Mr Roland Gendron United States

Theravance, Inc. - Medicines that Make A Difference®

www.theravance.com   

 

 

 

Theravance, Inc. 

901 Gateway Boulevard

94080 South San Francisco, California

United States

 

Founded 1998

223 employees (worldwide)

Public

 

 

Theravance is focused on the discovery & development of small molecule medicines for infectious disease, respiratory disease, gastrointestinal motility dysfunction, CNS disorders, pain management, and cardiovascular disease. We are seeking partners in all territories of the world for our US/EU/Canada approved VIBATIV® (telavancin) antibiotic for serious hospital infections and for our clinical-stage programs for opioid-induced constipation, chronic constipation, diabetic gastroparesis, COPD, asthma, adult ADHD, fibromyalgia, chronic pain, hospital-acquired MRSA pneumonia, Alzheimer’s Disease, and post-operative ileus. We also have preclinical programs targeting HCV, hypertension, heart failure, kidney disease/injury, and PAH.

Programs available for partnering include:

Approved NME

 

VIBATIV® (telavancin) i.v. lipoglycopeptide antibiotic – approved for complicated skin and skin structure infections (cSSSI) in the US and Canada; approved for MRSA nosocomial pneumonia (NP) in the EU.

Clinical Programs

 

TD-1211 for opioid-induced constipation – oral peripherally-selective mu-opioid receptor antagonist (PuMA) –  positive topline Phase 2b results announced July 2012, Phase 3 ready.

 
TD-4208 for COPD – inhaled long-acting muscarinic receptor antagonist (LAMA) – completed Phase 2a single-dose study, Phase 2b ready.

 

TD-9855 for chronic pain, adult ADHD, and other CNS disorders – oral monoamine reuptake inhibitor (MARIN) – in Phase 2 for adult ADHD; Phase 2 planned for fibromyalgia.

 

TD-1792 for serious Gram-positive infections including hospital-acquired MRSA pneumonia – i.v. glycopeptide-cephalosporin heterodimer antibiotic – completed Phase 2 vs. vancomycin. 

Pre-Clinical Programs

 

TD-8954 for post-operative ileus – i.v. highly-selective 5-HT4 receptor agonist – in Phase 1.

oral heterodimeric

 

NS5A inhibitor for HCV – in IND-enabling safety studies.

Dual function angiotensin receptor blocker / neprilysin inhibitor (ARNI) for hypertension, heart failure – Pre-clinical.

Neprilysin inhibitor for hypertension, heart failure, kidney disease/injury, PAH – Pre-clinical.

 

 

Primary ticker symbol

THRX

Primary stock exchange

NASDAQ

Summary Products / Services / Technologies

VIBATIV® (telavancin) for serious Gram-positive hospital infections
Relvar™ or Breo™ (FF/VI) for COPD, asthma
Umeclidinium bromide/vilanterol (UMEC/VI)  for COPD
MABA (Bifunctional Muscarinic Antagonist-Beta2 Agonist) for COPD
TD-1211 (PuMA) for opioid-induced constipation
Velusetrag / TD-5108 (5-HT4 agonist) for GI motility disorders
TD-4208 (LAMA) for COPD, asthma
TD-9855 (MARIN) for chronic pain, fibromyalgia, adult ADHD
TD-1792 (Gp-Ceph) for serious Gram-positive hospital infections
Velusetrag / TD-5108 (5-HT4 agonist) for Alzheimer's Disease

TD-8954 (5-HT4 agonist) for post-operative ileus
TD-2872 (NS5a inhibitor) for HCV

TD-0212 (ARNI) for hypertension, heart failure
NEPi for hypertension, heart failure, kidney disease/injury, PAH

 

Collaborations and Clients

Partnering strategy/collaborations

Theravance’s key programs include:  Relvar™ or Breo™ (FF/VI), umeclidinium bromide/vilanterol (UMEC/VI) and MABA (Bifunctional Muscarinic Antagonist-Beta2 Agonist), each partnered with GlaxoSmithKline plc

Business Type
Theravance Inc.
LinkedIn logo Senior Business Development Associate 

