Tranzyme Pharma
Durham, NC
Vipin K. Garg, Ph.D., President & CEO

Company Overview
Tranzyme Pharma is a clinical-stage biopharmaceutical company developing novel small molecule therapeutics for the treatment of gastrointestinal (GI) and metabolic disorders. The Company’s candidate drugs originate from its own discovery pipeline of proprietary compounds and exhibit high affinity for validated and “druggable” targets in the GI tract. Tranzyme is developing first-in-class, mechanism-based therapeutics directed at ghrelin (responsible for upper gut motility, appetite regulation, and energy balance) and motilin (responsible for regulation of GI transit). The Company’s product pipeline includes:

  TZP-101 (Phase I) for acute GI motility disorders such as post-operative ileus. TZP-101 is a ghrelin receptor agonist with potent and selective gastroprokinetic properties that represents the first in its class to enter clinical trials.  
  TZP-102 (late-stage preclinical) a second generation oral ghrelin agonist for chronic and acute instances of gastroparesis, an impairment of GI motility particularly common among diabetics. TZP-102 is on track to enter the clinic by the first quarter of 2007.  
  TZP-201/202 (preclinical) motilin antagonists for diarrhea-predominant irritable bowel syndrome and functional dyspepsia.  
  TZP-301 (lead optimization) ghrelin antagonist for obesity.  

Technology
Tranzyme Pharma’s Macrocylic Template Chemistry (MATCH™) is a particularly rich source for novel drug candidates as it maintains the favorable characteristics exhibited by large biomolecules, such as tight receptor binding for high potency and selectivity, while eliminating the drawbacks associated with peptide and protein drugs, including poor metabolic stability, low oral bioavailability, lack of membrane permeability, high manufacturing costs, and antigenicity.

The major advantages of MATCH include:

  Exploits an unique compound class, macrocyclic small molecules (MW ~500), with exceptional flexibility for interacting with multiple target types  
  Proven effective on major druggable target classes (GPCRs, protein kinases, etc.)  
  Produces orally bioavailable compounds  
  Ability to find both agonists and antagonists  
  Produces information-rich primary hits  
  Designed for accelerated, resource-efficient lead optimization  

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www.tranzyme.com