Uptrend on the daily chart: above its 50- and 200-day averages · 50-day above the 200-day · SuperTrend down since Oct 7 · above the Ichimoku cloud · RSI 57 · MACD above its signal
None of the 29 investors followed here reported a position in PXMD in their latest filing.
From each investor's quarterly 13F filing with the SEC: positions at the quarter's end, reported up to 45 days later. All investors
No member of Congress has disclosed a PXMD trade since 2025.
From House and Senate STOCK Act reports. Members disclose trades, not holdings, as value ranges up to 45 days later, so amounts are estimates and “last move” is a hint at who still holds it, not a position. All recent congress trades
No insider transactions reported for PXMD.
| Year | Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec | Year |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2026 | 300.0 | 50.0 | 16.7 | -28.6 | 40.0 | -28.6 | 40.0 | 0.0 | -28.6 | 40.0 | +600.0% | ||
| 2025 | -49.8 | -99.7 | 100.0 | -50.0 | 0.0 | 0.0 | 0.0 | 100.0 | -50.0 | 4900.0 | -98.0 | 0.0 | −99.8% |
| 2024 | -31.8 | 22.1 | -19.0 | 46.1 | -55.7 | -34.1 | 10.3 | -10.4 | -48.8 | -2.5 | -11.4 | -35.1 | −91.8% |
| 2023 | 33.0 | -23.0 | -8.2 | -20.4 | -11.8 | -41.3 | -19.6 | -28.8 | -36.4 | -35.2 | -70.8 | -17.7 | −97.8% |
| 2022 | -18.9 | -12.5 | 14.3 | -15.4 | −31.4% |
No analyst coverage for this instrument.
PaxMedica, Inc., a clinical stage biopharmaceutical company, focuses on the development of anti-purinergic drug therapies for the treatment of disorders with intractable neurologic symptoms. Its lead product candidate is PAX-101 that is in Phase 3 clinical trials, an intravenous formulation of suramin for the treatment of autism spectrum disorder, myalgic encephalomyelitis/chronic fatigue syndrome, long COVID-19 syndrome, fragile X syndrome, human African trypanosomiasis (HAT), and fragile X-associated tremor/ataxia syndrome. The company is developing PAX-102, an intranasal formulation of suramin for neurologic indications, as well as other new chemical entities that are targeted and selective antagonists of purine receptor subtypes; and PAX-HAT-301 for the treatment of HAT. It has a research collaboration agreement with PolarMar Health for Phase II clinical trial in austism spectrum disorder for emodin, which retains the rights for PolarMar to develop and commercialize any non-prescription supplement form of the product, and for PaxMedica, Inc. to retain exclusive rights to develop and commercialize a highly purified form of emodin. The company was formerly known as Purinix Pharmaceuticals LLC and changed its name to PaxMedica, Inc. in April 2020. PaxMedica, Inc. was incorporated in 2018 and is based in Tarrytown, New York.
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