Pipeline

Our research and discovery initiatives, driven by our proprietary chemical technology, have yielded novel compounds targeting significant bacterial threats. These compounds are now in the clinical trial phase of development.

 

XERAVA (eravacycline)


XERAVA.com

TP-271


  • A fully synthetic tetracycline antibiotic in phase 1 clinical testing
  • Development program targets respiratory disease caused by bacterial biothreats and antibiotic-resistant public health pathogens
  • Potent activity in vitro against Gram-negative and Gram-positive pathogens associated with respiratory tract infections
  • National Institutes of Health’s National Institute of Allergy and Infectious Diseases funding supports preclinical development and phase 1 study
  • Granted Qualified Infectious Disease Product and Fast Track designations by the U.S. Food and Drug Administration for both IV and oral formulations
  • Positive safety and pharmacokinetic data from IV single-ascending and multiple-ascending dose studies

TP-6076


  • A fully synthetic tetracycline antibiotic in phase 1 clinical development
  • Potent activity in vitro against multidrug-resistant Gram-negative pathogens
  • Phase 1 multiple-ascending dose study complete
  • Selected to receive $4 million in funding from Combating Antibiotic Resistant Bacteria Biopharmaceutical Accelerator (CARB-X) to support development

Investigational Products

Multiple investigational compounds are currently in the discovery phase. Our proprietary technology for tetracycline synthesis gives access to a broad range of molecules that would be inaccessible by semisynthetic methods and provides a powerful engine for the discovery and potential development of new tetracycline drugs.

If you are interested in access to a Tetraphase investigational therapy, please click here for additional information.

Expanded Access

Tetraphase is committed to developing novel therapeutics for serious illnesses. Prior to regulatory approval, the optimal way to gain access to one of our investigational products is to participate in one of our ongoing clinical trials. For information about ongoing clinical trials, please consult
www.clinicaltrials.gov.

However, there may be some patients who cannot participate in clinical trials and would like to
seek access to investigational products prior to approval. Although we do not have a formal
Expanded Access policy, we may consider requests for access to medicine outside of a clinical trial
on an individual basis when submitted through a physician.

Requests for Expanded Access can be submitted via the following channels:

Tetraphase will aim to respond to these requests within 24-48 hours.

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