Assays / Prenatal and congenital infections
Prenatal and congenital infections
ToRCH Multiplex Antibody Panel
A pipeline candidate that uses the platform’s multiplex design to screen for several congenital infections from one prenatal sample.
At a glance
Targets
Toxoplasma gondii, rubella, cytomegalovirus (CMV) and herpes simplex virus (HSV)
Sample
Serum, plasma or whole blood
Readout
Separate result per target (planned)
Status
Future pipeline
Why it matters
Clinical context
Infections with toxoplasma, rubella, CMV or herpes during pregnancy can harm the baby. Antibody testing helps clinicians understand immunity and possible recent infection, and results are usually interpreted together with the full clinical picture and follow-up testing.
How OncoFirm will measure it
Built on the OncoFirm fluorescent platform
Several answers from one sample
The multiplex strip architecture planned for other panels is designed to carry the ToRCH targets side by side.
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.
Related assays
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.