Welcome to our dedicated page for Jaguar Health news (Ticker: JAGX), a resource for investors and traders seeking the latest updates and insights on Jaguar Health stock.
Jaguar Health, Inc. (NASDAQ: JAGX) is a commercial-stage pharmaceuticals company specializing in the development of novel prescription medicines sustainably derived from natural plant sources in rainforest areas. The company's primary focus is on addressing gastrointestinal (GI) distress in both humans and animals, with an emphasis on chronic debilitating diarrhea and associated symptoms such as urgency, bowel incontinence, and cramping pain.
Jaguar Health operates through several subsidiaries, including Napo Pharmaceuticals, Inc., which develops and commercializes proprietary human GI pharmaceuticals globally. One of its flagship products, Mytesi® (crofelemer), is FDA-approved for symptomatic relief of noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy. The company’s lead animal prescription drug candidate, Canalevia™, targets forms of diarrhea in dogs, while Equilevia™ supports total gut health in equine athletes.
In addition, Jaguar Health, through its Napo Pharmaceuticals subsidiary, is advancing the development of crofelemer with the ongoing OnTarget study, a pivotal Phase 3 clinical trial aimed at the preventive treatment of chemotherapy-induced overactive bowel (CIOB) in adults with cancer on targeted therapy. Crofelemer has also been designated an Orphan Drug by the FDA and European Medicines Agency for short bowel syndrome (SBS) and microvillus inclusion disease (MVID).
Jaguar Health’s commitment to cancer supportive care is showcased through its preparation to launch Gelclair®, an FDA-approved oral mucositis prescription product, in Q3 2024. This initiative is part of their broader strategy to support cancer patients facing severe treatment side effects.
Beyond GI distress, Jaguar Health has a joint venture called Magdalena Biosciences, in collaboration with Filament Health Corp. This venture focuses on developing plant-based prescription medicines for mental health indications. A recent out-licensing agreement with Magdalena includes a botanical drug candidate for potential schizophrenia and psychoses indications.
Jaguar Health’s financial performance reflects consistent growth, with Q1 2024 revenue at approximately $2.4 million, showing a 20% increase from Q1 2023. Despite operational losses, the company continues to invest in research and development, particularly for rare disease treatments.
For more information, visit Jaguar Health, Napo Pharmaceuticals, Napo Therapeutics, and Magdalena Biosciences. Stay connected with Jaguar Health on LinkedIn, X (formerly Twitter), and Instagram.
Jaguar Health announced on September 21, 2021, that it received confirmation from the FDA's Center for Veterinary Medicine that the Target Animal Safety section of its application for the conditional approval of Canalevia for chemotherapy-induced diarrhea (CID) in dogs is complete. Canalevia, an oral plant-based drug, aims to help dogs undergoing chemotherapy, addressing a significant issue as approximately 40% of treated dogs experience diarrhea that may affect treatment. Launch is expected in December 2021.
Jaguar Health (NASDAQ:JAGX) announced an investor webcast scheduled for September 20, 2021, at 8:30 AM Eastern Time. The company is also launching an educational awareness contest in honor of Indigenous Peoples' Day on October 11, 2021. This fifth contest aims to honor Indigenous healers and will award a winner a book on ethnobotany. Participants must submit answers to multiple-choice questions by 9:00 AM on the contest date. Jaguar Health focuses on developing plant-based pharmaceuticals for gastrointestinal issues.
Jaguar Health (NASDAQ:JAGX) announced that the European Medicines Agency (EMA) has accepted the orphan drug designation application for crofelemer for treating short bowel syndrome with intestinal failure (SBS-IF). This acceptance initiates a formal review process by the EMA's Committee for Orphan Medicinal Products. The company aims to secure conditional marketing authorization in Europe, focusing on this critical orphan disease. Crofelemer, previously designated as an orphan drug by the FDA for SBS in the U.S., has significant market potential, especially given that approximately 10,000 to 20,000 patients may be affected in both the U.S. and Europe.
Jaguar Health (NASDAQ:JAGX) has successfully completed a $776,200 private placement of approximately 309,242 shares of Common Stock. This offering, led by impact investor Josh Mailman and including Jaguar's CEO and CFO, was priced at a premium to market. The company's subsidiary, Napo EU, aims to expand access to its drug crofelemer in Europe, specifically targeting short bowel syndrome. A merger with Dragon SPAC is pending regulatory approval, expected by early October 2021. Ismaila Sougoufara has been promoted to Senior Director, Corporate Controller.
Jaguar Health has appointed Karen J. Brunke, Ph.D., as Executive VP of Corporate and Business Development and Chip Whitlow as Marketing Director. These appointments underscore the company's commitment to advancing crofelemer for treating chemotherapy-induced diarrhea (CID) in dogs, with expected approval in Q4 2021. The appointments aim to foster partnerships for crofelemer's potential human applications and enhance the ongoing commercialization efforts. With an increase in canine cancer diagnoses, these developments signify an important market opportunity for Jaguar.
Jaguar Health, Inc. (NASDAQ:JAGX) announced a 1-for-3 reverse stock split of its common stock, effective September 8, 2021. This decision follows approval from a majority of shareholders at a special meeting held in December 2020. The reverse split aims to align Jaguar's stock price with institutional investing standards, enhancing its appeal to long-term investors. Post-split, every three shares will convert to one, and fractional shares will be compensated with cash. Jaguar continues its focus on developing plant-based non-opioid medicines for gastrointestinal issues.
Jaguar Health, Inc. (NASDAQ:JAGX) announced the voting results from its Annual Meeting of Stockholders held on September 3, 2021. Proposals 1, 2, 4, 5, and 6 were approved, including the election of a director and the ratification of the accounting firm. However, Proposal 3 to increase authorized common stock from 150 million to 290 million shares failed to pass, despite over 75% of votes in favor. The stockholders chose to hold advisory votes on executive compensation every three years. More details are available in the proxy statement filed with the SEC.
Jaguar Health announced its subsidiary, Napo Pharmaceuticals, submitted an abstract for a clinical study on the effects of crofelemer (Mytesi) on the gut microbiome in HIV/AIDS patients for IDWeek 2021.
The study investigates how crofelemer impacts microbiota in people living with HIV/AIDS undergoing antiretroviral therapy. Mytesi is FDA-approved for treating noninfectious diarrhea in these patients. The findings could provide insights into gut health and inflammation related to HIV.
Napo Pharmaceuticals, a subsidiary of Jaguar Health (NASDAQ:JAGX), signed a license agreement with its Italian subsidiary, Napo EU S.p.A., for the development and commercialization of crofelemer and lechlemer in Europe. Napo will receive an upfront payment of $10 million and potential milestone payments. The initial focus is on securing accelerated conditional approval for short bowel syndrome with intestinal failure. Napo EU also plans to explore further indications, contingent on additional payments and funding.
Jaguar Health's subsidiary, Napo Pharmaceuticals, announced the completion of a preclinical toxicology study for lechlemer (NP-300), targeting diarrhea relief from cholera and other infections. Supported by the National Institute of Allergy and Infectious Diseases, this study is crucial for filing an Investigational New Drug (IND) application in early 2022. Lechlemer is derived from Croton lechleri and aims to provide cost-effective treatment, particularly for neglected diseases. The company continues to conduct additional necessary studies for the IND application.
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