iCeutica


Developer of a proprietary fine-particle platform that reduces drug particle size to submicron dimensions to improve oral bioavailability, reduce pharmacokinetic variability and enable reformulation of marketed and development-stage drugs. Provides formulation development, analytical methods, prototyping and scale-up services and pursues partnered licensing and internal product development in pain/inflammation, oncology and respiratory disease.

Industries

biotechnology
health-care
pharmaceutical

Nr. of Employees

small (1-50)

iCeutica


Products

Pipeline of product candidates using submicron particle technology

Proprietary and partnered candidates across pain & inflammation, oncology and respiratory disease developed using submicron particle formulation approaches to improve PK and clinical performance.


Services

Formulation and prototyping of oral and inhaled products using submicron particle technology.

Analytical support and method development to characterize formulations and support PK/bioavailability studies.

Preparation of clinical trial material from concept through to dosing forms for Phase 1–3 studies.

Scale-up of manufacturing processes and support for commercialization and partner licensing.

Expertise Areas

  • Particle engineering and submicron formulation
  • Formulation development for oral and inhaled dosage forms
  • Clinical trial design and execution for reformulated drugs
  • Pharmacokinetics and bioavailability optimization
  • Show More (4)

Key Technologies

  • Dry milling for particle size reduction
  • Submicron particle-based drug delivery
  • Oral solid dosage formulation (tablet and capsule prototyping)
  • Inhalation formulation engineering
  • Show More (3)

News & Updates

U.S. patent (No. 8,808,751) awarded covering a dry-milling method for producing submicron-sized drug particles.

Partnered reformulations using the submicron particle platform received FDA approvals and U.S. market launches (partner approvals documented in 2013–2014 announcements).

Announcement of a second FDA approval for a partner product developed using the submicron particle platform.


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