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Scienture Holdings, Inc. (SCNX) delivers innovative specialty pharmaceuticals and integrated health services within the U.S. healthcare market. This news hub provides investors and industry observers with essential updates on the company's operational developments and strategic initiatives.
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Discover timely updates on strategic partnerships, clinical trial milestones, and healthcare service expansions. The resource maintains strict editorial standards to ensure reliable coverage of financial disclosures and operational developments without speculative commentary.
Bookmark this page for continuous access to Scienture Holdings' official communications and third-party analysis of its Nasdaq-listed performance. Check regularly for updates on initiatives advancing integrated care models and pharmaceutical innovations in specialty markets.
Scienture Holdings (NASDAQ: SCNX) has announced manufacturing and supply chain readiness for Arbli™, their FDA-approved oral liquid losartan suspension (10mg/mL), targeting a commercial launch in July 2025. The company's subsidiary has partnered with Saptalis Pharmaceuticals for manufacturing and secured agreements for warehousing and distribution.
Arbli™ is the first and only FDA-approved ready-to-use oral liquid losartan in the U.S. market, designed for treating hypertension in patients over 6 years old, reducing stroke risk in hypertensive patients with left ventricular hypertrophy, and treating diabetic nephropathy in type 2 diabetes patients. The product holds two USPTO patents pending FDA Orangebook listing.
According to IQVIA data (MAT December 2024), the U.S. losartan market has annual sales of $292 million with 68 million prescriptions. Unlike current market offerings that require compounding from tablets, Arbli™ offers a ready-to-use liquid formulation with reduced dosing volume and room temperature storage stability.
Scienture Holdings (NASDAQ: SCNX) has announced the divestiture of its Healthcare IT and Wholesale Operations subsidiaries - Integra Pharma Solutions, Bonum Health, and Softell - to Tollo Health for $5 million. This strategic move is part of the company's broader realignment to focus exclusively on its Branded and Specialty Pharma segment through Scienture,
The proceeds from the sale will support commercial and strategic product development activities at Scienture, The divestiture aims to achieve three key benefits:
- Increased operational efficiency through streamlined structure
- Cost savings through consolidation of overlapping functions
- Dedicated focus on commercial products and high-value product pipeline
Scienture Holdings (NASDAQ: SCNX) has transformed from a health services IT company to a specialty pharmaceutical company through strategic moves in 2024-2025. The company completed a $22.5M sale of TRXaDE Inc. assets and merged with Scienture Inc. in a $103M all-stock transaction.
The company now has two FDA-approved commercial products scheduled for launch in H2 2025: ArbliTM (in-house developed) and REZENOPY® (acquired in March 2025). The company's pipeline includes multiple products under development:
- SCN-104: Injectable pen for migraine treatment
- SCN-106: CVS therapeutic biosimilar
- SCN-107: Non-opioid post-surgical pain management
REZENOPY®, a 10mg naloxone HCl nasal spray, targets a market with annual sales of $189M. The combined market opportunity for their two commercial products is $481M, based on IQVIA data (December 2024).
SCIENTURE HOLDINGS (NASDAQ: SCNX) has announced two significant developments in its commercial operations. First, Michele Rath has been appointed as Senior Vice President and Chief Commercial Officer (CCO) of Scienture, , effective November 1, 2024. Rath brings over 20 years of industry experience from previous roles at Pfizer, CVS Caremark, and Aurobindo Pharma.
Second, the company has established a strategic partnership with Syneos Health Commercial Services through a Master Commercial Services Agreement (MCSA). Syneos Health will serve as Scienture's Contract Sales Organization, providing field sales, inside sales, and customer engagement services supported by their Kinetic platform analytics.
These developments aim to support the upcoming launches of two FDA-approved products: Arbli™ (losartan potassium) oral suspension and Rezenopy® (naloxone HCl) nasal spray.
