Triastek D23 (Budesonide Ileum Targeted Tablets) Receives Positive Clinical Results
The D23 clinical study was randomized, open-label, single-dose, 2-sequence, 4-period, fully repeated crossover trial design. Using an innovative method labeled D23 tablet components and observing in vivo tablet GI transit via X-ray imaging, the study examined the time-course of D23 GI transit and corresponding budesonide pharmacokinetics.
The X-ray imaging results demonstrated that budesonide from D23 tablets is not released until the tablets reach the ileum providing maximum budesonide exposure at the desired site of action. Since the site of disease origin is in the ileum, this targeted delivery is hypothesized to optimize budesonide effects on the immune response and treat IgAN at the site of disease origin. The budesonide pharmacokinetic (PK) profile after D23 administration was correlated with the X-ray results, corresponding to budesonide delivery at the ileum in a consistent and predictable manner.
Following on these positive results, D23 is advancing to the next phase of clinical trials to evaluate the clinical effectiveness of targeted delivery of budesonide with IgAN patients via D23 printed tablets.
The MED® 3D printing process and 3D microstructure designs allow for precise control of the release behavior of drugs in the body by the choice of delay layer material, layer thickness and the resulting composition to degrees not previously possible, in contrast to traditional tableting techniques utilizing a delay layer and drug core. In addition to creating a delay, the subsequent drug release can also be accomplished in various manners, including immediate, sustained and pulsed release.
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Contact
Triastek
Public Relation
Jiaxin Tao
taojiaxin@triastek.com
This news is a press release provided by Triastek, Inc..