We have applied our expertise in multivalency to discover product candidates and lead compounds in a number of therapeutic areas.

We believe that our lead product candidates have demonstrated in relevant preclinical models, potential advantages such as substantial increases in potency, duration of action and/or selectivity relative to existing medicines or potential medicines in late-stage clinical studies.

The table below summarizes the status of our most advanced product candidates for internal development or co-development. The table also includes the status of respiratory programs in which we have an economic interest that are being developed and commercialized by GSK pursuant to agreements with Theravance, Inc., now known as Innoviva, Inc.

THERAPEUTIC AREA STATUS
Program Phase 1 Phase 2 Phase 3 Filed Approved Collaborators
Infectious Disease
Multiple (ex-U.S.)¹
Telavancin: Bacteremia & cSSSI
Multiple (ex-U.S.)¹
Telavancin: Bacteremia & HABP/VABP
Multiple (ex-U.S.)¹
Telavancin: Primary Bacteremia
Multiple (ex-U.S.)¹
TD-1792: Gram+ MRSA
R-Pharm (ex-U.S.)
TD-6450: HCV
Trek Therapeutics
TD-1607: Gram+ MRSA
 
Respiratory
Revefenacin (TD-4208): COPD
Mylan
 
GASTROINTESTINAL
Axelopran (TD-1211): OIC
Axelopran (TD-1211)/Opiod FDC: Pain
Velusetrag: Gastroparesis
Alfa Wassermann (ex-U.S.)
TD-8954: ICU IV Prokinetic
Takeda
TD-1473, TD-3504: Ulcerative Colitis
 
Cardiovascular
TD-0714, TD-1439 : Heart Failure, Chronic Kidney Disease
TD-9855: nOH
 
Economic Interests
Closed Triple (FF/UMEC/VI): COPD
GSK & Innoviva, Inc.²
GSK & Innoviva, Inc.²
MABA, MABA/ICS (batefenterol, batefenterol/FF): COPD
GSK & Innoviva, Inc.²
Theravance Printable Pipeline

Notes:
¹ Data added to label for approved indications (cSSSI & HABP/VABP)
² We hold economic interest in future payments that may be made by GlaxoSmithKline plc (GSK) relating to certain programs, including “Closed Triple” (FF/UMEC/VI) (Fluticasone Furoate/Umeclidinium/Vilanterol), MABA/FF (batefenterol/FF), MABA monotherapy and other future products that may be combined with VI or MABA (batenfenterol)

Key:

  • CNS: Central Nervous System
  • COPD: Chronic Obstructive Pulmonary Disease
  • cSSSI: Complicated Skin and Skin Structure Infections
  • FF: Fluticasone Furoate
  • GI: Gastrointestinal
  • HABP/VABP: Hospital-Acquired and Ventilator-Associated Bacterial Pneumonia
  • HCV: Hepatitis C Virus
  • ICS: Inhaled Corticosteriod
  • MABA: Bifunctional Muscarinic Antagonist-Beta2 Agonist
  • MRSA: Methicillin-Resistant Staphylococcus Aureus
  • nOH: Neurogenic Orthostatic Hypotension
  • OIC: Opioid-Induced Constipation
  • UMEC: Umeclidinium
  • VI: Vilanterol

In the table above:

  • Status indicates the most advanced stage of clinical development that has been completed or is in process.
  • Phase 1 indicates initial clinical safety testing in healthy volunteers, or studies directed toward understanding the mechanisms of action of the drug.
  • Phase 2 indicates further clinical safety testing and preliminary efficacy testing in a limited patient population.
  • Phase 3 indicates evaluation of clinical efficacy and safety within an expanded patient population.
  • Filed indicates that a marketing application has been submitted to a regulatory authority.
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