Scienture Holdings (NASDAQ: SCNX) has announced a strategic financial move following the FDA approval of Arbli™, their novel liquid losartan formulation. The company has drawn from its Equity Line of Credit (ELOC) to support Arbli's commercial launch while simultaneously suspending further ELOC draws for either 30 trading days or until the stock reaches $10 per share.
Arbli™, the first FDA-approved ready-to-use oral liquid losartan in the U.S. market, is indicated for treating hypertension in patients over 6 years old, reducing stroke risk in hypertensive patients with left ventricular hypertrophy, and treating diabetic nephropathy in certain type 2 diabetes patients. The commercial launch is expected in Q3 2025.
Scienture Holdings (NASDAQ: SCNX) has received FDA approval for ArbliTM (losartan potassium) Oral Suspension, 10 mg/mL, the first and only FDA-approved ready-to-use oral liquid losartan in the U.S. market. The product is indicated for treating hypertension in patients over 6 years old, reducing stroke risk in hypertensive patients with left ventricular hypertrophy, and treating diabetic nephropathy in certain type 2 diabetes patients.
ArbliTM features two USPTO-issued patents and addresses the need for a liquid formulation, eliminating risks associated with crushing tablets. The product offers reduced dosing volume and long-term shelf life at room temperature storage. According to IQVIA data (MAT December 2024), the U.S. losartan market represents approximately $292 million in annual sales with 68 million prescriptions. The company plans to launch ArbliTM in Q3 2025.
Scienture Holdings (NASDAQ: SCNX) has announced a definitive agreement with Summit Biosciences (subsidiary of Kindeva Drug Delivery) for the exclusive U.S. rights to commercially launch REZENOPY®, a 10mg naloxone HCl nasal spray for opioid overdose treatment. The FDA-approved product represents the highest-strength naloxone HCl available in the market.
Under the agreement, Kindeva will manufacture and supply REZENOPY®, while Scienture will own the new drug application (NDA) and handle U.S. sales, marketing, and distribution. The product aims to combat the rising opioid-related fatalities through enhanced potency against powerful opioids.
According to IQVIA data (MAT December 2024), the US naloxone market shows annual sales of $189 million with a unit volume of 10.0 million. The collaboration aligns with Scienture's mission to provide innovative treatment solutions and expand patient access across therapeutic areas.
Scienture Holdings (NASDAQ: SCNX) announced that Dr. Narasimhan Mani, President of Scienture, will participate as an invited speaker and panelist at the 8th Annual Conference of The Society for the Study of Xenobiotics (SSX) in India. The conference is scheduled for January 23-25, 2025, at BITS Pilani, Hyderabad Campus.
Dr. Mani will present on the specialty pharmaceutical industry, focusing on technology-driven product innovations and efficient market strategies for improving patient access to novel therapies. He will also participate in panel discussions about global pharmaceutical industry trends, portfolio development, breakthrough technology platforms, and commercialization strategies.
Scienture Holdings (NASDAQ: SCNX), a specialty pharma company focused on novel brand products, has announced its upcoming participation in The Microcap Conference 2025. The event will be held from January 28-30, 2025, at the Borgata Hotel Spa & Casino in Atlantic City, NJ. The company's management team will present their corporate strategy and conduct one-on-one meetings with institutional and individual investors to discuss recent developments, growth plans, and investment opportunities.
Scienture (NASDAQ: SCNX) announced that the U.S. Patent and Trademark Office has issued a new patent (No. 12,156,869) for its product SCN-102, a Losartan Potassium Oral Suspension. This patent, along with the previously granted patent No. 11,890,273, covers stable liquid pharmaceutical compositions of Losartan and treatment methods. Both patents extend protection through 2041.
The company's SCN-102 product, currently under FDA review, aims to provide a ready-to-use oral liquid formulation of Losartan, one of the most widely prescribed molecules in its class. The patents demonstrate Scienture's development capabilities and commitment to addressing underserved patient needs.
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