomarker in whole blood samples.

Locations

Country	Name	City	State
United States	WellNow Urgent Care and Research	Cincinnati	Ohio
United States	WellNow Urgent Care and Research	Columbus	Ohio
United States	WellNow Urgent Care and Research	Dayton	Ohio

Sponsors (2)

Lead Sponsor	Collaborator
SRI International	Department of Health and Human Services

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The estimated negative percent agreement (NPA) of the Anthrax LF Dx System test.	The estimated NPA will be calculated from testing neat specimens from 400 subjects (with presumed negative samples).	Day of enrollment
Primary	Adverse events	All adverse events directly related to specimen collection will be reported.	Within 24 hours of blood draw
Secondary	The estimated percent positive agreement (PPA) of the Anthrax LF Dx System test.	PPA will be estimated with samples spiked with recombinant B. anthracis lethal factor (LF) used to prepare contrived positive samples.	Day of enrollment