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Xceleron Accelerates Early Drug Development

Xceleron combines ultra-sensitive analysis with knowledge of drug ADME/PK in humans. Our clients use this approach in translational medicine and to enable traditional ADME studies with difficult compounds and in sensitive populations.

We have developed a portfolio of services enabling candidate selection and early development decisions before and during clinical Phase I studies and in PII/III.  We conduct Phase 0/Microdosing, intravenous pharmacokinetics, metabolite profiling and mass balance investigations in humans.

Xceleron's clients have access to the world’s most experienced team in this field:

  • Unmatched global analytical capacity
  • Dedicated Quality Assurance professionals
  • Scientists with experience solving drug development problems
  • Tested collaborator network necessary to accelerate pharmaceutical and biotechnology client drug development


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Latest News


12/3/09 Development and Validation of HPLC-AMS Method for Quantification of [14C]-CC-11050 in Human Plasma

11/20/09 Intravenous and Oral Microdose Pharmacokinetics of Three Novel Inhibitors of FabI in Healthy Subjects

10/14/09 Microdose Pharmacokinetics of two NNRTI's published. Idenix's lead compound in-licensed by GSK.

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