ELISA-based Diagnostics of Hereditary Kidney DiseasesPatentedCE / IVDR

A reliable, simple diagnostic solution for hereditary kidney disease ADTKD (Autosomal Dominant Tubulo-Interstitial Kidney Disease). Utilizing a specially developed ELISA-based method to detect the MUC1 protein in blood plasma, this cost-effective technique allows for comprehensive screening and monitoring of disease progression and therapy efficiency. Optimized for large-scale testing, this method provides an accessible alternative to expensive genetic testing and aims to be certified and marketed under a license-based collboration for a global use. 

Pipeline

Product / technology
(target/biomarker)
Discovery stageDevelopmentScale-upCommercializationCommercial partner
Proof-of-conceptPre-clinic dataClinical validationCE / IVDRMarket
Kidney Diagnostics
(ELISA/MUC1 Biomarker)
Progress: 70 %Immunotech

Project details

ELISA-Based method for detection of MUC1 protein in biological samples

GeneSpector presents a solution for a reliable and simple diagnosis of hereditary kidney disease ADTKD (Autosomal Dominant Tubulo-Interstitial Kidney Disease).

Tens of millions of people in the USA and EU alone have genetic predispositions to kidney diseases. Without a timely and proper treatment, diseases such as ADTKD can lead to a gradual kidney failure, requiring dialysis and even a transplant. Currently, diagnosis of such disorders requires expensive and complicated genetic testing that cannot be used for comprehensive and preventive screening.

Presented solution utilizes a specifically developed ELISA-based method for detection of form of MUC1 protein—which causes kidney failure in ADTKD patients—in blood plasma. The ELISA technique is time-proven, doesn’t require any complicated instrumentation, and can be performed even in makeshift conditions. Therefore, it can be used as a first, inexpensive step in complex nephrology diagnostics.

Unlike genetic testing, the ELISA-based method can monitor plasmatic levels of MUC1 protein in real-time. Therefore, it allows monitoring of disease progression as well as efficiency of an applied therapy.

The method is fully developed and optimized for large-scale testing.

Contact

GeneSpector s.r.o.
Petrska 1180/3 110 00 Prague, Czech Republic
ID No / IČO: 09404546, file number C 335854
administered by the Municipal Court in Prague

General queries,
investors & partners

info@genespector.com

 

US subsidiary

GeneSpector Innovations USA, Inc.
3500 South Dupont Highway
Dover DE 19901

EU subsidiary

GeneSpector s.r.o.
Petrska 1180/3
110 00 Prague, Czech Republic
ID No / IČO: 09404546
File number C 335854
administered by
the Municipal Court in Prague