Assays / Sexually transmitted infections

Sexually transmitted infections

HSV-1/HSV-2 Type-Specific Antibody Assay

A pipeline candidate for type-specific herpes simplex serology on the OncoFirm reader.

Future pipeline

At a glance

Targets

Type-specific antibodies to HSV-1 and HSV-2

Sample

Serum, plasma or whole blood

Readout

Instrument-read (planned)

Status

Future pipeline

Why it matters

Clinical context

Herpes simplex infections are very common and often unrecognized. Current guidelines favor type-specific IgG antibody tests over IgM tests, because IgM results do not reliably show whether an infection is new. Future OncoFirm development will follow that guidance.

How OncoFirm will measure it

Built on the OncoFirm fluorescent platform

Guideline-aligned design

Development is planned around type-specific IgG targets rather than the IgM format described on earlier versions of this page.

A strip that checks itself

Every strip carries a fluorescent reference line of known brightness. Reading the test line against it corrects for reader and temperature drift, and the reader flags runs that did not flow correctly.

A traceable digital record

Each result is stored with the date, operator and lot, ready to share with a clinic record or laboratory system instead of being retyped by hand.

Where it's headed

Development roadmap

This assay is a candidate for the OncoFirm pipeline. Timing depends on partnerships and funding; the stages below show the path it will follow once prioritized.

01

Feasibility

Antibody pairs, fluorescent conjugates and strip layout are selected and tested against the target.

02

Assay development

Strip, reagents and reader settings are optimized, and pilot lots are built.

03

Analytical validation

Precision, linearity, interference and lot-to-lot consistency are measured against reference methods.

04

Clinical evaluation and launch

Performance is evaluated with clinical samples. First release is planned for research use only, followed by regulatory submissions.

Development status. This assay and the OncoFirm platform are in development. They have not been cleared or approved by the FDA and are not available for sale. First products are planned for research use only. Descriptions reflect design goals, not demonstrated performance.

Partner on this assay

We welcome research, clinical, manufacturing and distribution partners. Tell us how this assay fits your work.