From bench to bioequivalence: in vitro mechanistic understanding of ASD drug products in simulated gastrointestinal conditions

Active Cooperative Agreement Awarded Last action

Award ID
U01FD008388
Recipient
Awarding agency
Obligated
$498,970

Award facts

Assistance listing
93.103 Food and Drug Administration Research
Completion date 72% complete
Funding agency
Center for Drug Evaluation and Research Food and Drug Administration, Department of Health and Human Services
Place of performance
Research Triangle Park, Durham, NC, USA

Award details come from USAspending.gov.

Description

Abstract
The findings from this project will enhance our comprehension of how food and gastric PH affects the release of drugs from asds, and how the variability arising from differences in formulations and manufacturing can impact upon in vivo performance. This project will generate tiny-timsg data on a series of amorphous solid dispersion (ASD) drug products under fasted; FED and reduced gastric PH conditions and correlate this in vitro data to in vivo clinical data. In the second step, a mechanistic modeling-based methodology will be employed to link the in vitro dissolution obtained in the tiny-timsg system to the in vivo performance of ASD drug products. Using this in silico model, clinical performances of ASD formulation variants will be simulated, and virtual be (VBE) conducted to assess the impact of formulation and manufacturing process modification on API's exposure. The series of ASD drug products will be carefully selected to ensure that there is diversity in products based on: method of manufacture; excipient composition and the ratio of stabilizing polymer:API. Access to clinical data is critical in the selection of products hence the initial focus will be on the identification of relevant data sets. All products to be tested will be interrogated to identify data on degree of solubility enhancement required; PH dependent solubility and reported food effect. Where formulations are not commercially available they will be manufactured to match reported parameters using dissolution matching as the primary target. Output data from the tiny-timsg will report the ratio of bioaccessible dose in either the FED or the reduced gastric PH state to the fasted state; this will be correlated to the clinical data of the ratio of the AUC in the FED or the reduced gastric PH state to the fasted state. Each formulation's performance in the tiny-timsg will be closely interrogated to identify the kinetics of precipitation to mechanistically understand ASD performance. The closely controlled and reproducible nature of tiny-timsg will enable discrimination at a level not possible with pre- clinical or clinical testing; hence the ability to discriminate between formulations and identify risks associated with food or reduced gastric PH in the prediction of in vivo outcomes. Coupling the tiny-timsg data to pbpk models will support formulation development and minimize future clinical testing thus accelerating the speed of development of safe and effective medicines. The developed and validated workflow will help to establish scientific and regulatory standards for supporting innovative development of asds and performing virtual bioequivalence evaluation of these generic drug products.

Transactions

Action Obligated Date
Amendment $249,485
Original award $249,485

Quick answers

Who received award U01FD008388?

U01FD008388 was awarded to Simulations Plus Inc. by FDA Office of Acquisition and Grant Services (Food and Drug Administration) on September 1, 2024.

How much is award U01FD008388 worth?

$498,970 has been obligated on U01FD008388.

Which agency awarded U01FD008388?

FDA Office of Acquisition and Grant Services (Food and Drug Administration) awarded U01FD008388, with funding from Center for Drug Evaluation and Research (Food and Drug Administration).

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