Northwest Biotherapeutics’ Annual Shareholder Meeting Key Takeaways
Feb 6th 2019, $NWBO, $0.24, $128M market capitalization
The well-attended Annual Shareholder Meeting (ASM) on Feb 2nd 2019 strengthened my conviction for NWBO. All of the board’s recommendations were approved and there was a sizable turn-out in person or proxy. While I believe that the initiation of analyst coverage could immediately help NWBO realize a more appropriate value as a Phase III clinical asset in the hot immuno-oncology space, the key takeaways from the ASM are focused on fundamental value:
- The company is laser-focused on the series of steps that they identified to get to top-line data, which will be the major value-inflection point.
- I have extreme confidence in their ability to execute the steps
- I get the sense that they have enough capital to execute the steps, particularly with the remaining 17 acres in the UK that can be monetized, if needed.
- The steps are each multi-month processes and there is some overlap where there can be parallel processing. I'm guessing this means 6 months of work, but we are 2-3 months into the work, so I'm guessing top-line data could be available at the end of May. Notably, ASCO is May 31st - June 4th - The company is compelled to unveil at ASCO because it is the main event for revealing clinical oncology advances. On the other hand, some have guessed top-line data will be available at the end of the year. February 12th is the deadline to retain the opportunity to submit an abstract to ASCO 2019.
- They have stated that they are submitting the Statistical Analysis Plan to four distinct geographical/market regions - This gives them four independent chances at regulatory success and four chances at commercialization/revenue. i.e. the probability of regulatory success in at least one of the four markets is better than the probability of regulatory success if they were to submit to only one market.
- If top-line data is compelling, then the valuation could reach $10-20B based on the CAR-T valuations and with the understanding that DCVax represents a platform that can be applied more readily to a larger set of indications (i.e. each CAR-T drug that addresses a new target must go through the drug development process and each first-generation CAR-T prep for each patient requires a genetic engineering step, which is not required for DCVax). To be clear, DCVax is easier to produce than first-generation CAR-Ts.
- I was reminded that their facility has the capacity for 10,000 patients per year, which is large enough to drive it to the valuations cited above.
- The general feel was that the board has greater confidence, optimism, and unity than ever before.
Along with the key takeaways above, I have a growing sense that the company intends to inflict maximum value at the most advantageous moment for shareholders. A crescendo, with a vengeance.
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