New formulations and methods of use of tiropride

By introducing an alkaline agent and enteric coating into telolide formulations, the gastric side effects and pharmacokinetic issues of existing formulations have been resolved, resulting in faster drug absorption and higher bioavailability, and improved patient compliance.

CN122374013APending Publication Date: 2026-07-10BIOPROJET PHARMA
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
BIOPROJET PHARMA
Filing Date
2024-10-15
Publication Date
2026-07-10

AI Technical Summary

Technical Problem

Existing telolide formulations have problems such as severe gastrointestinal side effects, poor patient compliance, and poor pharmacokinetics when used to treat excessive daytime sleepiness and cataplexy.

Method used

The teloridine formulation, which includes an alkaline reagent and an enteric coating, optimizes pharmacokinetics through the alkaline reagent and reduces gastric side effects by utilizing the enteric coating, thereby improving patient compliance.

Benefits of technology

It achieves faster time to peak drug absorption (Tmax), larger area under the curve (AUC), and higher bioavailability, while reducing gastric side effects and improving patient compliance.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present application relates generally to dosage forms (e.g., oral dosage forms) and pharmaceutical compositions comprising a pharmaceutically active agent comprising telotristat or a pharmaceutically acceptable salt, solvate, or hydrate thereof; a basic agent; a delayed release coating; and optionally one or more pharmaceutically acceptable excipients; and to methods of using the dosage forms and pharmaceutical compositions, and methods of making the dosage forms and pharmaceutical compositions.
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Citation Information

Patent Citations

  • Enteric coated stable oral pharmaceutical composition of acid unstable drug and process for preparing the same

    US20040028737A1

  • Method for producing coated pharmaceuticals and food supplements with concentration gradients in the coating thereof

    US20050271778A1

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