Trans-Duodenal Barrier / endoscopically implantable tube prosthesis / revolution in diabetes therapy

for investors

Early Stage Investment.
Opportunity in a fast-growing market.

The Trans-Duodenal Barrier developed by TDC is a patented endoscopic transduodenal bypass implant for combined diabetes/obesity therapy that atraumatically prevents nutrient absorption in the duodenum and delays gastric emptying.

The present prototype has successfully completed initial animal studies (ZIM-funded). Following successful CE certification, commercialization as a class IIb product is expected to start in 2027.

The Trans-Duodenal Barrier is a globally unique product for the pronounced growth market of obesity, DMT2 and NASH (approx. 800 million patients worldwide) and already has a sales potential in the billions at 0.1% penetration.

The uniqueness of the Trans-Duodenal Barrier is based in particular on the patented method of fixation and therefore also allows much broader use than previous methods for combining restrictive and malabsorptive principles of action.

Initial situation

60

million diabetes patients in the EU

26,1

million patients with fatty liver disease

81,3

million obesity patients

Strong upward trend

Treatment methods to date

Conservative therapy

  • Ineffective because usually not effective in the long term
  • “unpopular” because a very high personal contribution is required
  • Medication: not yet successful despite immense investment in research

Surgical therapy

  • Effective, but irreversible
  • Lifelong aftercare, therefore expensive
  • Unclear long-term consequences
  • Fear-inducing

Trans-Duodenal Barrier

1

Implements experience from surgery: Malabsorptive procedures more effective than restrictive procedures alone

2

Simple implantation as part of an outpatient gastroscopy with i.v. sedaton (propofole)

3

No anesthesia, no X-ray fluoroscopy, no medication required

4

Proven efficacy in type 2 diabetes, probable efficacy in fatty liver and obesity

5

Reversible, repeatable, combinable

Roadmap

Q1/2022

Completion of prototype design

Q3/2022

Finalize design

Q2/2024

Start of clinical trial

Q2/2026

Completion of clinical study

Q4/2026

CE certification, preparation for marketing

Q1–2/2027

Start of 3 multicenter PM studies
Development of marketing

Q2/2029

Completion of multicenter PM studies

Please contact us, we will be happy to answer any further questions you may have!