Downtrend on the daily chart: below its 50- and 200-day averages · 50-day below the 200-day · SuperTrend down since Sep 28 · below the Ichimoku cloud · RSI 45 · MACD above its signal
None of the 29 investors followed here reported a position in JAGX 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 JAGX 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
| Date | Insider | Transaction | Shares | Value |
|---|---|---|---|---|
| Dec 10, 2025 | Bochnowski James J.Director | — | 6.4K | — |
| Dec 10, 2025 | Micek John J IiiDirector | — | 7.4K | — |
| Dec 10, 2025 | King Steven R. Ph.D.Officer | — | 11.7K | — |
| Dec 10, 2025 | Conte Lisa A.Chief Executive Officer | — | 28.6K | — |
| Dec 10, 2025 | Siegel Jonathan BDirector | — | 7.4K | — |
| Dec 10, 2025 | Lizak Carol R.Chief Financial Officer | — | 11.7K | — |
| Dec 10, 2025 | Wolin Jonathan SGeneral Counsel | — | 11.7K | — |
| Dec 10, 2025 | Jayasuriya AnulaDirector | — | 5.9K | — |
| Dec 10, 2025 | Chaturvedi Pravin ROfficer | — | 11.7K | — |
| May 15, 2025 | King Steven R. Ph.D.Officer | — | 1 | — |
| May 15, 2025 | Conte Lisa A.Chief Executive Officer | — | 2 | — |
| Oct 7, 2024 | King Steven R. Ph.D.Officer | — | 4.9K | — |
| Oct 7, 2024 | Conte Lisa A.Chief Executive Officer | — | 16.5K | — |
| Oct 7, 2024 | Lizak Carol R.Chief Financial Officer | — | 4.3K | — |
| Oct 7, 2024 | Wolin Jonathan SGeneral Counsel | — | 4.9K | — |
| Oct 7, 2024 | Chaturvedi Pravin ROfficer | — | 4.9K | — |
| Year | Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec | Year |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2026 | -27.5 | 31.6 | -58.2 | -46.4 | -49.0 | -15.5 | -66.7 | -20.9 | -62.1 | -7.6 | −99.1% | ||
| 2025 | -12.5 | -30.2 | -69.1 | 157.1 | -64.1 | -42.7 | -19.0 | -20.1 | 42.9 | -16.7 | -30.4 | -31.0 | −96.3% |
| 2024 | -31.1 | -43.3 | 52.5 | 138.9 | -67.3 | -15.2 | -65.6 | -7.3 | 18.4 | -22.2 | -1.0 | -2.9 | −88.9% |
| 2023 | -30.6 | -57.6 | -67.3 | -20.5 | 33.1 | -22.3 | 25.8 | -40.7 | -32.5 | 33.1 | 2.3 | -57.3 | −97.7% |
| 2022 | -21.7 | -44.0 | 55.5 | -36.8 | -18.8 | -19.2 | -12.6 | -8.6 | -33.6 | -10.3 | -7.1 | -33.1 | −91.6% |
| 2021 | 246.0 | -25.5 | -14.3 | -16.1 | 6.0 | -1.2 | -11.4 | -14.3 | -36.9 | -6.2 | -38.5 | -20.6 | −57.5% |
| 2020 | -4.1 | -25.8 | -15.8 | -5.0 | 5.9 | 0.4 | 34.8 | -38.8 | -27.5 | -31.4 | 75.9 | 132.9 | +1.7% |
| 2019 | 11.4 | -32.2 | 61.8 | -18.2 | -27.9 | -59.3 | -63.4 | -32.6 | 12.9 | -43.5 | -17.6 | 31.3 | −95.0% |
| 2018 | -9.3 | 16.5 | 31.8 | -11.8 | -22.1 | -29.4 | -28.2 | -17.5 | 2.7 | -50.1 | 4.2 | -49.1 | −89.1% |
| 2017 | 15.9 | 43.4 | -16.0 | -14.4 | -22.9 | -19.7 | 5.7 | -33.4 | -46.4 | -9.0 | -14.3 | -10.3 | −80.4% |
| 2016 | 37.8 | -44.2 | -8.7 | 7.6 | -17.6 | 31.4 | -5.4 | -25.3 | -1.5 | -26.6 | -28.6 | 6.7 | −68.2% |
| 2015 | -28.4 | -26.1 | -19.4 | 12.9 | 13.6 | -40.5 | 2.7 | −66.6% |
No analyst coverage for this instrument.
Jaguar Health, Inc., a commercial-stage pharmaceuticals company, focuses on developing plant-based prescription medicines for people and animals with gastrointestinal distress. It operates through two segments, Animal Health and Human Health. The company focuses on developing and commercializing prescription and non-prescription products for companion and production animals; and human products. Its lead prescription drug is Mytesi, an anti-secretory antidiarrheal drug for the symptomatic relief of non-infectious diarrhea in adults with HIV/AIDS on antiretroviral therapy; and Canalevia-CA1, a prescription drug product for chemotherapy-induced diarrhea in dogs. It is also developing Crofelemer, an anti-secretory antidiarrheal drug, which is in Phase III clinical trial for prophylaxis of diarrhea in adult cancer patients; Phase II clinical trials for rare/orphan disease indications, including short bowel syndrome with intestinal failure and microvillus inclusion disease; diarrhea-predominant irritable bowel syndrome; and for idiopathic/functional diarrhea. In addition, the company is developing Mytesi which is in Phase III clinical trial for cancer therapy-related diarrhea, as well as Phase II clinical trial for irritable bowel syndrome; and NP-300, a second-generation antidiarrheal drug that is in Phase I clinical trial for symptomatic relief and treatment of moderate-to-severe diarrhea. The company is headquartered in San Francisco, California.