Provista receives AZ Innovative Award from Governor Janet Napolitano
Provista Featured on Channel 12 News
Provista Featured on Channel 5 News
|
Provista on the News
Provista (PLS), was established in 2006
as a medical diagnostics commercialization organization to oversee the
operations of three technology companies as well as a laboratory services
company. Each technology company, Biomarker Technologies,
RCP Diagnostics, and GW Medical Technologies, offers novel
blood diagnostic technologies that have the potential for a
large impact on the healthcare diagnostics market.
BT Test™
- The BT Test is designed to detect the presence of breast cancer at the molecular
level unlike mammography, which only detects masses or gross changes in
breast tissue via x-ray imaging.
-
The BT Test is an IP protected blood test that
offers women a more comfortable test method and greater convenience while
providing caregivers higher sensitivity, early detection capabilities, broader range
of age applicability and ease of administration.
-
The test measures five key
cancer-associated biomarkers and when combined and adjusted for age, has
shown the potential to detect early stage breast cancer.
RCP-Dx Test™
- The RCP Test is a new diagnostic that screens for these four
cancers from a single blood sample. The patented RCP Test is designed
to identify distinctive protein patterns in the blood that reflect the
presence of four estrogen-related cancers.
-
The RCP Test is both highly sensitive and highly specific to this protein, called Riboflavin Carrier Protein (RCP). An accurate screening test for women’s cancers is an essential tool, especially for women in their twenties and thirties for whom mammography has little diagnostic value.
-
The RCP Test has demonstrated the ability to detect early and staged
breast cancer at better than 92%, more accurate than any other
diagnostic on the market today.
LymPro Test®:
- The LymPro Test® is a diagnostic blood test that is 95%
accurate and can assist in the early detection and therapeutic
intervention of AD when currently approved drugs are most effective.
- Developed and clinically evaluated by the University of Leipzig,
a major European medical research university, the Lymphocyte
Proliferation Test (LymPro Test) uses two biomarkers to quantify AD.
In an initial study evaluation, the LymPro Test demonstrated both a
high correlation with clinical AD diagnosis and the potential to
diagnose the disease before the appearance of its clinical symptoms.
MEDIA/INVESTOR CONTACT: Julie Johnson, Communications Manager,
602-468-0067 or johnsonj@provistals.com
Copyright © 2006 Provista
|