Retail treats every clinical-trial readout as a lottery ticket. We matched 1,752 phase readouts to real stock returns (2022-2026) to see what actually happens. Facts, not advice.
Most readouts are duds, but not as many as you’d be told.
The median readout moved the stock 3.8%, and 56.5% landed within ±5%. That is the headline. The tails are what matter: 7.6% crashed 30%+ and 3.1% ran 50%+. A readout is not a coin flip; it is a mostly-nothing event with a fat, ugly left tail.
Cumulative % move from the pre-readout close through the next trading day. Every figure carries its sample size.
1. The distribution
How far did the stock move?
Share of readouts
Within ±2%: a genuine non-event
35.1%
Within ±5%
56.5%
Within ±10%
70.8%
Crashed 30% or more
7.6%
Ran 50% or more
3.1%
A note on honesty. Our own internal tiering calls 68% of these readouts “FLAT”, and it would have been an easy, punchy stat to publish. We didn’t, because that bucket spans −14.9% to +5.0%; it is asymmetric, and a 14% decline is not “nothing.” The honest number is 56.5% within ±5%. If a statistic needs a generous bucket to sound impressive, it isn’t the statistic.
This is corroborated by the peer-reviewed literature.
A published event study in PLOS One (“The reaction of sponsor stock prices to clinical trial outcomes”) finds median cumulative abnormal returns of roughly +0.8% for positive events and −2.0% for negative: i.e. the median readout barely moves the stock. Our retail-scale finding lands in the same place. We are not claiming a discovery; we are putting a well-established academic result in front of the people who need it.
2. The same event is a non-event for a large-cap and a coin-flip for a micro
Cap tier
n
Median |move|
Within ±5% (a dud)
Crashed 30%+
Micro
350
8.71%
32%
11.7%
Small
424
6.16%
45%
10.8%
Mid
543
2.99%
63%
5.3%
Large
435
1.67%
79%
3.9%
For a large-cap, 79% of readouts are duds and only 3.9% crash. For a micro-cap, just 32% are quiet and 11.7% crash 30%+: a 3× higher wipe-out rate. Same catalyst class, completely different risk.
3. Is there a run-up into a readout? No.
Window
n
Median
25th pct
75th pct
D-30 โ D-1
1748
-0.07%
-7.69%
+8.64%
D-10 โ D-1
1750
+0.00%
-4.22%
+4.55%
D-5 โ D-1
1751
+0.23%
-2.12%
+2.84%
Three independent catalyst types. The same answer.
Over 4,834 events across three catalyst classes that share almost nothing, different regulators, different information, different timelines, and all three land within half a percent of zero. No systematic pre-catalyst run-up. The “buy the run-up” folklore that dominates biotech retail is not visible in the data. Individual names run; the population does not.
Corrected 2026-07-13. We previously printed the PDUFA cell as +0.57% (n=1,792). That figure was computed on a panel containing 202 duplicate rows. Deduplicated, it is +0.43% (n=1,661). The conference row was also rebuilt on a wider sampling frame we have since reverted (see the conference study corrections). Neither change alters the conclusion, all three classes still land within half a percent of zero, but we print what the data says, not what we said last week.
We could find no published study of pre-announcement drift for biotech catalysts: the event-study literature concentrates on announcement-day returns. We state that as a gap we could not fill by searching, not as a claim to be first.
Method
Universe. 1,752 clinical-trial readouts by US-listed biotechs, 2022-2026, matched to daily closing prices. Measure. The cumulative % move from the last close before the readout through the first trading day after; readouts are frequently released outside market hours, so a same-day-only measure would miss most of the reaction. Run-up. Trading-day windows to the last pre-readout close. Statistics. Median and interquartile range; we do not report a mean (a handful of 500%+ moves would dominate it) and we never report a “win rate.”
Caveats.
1. Outcome labels are not used here. This page measures price reaction, not whether a trial succeeded. We deliberately do not publish trial success rates from our own labels; 65% of our readouts are unlabelled, and a rate computed on the labelled subset would be biased. For phase success probabilities, cite Wong, Siah & Lo (2019) and BIO/Informa, who measure it properly.
2. Selection. Our universe is readouts we track, weighted toward companies where the readout was material enough to disclose.
3. Dispersion, not prediction. Nothing here forecasts any individual trial. The distribution is wide, and the left tail is the part that ends companies.
Cite this dataset. CC BY 4.0. “pdufa.bio, Biotech stock reaction to clinical trial readouts (2022-2026), n=1,752, https://www.pdufa.bio/research/readout-reaction”
Not affiliated with or endorsed by the FDA. pdufa.bio is an independent publication with no affiliation with, endorsement by, sponsorship by, or connection to the U.S. Food and Drug Administration or any other government agency. “FDA”, “PDUFA” and all company, drug and ticker names are used descriptively and remain the property of their respective owners.
Informational and educational purposes only. Not investment advice. Nothing on this page is investment, legal, tax or medical advice, or an offer or solicitation to buy or sell any security. pdufa.bio is not a registered investment adviser or broker-dealer and does not recommend trades or publish individual-drug approval probabilities. Verify every date and outcome against primary FDA, SEC or company filings. Data is provided as is, without warranty of any kind, and past behaviour does not predict future outcomes.