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Veloxis Pharmaceuticals

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Type
  
Public

Website
  
www.veloxis.com

Number of employees
  
30

Key person
  
William J. Polvino M.D.

Industry
  
Pharmaceuticals

Headquarters
  
Denmark

Founded
  
1999

Veloxis Pharmaceuticals wwwveloxiscomimageslogopng

Traded as
  
Nasdaq Copenhagen: VELO

Key people
  
William J. Polvino, M.D. (President and CEO), Kim Bjørnstrup (Chairman)

Products
  
Orally-delivered pharmaceuticals

Stock price
  
VELO (CPH) DKK 1.06 +0.01 (+0.95%)31 Mar, 4:43 PM GMT+2 - Disclaimer

Veloxis Pharmaceuticals A/S, formerly LifeCycle Pharma A/S, develops improved versions of difficult-to-formulate drugs with its proprietary drug formulation technology, called MeltDose®. Veloxis is focused on building a clinical and market-stage pharmaceutical business around its late-stage transplant immunosuppression product candidate LCP-Tacro. The company was founded in 2002 as a spin-off from H. Lundbeck A/S. Veloxis is headquartered in Horsholm, Denmark, with an office in Cary, North Carolina

Contents

MeltDose Technology Platform

MeltDose works by incorporating a drug substance with low water solubility into a "meltable" vehicle. It is then sprayed on an inert particulate carrier using fluid bed equipment.

The melt is solidified when deposed on a particle carrier, and thus captures the active drug in a solid dispersion either as a solid solution or in a nano-crystalline state. The particle size is then increased by controlling and optimizing the product temperature and feed rate of the melt.

The granulate can be directly compressed into tablets without additional processing steps besides blending with a lubricant. In addition, the technology allows for customization of the release profile.

Once in tablet form, the dissolution profile and the particle size of drugs manufactured using MeltDose® technology remain stable allowing for a long shelf-life.

Product Pipeline

  • LCP-Tacro (tacrolimus) is a once-daily dosage version of tacrolimus for prevention of rejection in organ transplant patients in two Phase 3 clinical trials in kidney transplant patients. The first study in stable transplant patients showed that LCP-Tacro was non-inferior in efficacy and safety compared to twice-daily tacrolimus (Prograf®) [ESOT REF]. The second Phase 3 clinical trial in de novo patients is ongoing. A Phase 3b clinical trial evaluating whether patients experiencing symptomatic tremor on twice-daily tacrolimus demonstrate improvement in their tremors when switched to LCP-Tacro is ongoing.
  • FENOGLIDE (fenofibrate) for dyslipidemia, marketed in the U.S. by Santarus, Inc.
  • References

    Veloxis Pharmaceuticals Wikipedia