Tassos Gianakakos United States

MAP Pharmaceuticals is a biopharmaceutical company focused on developing and commercializing new therapies to address undermet patient needs in neurology. The Company is developing LEVADEX®, an orally inhaled investigational drug for the acute treatment of migraine. The U.S. Food and Drug Administration (FDA) reviewed the New Drug Application (NDA) for LEVADEX and on March 26, 2012, the Company received a Complete Response letter with respect to this NDA. MAP Pharmaceuticalshas entered into a collaboration agreement with Allergan, Inc. to co-promote LEVADEX to neurologists and pain specialists in the U.S. and Canada. The Company also applies its proprietary drug particle and inhalation technologies to generate new pipeline opportunities by enhancing the therapeutic benefits of proven drugs, while minimizing risk by capitalizing on their known safety, efficacy and commercialization history. Additional information about MAP Pharmaceuticals can be found athttp://www.mappharma.com.

Business Type
MAP Pharmaceuticals, Inc.
Senior Vice President and Business Development & Corporate Development 

Dr Paul Glidden United States

NanoSmart has developed and patented, a targeted drug delivery platform using human-derived, autoimmune antibodies capable of targeting many different kinds of tumors.  NanoSmart’s antitumor antibody, is not tumor-marker specific, but rather targets the areas of necrosis present in all solid tumors; including breast, lung, prostate, and rare cancers like Ewing’s Sarcoma.  Normal tissues do not have areas of necrosis and are not targeted.

 

NanoSmart is encapsulating off-patent FDA-approved drugs within liposomes coated with NanoSmart’s human-derived antibodies, thus creating an immunoliposome.  The liposome that encloses the active pharmaceutical ingredient protects healthy tissues while traveling to its target, and then slowly releases the drug over time.  NanoSmart’s antibody will then bind to the necrotic areas present in the middle of solid tumors and at the surrounding tumor site.

 

The end-result of using NanoSmart’s platform is a superior safety and efficacy profile for any drug that is adapted to our system.  Many different formulations can be developed by simply replacing one drug with another.  Each formulation is novel, patentable, and non-tumor specific (i.e. targets multiple cancers), and can be developed at a fraction of the cost and time typically associated with new drug development (i.e. IND to NDA in approximately 2-3 years).

 

Business Type
NanoSmart Pharmaceuticals, Inc.
Vice President Research & Development 

Jonathan Goldman United States

MannKind’s patient-focused oral inhalation drug delivery technologies include a dry powder formulation capability coupled with an innovative, elegant, breath-powered delivery device. We are applying these technologies to facilitate partnered drug development programs for proprietary compounds.

 

MannKind has numerous collaborations across therapeutic areas that demonstrate the efficacy and safety of the technologies. Patients self-administer these dry powder formulations with small, easy-to-use, breath-powered inhalers. Following inhalation, drugs are absorbed very rapidly, essentially mimicking intra-arterial administration. MannKind has evaluated this versatile pulmonary drug delivery platform across multiple therapeutic areas, including diabetes, metabolism, respiratory disease, osteoporosis and pain.

 

For companies interested in exploring the feasibility of a Technosphere formulation using their own active pharmaceutical ingredient (API), MannKind offers a feasibility evaluation. These evaluations involve preparation and characterization of API/Technosphere formulations. These powders are tested for performance in MannKind’s inhalers. Additionally, MannKind works with the partner to test these powders in relevant nonclinical PK/PD models. These studies can often been completed within 6 months. 

 

MannKind seeks to establish partnerships to build therapeutic programs of significant clinical and commercial value. Whether through strategic alliances, licensing arrangements and/or research collaborations, MannKind's partnering approach is based on a flexible, creative methodology designed to establish mutually beneficial relationships that are positioned to capture upside potential beyond what either partner could achieve individually.

Jonathan Goldman
MannKind Corporation
Senior Director of Business Development and New Product Development 

Angus Grant

Celgene
Vice President of Business Development and Global Alliances 

David Greenwald, Ph.D. United States

Relay brings you BD Live! – a software solution providing business intelligence to life science professionals to validate opportunities, discover new assets, and assess their pipelines against their competitors. BD Live! provides real-time trend monitoring and comparative asset analysis and complements existing evaluation models to help business development professionals hone in on promising new technologies and avoid transactions that have limited potential.

Website:
www.relaytm.com
Business Type
David Greenwald, Ph.D.
Relay Technology Management
LinkedIn logo Managing Director 

John Gustofson

AstraZeneca
Director of Business Development