Stop metastasis early
Sometimes, metastasis is invisible. Prostate cancer is localized if it cannot be seen (outside the prostate) by the most sensitive imaging technology, PET-CT/PSMA, which can see a 2.3 mm tumor (3 million cells) about 50% of the time.
Metastasis is happening even if it is invisible!
Prostate cancer risk is assessed based on biopsy and MRI.
The number of high risk localized prostate cancer diagnoses per year is about
Develop an antibody drug to treat high risk localized prostate cancer by killing isolated prostate cancer cells.
This makes sense because isolated cancer cells are relatively unprotected, unlike tumors. However we do have to kill small clusters, which migrate in our bodies along with single cancer cells.
Our antibody is actually a cocktail: more than one antibody, because the starting prostate cancer, usually adenocarcinoma, often changes over time into other more dangerous types, including neuroendocrine prostate cancer. We should target such at the start to hinder their proliferation. One protein target is unlikely to suffice to target all species.
No other company is in this space (to our knowledge).
Existing drugs do it for other cells for other diseases. Obinutuzumab kills B cells, for chronic lymphocytic leukemia (annual sales $1.2B). Benralizumab kills eosinophils and basophils, for eosinophilic asthma (annual sales $2.0B). These drugs have very similar design to our drug.
Our antibodies are Fc enhanced for effector function and half life, do not carry payloads, and are not T cell engagers. They are intended for long term use. The antibody targets we choose will all be highly specific.
We are a very early stage (pre-seed) company. Currently we are talking to the prostate cancer community. If you’re curious, we’d love to hear from you — write to us: info@abdabra.com.
David Jaffe is a mathematician turned computational biologist turned antibody developer. Most recently he was a cofounder of Infinimmune, which develops antibody drugs targeted at inflammatory disease. Before that he was Computational Biology Fellow at 10x Genomics; his last project there was to redesign their 10x VDJ platform to do clonotyping correctly; he also built a tool enclone for looking at VDJ data. Before that he was Director of Computational Research and Development in the Genome Sequencing and Analysis Program at the Broad Institute. The work of his group included the development of ARACHNE, ALLPATHS and DISCOVAR. Before that he was Professor of Mathematics at the University of Nebraska – Lincoln, where he worked on algebraic geometry and then error correcting codes. He received his PhD in Mathematics from the University of California – Berkeley. Here are his publications. He entertains himself by running trails with a camera.
photos courtesy DJ
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