Have I got this right?28 Jul 2021 09:59
I'm trying to work out how this works.
"ANGLE has been selected to develop immunofluorescence (IF) assays using its Parsortix® system to detect two specific protein markers expressed by circulating tumour cells (CTCs) and implicated in DNA damage repair (DDR), an increasing area of focus for oncology drug development. ...
...As part of the contract, ANGLE will develop the two assays to detect the target proteins in four hard-to-treat cancers: triple negative breast cancer, prostate cancer (including metastatic and/or castration resistant), ovarian cancer (including high grade) and pancreatic cancer."
The assays detect the 2 proteins involved in DNA damage repair, which therefore show the presence of cancer. But also may be part of some kind of drug treatment system.
Then, "The clinical trial phase will incorporate longitudinal analysis of patient samples (for example before, during and after treatment with the investigational drug) and is expected to generate further significant revenues for ANGLE. " So a drug is being trialled for which these assays show ongoing effectiveness, probably at short intervals through the treatment period. That's how they assess the effectiveness of the drug - or not.
Should the drug be effective in the long run it would be in use for a huge number of difficult cancers: breast, prostrate, ovarian and pancreatic, as above. One would hope that as normal treatment progressed effectiveness in each patient would be assessed ongoing, probably using Angle's assay, which would mean Angle would be involved in the regular treatment of a huge number of patients.
Should the drug not be effective the assay will be available to Angle, not the commissioning unnamed company, for any other prospective treatments aimed at these proteins.
Sounds good to me.