PIPELINE


 
The 505(b)(2) NDA pathway streamlines drug development by leveragingexisting safety and efficacy data, reducing timelines, costs, and risks comparedto traditional methods. This approach accelerates market entry, offeringpatients safe, effective, and innovative treatments while addressing unmetneeds like improved dosage forms and tailored solutions for specificpopulations. TAHO leverages this pathway to deliver better therapies, bridgeinnovation with accessibility, and drive progress in healthcare.




 

PRODUCT DEVELOPMENT

First Once Daily Anticoagulant Oral Film for Patients with Dysphagia

Along with TAH3311, TAHO is also developing an extended-release oral film that can treat stroke and systemic embolism caused by NVAF, a condition where the heart beats irregularly. Most of the existing treatments are either pills or injections, which are not suitable for many elderly patients who have trouble swallowing. Moreover, the current apixaban oral tablets need to be taken twice daily, making it hard to switch from other treatments that only require once-daily dosing.

TAHO’s extended oral film is the first of its kind that can deliver apixaban without the need for swallowing. Makes it easier and more convenient for both older and younger NVAF and PE patients. TAHO’s extended-release oral film aims to capture a large share of the global market for novel anticoagulants, which is worth more than $12 billion.

Verification

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