| Name | Title | Contact Details |
|---|---|---|
Anand Shroff |
Chief Technology Officer | Profile |
ACADIA is a biopharmaceutical company focused on the development and commercialization of innovative medicines that address unmet medical needs in neurological and related central nervous system disorders. ACADIA has a pipeline of product candidates led by pimavanserin, which is in Phase III development as a potential first-in-class treatment for Parkinson’s disease psychosis. Pimavanserin is also in Phase II development for Alzheimer’s disease psychosis and has successfully completed a Phase II trial as a co-therapy for schizophrenia. ACADIA also has clinical-stage programs for chronic pain and glaucoma in collaboration with Allergan, Inc. and two advanced preclinical programs directed at Parkinson’s disease and other neurological disorders. All product candidates are small molecules that emanate from internal discoveries. ACADIA maintains a website at www.acadia-pharm.com to which ACADIA regularly posts copies of its press releases as well as additional information and through which interested parties can subscribe to receive e-mail alerts.
Bird Products Corporation is a Palm Springs, CA-based company in the Healthcare, Pharmaceuticals, and Biotech sector.
WeedMD is pre-approved under MMPR licensing for production and distribution of quality Medical Marihuana. We are retrofitting our 30,000 sq. ft facility in Ontario. Our group consists of qualified professionals committed to providing the best quality medicines to patients across Canada. WeedMD will be ready for distribution in April 2014.
ARCA biopharma, Inc. is a Colorado-based biopharmaceutical company developing genetically-targeted therapies for cardiovascular diseases. ARCA was founded on the belief that a personalized medicine approach to drug development, tailoring medical treatment to the individual genetic characteristics of each patient, can enable more effective therapies, improve patient outcomes and reduce healthcare costs. ARCA’s lead development program is intended to be a direct implementation of those ideas. The Company`s lead product candidate, GencaroTM (bucindolol hydrochloride), is an investigational, pharmacologically unique beta-blocker and mild vasodilator being developed for the prevention of atrial fibrillation in patients with heart failure. ARCA has identified common genetic variations in the cardiovascular system that it believes interact with Gencaro’s pharmacology and may predict individual patient response to Gencaro, giving it the potential to be the first genetically-targeted atrial fibrillation prevention treatment. We believe AF is an attractive indication for Gencaro because data from BEST, the previously conducted Phase 3 heart failure trial involving Gencaro in 2,708 HF patients, suggest Gencaro may have a potentially significant effect in reducing and/or preventing AF. Based on the BEST trial, we believe Gencaro`s prevention of AF in HF patients is pharmacogenetically regulated, similar to the effects on HF clinical endpoints. GENETIC-AF is a Phase 2B/3, multi-center, randomized, double-blind clinical trial comparing Gencaro to Toprolol-XL for prevention of symptomatic AF or atrial flutter (AFL) in patients with heart failure and/or reduced left ventricular ejection fraction (HFREF). ARCA plans to enroll only patients with the genetic variant of the beta-1 cardiac receptor which the Company believes responds most favorably to Gencaro. GENETIC-AF has an adaptive design, under which the Company plans to initiate it as a Phase 2B study in approximately 200 patients and then, depending on the results of an interim analysis by the trial Data Safety Monitoring Board (DSMB) and availability of additional financing, potentially transition the trial to a Phase 3 trial and enroll an estimated additional 420 patients. Under the collaboration with Medtronic, ARCA plans to conduct a substudy that will include continuous monitoring of the cardiac rhythms of patients enrolled during the Phase 2B portion of GENETIC-AF. These substudy patients will have heart rhythm monitoring via a Medtronic device, either a previously implanted cardiac resynchronization or defibrillation device, or a previously or newly inserted Reveal® LINQ Insertable Cardiac Monitor (ICM) System. The collaboration substudy will measure AF burden, defined as a patient’s actual time in AF regardless of symptoms. For the DSMB interim analysis, AF event rates, AF burden and components of the primary endpoint of the study, time to recurrence of symptomatic AF/AFL or death after electrical cardioversion to sinus rhythm, will be reviewed by the DSMB to determine if there is sufficient potential for a statistically significant efficacy signal in the overall Phase 2B/3 study population.
Copley Health System is one of the leading companies in Healthcare, Pharmaceuticals, and Biotech industry. Copley Health System is based in Morrisville, VT. You can find more information on Copley Health System at www.chsi.org