FDA Awards Jaguar Health $240,000 Grant
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 02 2026
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Jaguar Health received notice from the U.S. Food and Drug Administration's Center for Veterinary Medicine on January 1 that the company has been awarded a $240,000 grant. Canalevia-CA1 is currently conditionally approved for chemotherapy-induced diarrhea in dogs. The grant will support Jaguar's ongoing study for the treatment of CID in dogs.
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Analyst Views on JAGX
About JAGX
Jaguar Health, Inc. is a commercial stage pharmaceuticals company. The Company is developing prescription medicines sustainably derived from plants from rainforest areas for people and animals with gastrointestinal distress, specifically associated with overactive bowel, which includes symptoms such as chronic debilitating diarrhea, urgency, bowel incontinence, and cramping pain. Its marketed drug Mytesi, (crofelemer 125 mg delayed-release tablets), is a first-in-class oral botanical drug product approved by the FDA for the symptomatic relief of noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy. Its Canalevia-CA1, crofelemer delayed-release tablets drug, is an oral plant-based prescription product that is FDA conditionally approved to treat chemotherapy-induced diarrhea in dogs. It has an exclusive distribution agreement for the sale of Gelclair. It is developing a pipeline of prescription drug product candidates to address unmet needs in gastrointestinal health.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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Jaguar Health Subsidiary Napo Signs $18 Million Licensing Deal
- Licensing Agreement Signed: Jaguar Health's subsidiary Napo Pharmaceuticals has entered into a licensing agreement with Woodward Specialty, granting exclusive, non-transferable, royalty-free rights to commercialize Mytesi and Canalevia in the U.S., with an upfront payment of $18 million, including $16 million at signing and $2 million contingent on specific conditions within six months.
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- Buyback Option: The agreement includes a buyback option allowing Napo to reacquire all licensed rights five years after the effective date, contingent upon FDA approval for new Mytesi indications, providing strategic flexibility for future operations.
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