Neothetics Tightens Guidance for Timing of Top-Line Pivotal Phase 3 Data
Neothetics, Inc., a clinical-stage specialty pharmaceutical company developing therapeutics for the aesthetic market, today tightened its guidance regarding the timing of release of top-line data for its two pivotal U.S. Phase 3 trials titled AbCONTOUR1 and AbCONTOUR2 of LIPO-202 to mid-December. LIPO-202 is the first non-invasive injectable drug candidate for reduction of central abdominal bulging due to subcutaneous fat in non-obese subjects.
Epic Sciences’ Chief Scientific Officer Named Leading Global Thinker by Foreign Policy Magazine
Epic Sciences' Chief Scientific Officer Dena Marrinucci, Ph.D., was named today by Foreign Policy magazine as one of this year’s 100 Leading Global Thinkers. Marrinucci will be honored at a gala in Washington, D.C. this evening.
Tragara Pharmaceuticals, Inc. (Tragara), a privately held clinical oncology company developing new treatments for cancer, announced today that China Oncology Focus Limited, an affiliate of Lee's Pharmaceutical Holdings Limited (Lee's Pharma), has licensed Tragara's oral multi-kinase inhibitor, TG02. Lee’s Pharma, a public biopharmaceutical company listed on the main board of the Hong Kong Stock Exchange (stock code: 950), has an operating history of over 20 years in China's pharmaceutical industry.
First US Commercial Appointment - Atlas Genetics appoints Keith Stauffer as VP Sales & Marketing
Atlas Genetics Ltd (“Atlas Genetics” or the “Company”), the ultra-rapid ‘test and treat’ molecular diagnostics company, today announces the appointment of Keith Stauffer as VP Sales and Marketing. Based in the newly opened Boston office, Keith will lead the launch and commercialisation of the Atlas Genetics io® System.
Epic Sciences, Inc. announced today a collaboration with the Abramson Cancer Center of the University of Pennsylvania (Penn) on multiple studies to explore biomarkers, identified by analysis of circulating tumor cells (CTCs) at a single cell resolution, that are predictive of response to personalized cancer therapeutics.
Clearside Biomedical, Inc., a clinical-stage biopharmaceutical company developing innovative first-in-class drug therapies to treat blinding diseases of the eye, today announced the U.S. Patent and Trademark Office (USPTO) granted U.S. Patent Application No. 14/523,243 as U.S. Patent No. 9,180,047 in a patent titled, "Apparatus and Methods for Ocular Injection."
Neothetics Reports Third Quarter 2015 Financial Results
Neothetics, Inc. (NASDAQ:NEOT), a clinical-stage specialty pharmaceutical company developing therapeutics for the aesthetic market, today reported financial results and business progress for the third quarter 2015.
Most men with advanced prostate cancer, whether initially treated through surgical or chemical castration, eventually develop drug-resistant tumors. Monitoring for drug resistant genetic mutations could inform selection of the next line of therapy. Complicating this is that prostate cancer frequently metastasizes extensively in the bone, which means monitoring may require repeated and sometimes painful bone biopsies, some of which may fail to recover a tumor sample.
Tobira Therapeutics Reports Third Quarter 2015 Financial Results
Tobira Therapeutics, Inc. ( NASDAQ : TBRA), a biopharmaceutical company developing novel treatments for non-alcoholic steatohepatitis (NASH) and other serious immuno-inflammatory and fibrotic diseases, today reported business highlights and financial results for the third quarter of 2015.
FDA Accepts PMA Submission for ReVision Optics’ Raindrop Near Vision Inlay
ReVision Optics, Inc. (RVO®), a leader in implantable presbyopia-correcting corneal inlay technology, announces that the U.S. Food and Drug Administration (FDA) has accepted and deemed fileable the company’s premarket approval (PMA) submission for the Raindrop® Near Vision Inlay. The Raindrop is a microscopic hydrogel inlay designed to correct presbyopia, thus reducing or eliminating the need for reading glasses. Acceptance and filing of the submission means the FDA has made a threshold determination that the Raindrop PMA submission is sufficiently complete to move forward in the FDA review and approval process.
The RMI group has completed sertain projects
The RMI Group has exited from the capital of portfolio companies:
Marinus Pharmaceuticals, Inc.,
Syndax Pharmaceuticals, Inc.,
Atea Pharmaceuticals, Inc.