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The share price fell to its lowest level since October 2025 today, with an intraday decline of 16.25%.
Pyxis Oncology’s stock has tumbled 23.58% over four consecutive trading days after the release of preliminary Phase I trial data for its ADC candidate, micvotabart pelidotin (MICVO). The therapy showed a 46% confirmed objective response rate in monotherapy and 71% in combination with Keytruda, but 89% of monotherapy patients experienced treatment-related adverse events, with 56% reporting Grade 3 or higher side effects. Investors reacted harshly to the safety profile, sending shares down 49.9% in premarket trading and 45% during the session. CEO Lara Sullivan emphasized MICVO’s “therapeutic potential,” but analysts highlighted the need for clearer risk-benefit balance, particularly as patient discontinuations due to side effects reached 28% in monotherapy trials.

The broader biotech sector saw mixed performance, with some firms benefiting from risk-on sentiment following the FDA’s recent guidance on novel cell therapies, while Pyxis faced renewed skepticism over its ability to manage the safety profile of MICVO. Institutional investors accounted for 72% of today’s volume, with short sellers aggressively building positions as open interest surged to a 6-month high. Retail traders, meanwhile, largely avoided the name, as social media sentiment turned overwhelmingly bearish after a prominent analyst flagged the trial’s high discontinuation rate as a “red flag” for commercial viability.
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