"President Trump is facing an impossible landscape created by years of regulatory neglect. We built a federally compliant, pharmaceutical grade marijuana medicine to bring order to that chaos. MMJ offers the President a path that respects the law, protects patients, and restores integrity to cannabinoid science."
-Duane Boise, President & CEO, MMJ International Holdings
Jaguar's requesting advice from EMA on EU approval pathway for general diarrhea of FDA conditionally approved Canalevia®
A novel non-antibiotic approach to diarrhea treatment is important because there are no FDA-approved drugs to treat general diarrhea in dogs, the second most common reason for visits to veterinary emergency hospitals
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- New Composition of Matter Intellectual Property ("IP") Filing Centered on First-in-Class, Fully Synthetically Manufactured Halneuron®-
- New Synthetic Process to be Used for Phase 3 Development Provides Higher Manufacturing Yields and Reduces Costs Versus Naturally Harvested Halneuron® -
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New Industry Aims to Create U.S. Manufacturing Jobs While Supporting Colombian Farmers Transitioning to Legal, High-Value Hemp Production
Read MoreCompany plans to distribute Dream Bowl 2026 Meme Coin to shareholders as of a to-be-determined December 2025 date with distribution expected in January 2026
PSA is a validated FDA-recognized clinical endpoint in assessing prostate cancer treatment response; Telomir-1 lowered PSA levels in a dose-related manner.
Read More"Subsidiaries deliver strong revenue performance as MDCE advances development of innovative AI-driven health and nutrition technologies."
Read MoreThis new IP supports crofelemer's global exclusivity in rare pediatric intestinal failure coincident with published clinical data showing reductions in parenteral support requirements with crofelemer - supporting Jaguar's strategy to secure non-dilutive partnership funding
Recent publication by members of Jaguar's Scientific Advisory Board and other intestinal failure key opinion leaders: "Targeted Literature Review and Assessment of Evidence in Microvillus Inclusion Disease (MVID)"
Read MoreConformity with stringent new EU regulations for medical devices confirmed
Allows for commercialization of Bentrio in EU member states; facilitates regulatory approval in various other countries
Major milestone in international growth strategy
Crofelemer can potentially extend lives of MVID patients - infants and children who face the lethal natural history of the disease
Parenteral support reduction of up to 37% is groundbreaking; No approved treatments exist for MVID in any region
Read MoreNon-dilutive financing from premier lender bolsters strong balance sheet and provides increased flexibility
Company reiterates 2025 financial guidance provided on 3Q25 earnings call and targets cash breakeven by 2028
Read MoreAnnounces three-year business strategy and commercial growth drivers, targeting up to 10% revenue growth in 2026
Expects to expand seasonal vaccine franchise from three to up to six approved products by 2028
Targets readouts from nine ongoing Phase 2 and Phase 3 clinical studies in its oncology pipeline, including three Phase 3 programs for intismeran autogene
Further improves 2026 and 2027 expected GAAP operating expenses by approximately $0.5 billion each year on path to targeted cash breakeven in 2028
Read MoreNew capabilities strengthen U.S. production, completing Moderna's domestic end-to-end mRNA manufacturing network
More than $140 million investment will create hundreds of highly skilled biomanufacturing jobs
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With the global pain-management market projected to surpass $93.9 billion by 2030 and topical analgesics growing at a 7.2% CAGR, CBDL positions itself for major East Coast expansion amid surging consumer demand for natural relief solutions.
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