-

Triastek D23 (Budesonide Ileum Targeted Tablets) Receives Positive Clinical Results

NANJING, China--(BUSINESS WIRE)--Triastek announces that its 3D printed drug product D23 (Budesonide Ileum Targeted Tablets for the treatment of IgAN) has achieved positive results in recent clinical study. D23 is budesonide delayed-release tablet made by 3D printing using Melt Extrusion Deposition (MED®) process first developed in scale by Triastek based on its proprietary 3D Microstructure for Intestine Targeting (3DμS®-IT) platform. This proprietary platform allows for precise intestinal targeting of drug release and delivery ensuring that the budesonide reaches the ileal area of the intestine where the disease originates and budesonide would be most beneficial. It is anticipated that this targeted delivery will provide significant advantages in the treatment of patients with IgAN disease over current therapies.

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.

Contacts

Public Relation, Jiaxin Tao, taojiaxin@triastek.com

More News From Triastek

Triastek's 3D-Printed Gastric Retention Product T20G Receives FDA IND Clearance

NANJING, China--(BUSINESS WIRE)--Today, Triastek announces that on February 27, 2025 a proprietary 3D-printed non-vitamin K antagonist oral anticoagulant (NOAC) product, T20G, received Investigational New Drug (IND) clearance from the U.S. Food and Drug Administration (FDA). This regulatory milestone follows the prior IND clearance of this product by China's National Medical Products Administration (NMPA) in January 2024. Atrial fibrillation (AF), the most common type of treated heart arrhythmi...

Triastek Announces Research Collaboration and Platform Technology License Agreement with BioNTech to Advance 3D Printed Oral RNA Therapeutics

NANJING, China--(BUSINESS WIRE)--Triastek Inc. ("Triastek"), a global leader in 3D printing pharmaceuticals, today announced that it has entered into a research collaboration and platform technology license agreement with BioNTech SE ("BioNTech"), a next generation immunotherapy company pioneering novel therapies for cancer and other serious diseases. Under the agreement, the companies will develop RNA therapeutics for oral delivery based on 3D printing technology. The collaboration aims to pro...

MED™ 3D Printed Pharmaceutical Product Receives IND Clearance From the US FDA

NANJING, China--(BUSINESS WIRE)--Triastek, Inc. (“Triastek”), a pharmaceutical company specializing in 3D printing of drug products, announced today that the United States Food and Drug Administration (FDA) has approved its Investigational New Drug (IND) 505(b)(2) application for its first 3D printed drug product – T19, indicated for the treatment of rheumatoid arthritis (RA). Developed in-house, Triastek has global intellectual property rights to the T19 3D printed formulation. The novel desig...
Back to Newsroom