Supernus Pharmaceuticals Inc. United States

Late stage specialty CNS pharmaceutical company with neurology and psych assets looking for partnerships for in and out license.

Website:
www.supernus.com
Business Type
Dr Woody Bryan
Vice President of Business Development and Licensing 

Teikoku Pharma USA United States

Teikoku Pharma USA Inc., a wholly-owned subsidiary of Teikoku Seiyaku Inc. of Japan, is an international specialty pharmaceutical company that develops, and manufactures pharmaceutical products. Teikoku focuses its efforts in three therapeutic areas; Pain Management, CNS and Oncology.  Teikoku's main product is Lidoderm® (Lidocaine 5% Patch) for PHN, distributed by Endo Pharmaceuticals in the US, Grunenthal GmbH in Europe. Our core technology platforms include; passive and active transdermal delivery systems as well as injectables. We are currently actively seeking to in-license/acquire later stage product for the US, Europe and Japan.

Business Type
Mr Francisco Bejar
LinkedIn logo Director, Business Development 

TherapeuticsMD United States

TherapeuticsMD (TXMD) is a publicly traded Women’s Health company located in South Florida.

TXMD currently has a national sales force calling on OB-GYNs in the US and a strong pipeline of late stage HRT products. We are currently pursuing in-licensing opportunities within the Women’s Health space and considering out-licensing International partners for our 3 late stage HRT products.

Business Type
Mr Robert Finizio
Chief Exectutive Officer 

Theravance Inc. 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
Mr Roland Gendron
LinkedIn logo Senior Business Development Associate 

Upsher-Smith Laboratories, Inc. United States

Upsher-Smith Laboratories, Inc. is pursuing improved drug therapies to improve people’s lives.  The evolution of their company is driven by the ever-changing needs of patients, physicians, pharmacists, and healthcare organizations.  Their perspective is not “more products,” but the right products that make people’s lives better.  At every level of their business, they are driven to be the best.

 

Upsher-Smith is actively pursuing product development opportunities in the therapeutic areas of epilepsy and Parkinson’s disease; their current product portfolio is focused in the areas of women’s health, dermatology, and cardiology.   

With a track record of successful collaboration in licensing and acquiring innovative products, Upsher-Smith is a trusted partner to many leading pharmaceutical companies, offering expertise in:   

 

  • Conducting clinical trials to support safety and efficacy
  • Preparing and managing submissions for the FDA review process
  • Commercialization and distribution of products to the retail and wholesale trade
  • Marketing and sales promotions through sales force, national conventions, professional advertising, and other media 

As an independent and privately held company, Upsher-Smith acts swiftly to create the right partnerships and connections that build upon their success.

 

On August 14, 2012, the company completed its acquisition of UK-based Proximagen Group plc, a European biotechnology company focused on the development and commercialization of novel therapeutics for diseases of the central nervous system and inflammation. 

 

Upsher-Smith also has offices in Plymouth, MN, Denver, CO and Morristown, NJ.

 

“Advancing pharmacotherapy.  Improving lifeSM”….  As the company evolves, Upsher-Smith’s goal remains the same:  to assist individuals in making the best use of medicines.  This not only means producing quality pharmaceutical products, but providing access to them as well.  The company promises to provide reliable, affordable products that have a daily impact to improve lives.

 

Upsher-Smith’s vision is to become a leader in providing therapies that empower people suffering from central nervous system (CNS) diseases to lead healthy, productive lives.

Business Type
Ms Lori Freese
Director, Strategic Portfolio Management 
Mr Mike McBride
Sr. Director, Industry Relations 

Vidara Therapeutics United States

We are a specialty pharmaceutical company intent on utilizing our proven business model of creating value through accretive product acquisitions or license agreements, sound marketing and distribution, and life cycle management.

In June 2012 we acquired Actimmune (Interferon Gamma) our first product acquisition.  Actimmune is indicated for reducing the frequency and severity of serious infections associated with Chronic Granulomatous Disease and delaying time to disease progression in patients with Severe, Malignant Osteopetrosis.  

We are seeking to acquire both commercial and late stage specialty niche therapeutics.  

 

Vidara is a fully financed and profitable specialty pharmaceutical company.  



Website:
www.vidararx.com
Business Type
Mr Rick McElheny
VP Business Development and Sales Operations 

Zosano Pharma United States

Zosano Pharma (ZP), a spin-off of J&J, offers a fully-developed and validated transdermal drug-delivery platform to deliver small molecules, peptides, proteins and vaccines on a band-aid like patch with the efficacy of injectables.

Totally pain-free, the ZP patch offers quick onset of action, delivers with the efficacy of an injection and is stable at room temperature. It has been successfully tested with 30 compounds. The most advanced product is PTH for severe osteoporosis with completed Ph2 studies. Rights to PTH for select Asian countries have been granted to Asahi-Kasei Pharma, Japan.

ZP products are produced in its own GMP manufacturing facility at a low cost and offer attractive margins versus currently-marketed injectables.

ZP products are attractive to patients (pain-free & don't require refrigeration), payors (priced competitively versus marketed products) and pharma companies (for life cycle extension with ZP IP extending to 2027).

Business Type
Mr Brian Rippie
LinkedIn logo Director, Business Development