Public market performance of AI-enabled drug developers (a subset of the #TechBio space)
How they've performed (and why they've struggled):
Following several high-profile IPOs, shares of AI-enabled drug developers (AIDD) briefly peaked in Q1'21, before underperforming every quarter thereafter
Collective underperformance of this group:
vs. XBI: (~52%)
vs. NBI (~69%)
vs. S&P (~74%)
What happened?
Given the entire subsector has moved downwards in tandem, we can first look at macro factors:
(1) Generalist and retail investors fled the space: if we use the ARK Genomic Revolution ETF as a proxy for retail sentiment, we see a strong correlation with AIDD performance
A market downturn will cause investors to reduce their risk profile, and thus earlier stage and platform-driven stories will lose favor vs. late-stage, product-driven companies
We saw this de-risking happen across all industries, not just biotech (Source: Atlas Venture)
(2) Rising interest rates: due to being earlier-stage, the majority of value will be realized far in the future
As a result, these names are highly sensitive to rising rates as their future cash flows are discounted to present value at a higher factor
(3) Lack of data-driven catalysts and uncertainty on how to value these relatively unvalidated platforms
These companies went public at huge valuations with preclinical or early clinical programs - as is common in biotech, no news is bad news, so investors turned elsewhere
$RLAY and $SDGR performed better than their peers likely because they were easier to value:
- $RLAY - Solid Ph1. data
- $SDGR - >$150M in rev, high growth DD platform
Of note, drug discovery enablers w/o proprietary programs (i.e. $ABSI, $EVO and $ABCL) led the way down
(4) Jack of all trades, master of none
These companies lack a clear ownership base which introduces long-term stability issues
The engineering / tech-driven approach creates a lot of platform risk for traditional bio funds that prefer first-in-class / best-in-class assets
But, the inherent biological risk, binary clinical trial outcomes and long revenue cycles can deter tech investors
So who should own this as a core portfolio position for the long haul?
With more public biotech co's than ever before to pick from, that can be a tough question
High-conviction anchor investors are critical to provide a low cost of capital for long-term R&D & value creation (Bruce @LifeSciVC has flagged this before)
Below case study of Seagen / Baker Bros illustrates this - BB always stepped up for FOs & when the stock was declining
@LifeSciVC While the space certainly went through a period of being "over-hyped", it would be a mistake to dismiss it altogether
Most platforms, drug programs and companies are too early to draw firm conclusions
Recall Amara's Law tells us to think long-term with new tech
@LifeSciVC Quick plug: If you're interested in learning more about the #TechBio space, consider checking out the Decoding TechBio substack from @patricksmalone, @ameekapadia & the rest of the team
A great weekly summary & balanced perspective on everything happening in the space
My view on the top acquirers for $MDGL after yesterday's stellar data announcement in NASH
+ key late-stage pipeline assets in NASH & catalysts through 2023 & beyond:
I pulled together the initial list above based on big pharma exposure to the NASH / metabolic space and then gave each a score based on these criteria:
(1) Current NASH pipeline (2) Past BD and M&A activity in NASH (3) Mgmt. commentary on M&A preferences (4) Gut feeling
More context on (1): given the emerging belief that combining multiple MoAs is the best way to address the complex pathophysiology of NASH, resmetirom could become a critical combo agent, and thus even companies with their own late-stage pipelines would be interested
I pulled together 44 companies with a range of approaches & segmented assets by development phase
Let's take a deeper look
Keep in mind, this is not the entire cell therapy landscape, but a good snapshot of clinical progress & key assets
With 6 approved products, >$5B in aggregate sales & a shift into earlier treatment lines, cell therapy awareness and adoption has hit a commercial inflection point
Outstanding data and heightened patient awareness have caused demand to outstrip supply, most notably for anti-BCMA CAR-Ts in myeloma
This has amplified the logistical & manufacturing concerns long associated with CAR-T and limited treatment to the specialized hospital setting