Wed, 24/06/09 – 7:42 | No Comment

Amicus Therapeutics (Nasdaq: FOLD) announced it has commenced the U.S. registration Phase 3 trial with its investigational drug, Amigal(TM) (migalastat hydrochloride) for the treatment of Fabry disease. The Company has reached agreement with the …

Read the full story »
Aim to Cure

A focus on disease-specific efforts by pharmaceutical and biotech companies

Analysis

Read in depth analysis by industry experts on investing opportunities and business strategies

Company Profiles

Learn about corporate strategies, positioning and investing opportunities

Industry News

Stay on top of the industry with our industry news bulletin

Mutual Funds

Diversify to hedge your investment during economic turbulence

Home » Archive by Month

Article Archive for April 2009

New Studies On Once-Daily Extended Release Pramipexole Presented At American Academy Of Neurology Annual Meeting
Thursday, 30 Apr, 2009 – 1:00 | No Comment

New findings from two double-blind studies investigating the efficacy, safety and tolerability of pramipexole dihydrochloride tablets in an extended release, once-daily formulation, for the treatment of Parkinson’s disease (PD), are being presented at the American …

Pharmalink AB Completes Phase II Clinical Study With Renal Disease Drug Nefecon(R)
Thursday, 30 Apr, 2009 – 1:00 | No Comment

Pharmalink AB announced that it has completed its open Phase II trial evaluating the efficacy and safety of Nefecon(R) in IgA nephropathy, a glomerulonephritis leading to end-stage renal disease. Nefecon is an enteric formulation of …

Clinical Genomics Continues Progress In Developing Biomarker Portfolio For Colorectal Cancer Testing
Thursday, 30 Apr, 2009 – 1:00 | No Comment

Clinical Genomics Pty Ltd, an Australian biotechnology company, announced that Quest Diagnostics Incorporated, the world’s leading provider of diagnostic testing, information and services, has agreed to provide milestone payments over the next two years to …

Merz Pharmaceuticals Announces Results Of Three Clinical Trials With NT-201 (Botulinum Neurotoxin Type A Free From Complexing Proteins)
Wednesday, 29 Apr, 2009 – 1:00 | No Comment

Results from two prospective, double-blind placebo controlled multi-center studies in patients with cervical dystonia and blepharospasm, and pooled European efficacy and safety data in patients with focal dystonia and upper limb spasticity will be presented …

Dendreon Presents Preclinical Data Demonstrating Activity Of TRPM8 Agonist, D-3263, In Benign Prostatic Hyperplasia
Wednesday, 29 Apr, 2009 – 1:00 | No Comment

Researchers from Dendreon Corporation (Nasdaq: DNDN) presented preclinical data demonstrating the potential of D-3263, Dendreon’s orally bioavailable small molecule, which targets TRPM8 (a transmembrane cation channel protein), to treat benign prostatic hyperplasia (BPH). D-3263 …

Testosterone Undecanoate Achieves And Maintains Normal Testosterone Levels In Hypogonadal Men With Five Injections Per Year, New Data Show
Wednesday, 29 Apr, 2009 – 1:00 | No Comment

Endo Pharmaceuticals (Nasdaq: ENDP) released new long-term clinical trial data in men with hypogonadism who were treated for 21 months with testosterone undecanoate (NEBIDO(R) — 750 mg) injection, a long-acting testosterone replacement therapy in …

UTSA, Health Science Center Collaborate With Merck & Co. To Develop Chlamydia Vaccine
Tuesday, 28 Apr, 2009 – 5:00 | No Comment

The University of Texas at San Antonio (UTSA) and The University of Texas Health Science Center at San Antonio (Health Science Center) have announced an exclusive license and sponsored research agreement with Merck & Co., …

AMSA Members Join Connecticut Coalition Demanding Ban On Pharmaceutical Gifts
Tuesday, 28 Apr, 2009 – 5:00 | No Comment

Medical students from the University of Connecticut (UConn) and across the Northeast are joining the Connecticut Coalition for Prescription Reform on Tuesday, April 28th to lobby state representatives for mandated gift bans and disclosure of …

US, Canada, Japan And EU Sign International Agreement To Reduce Animal Use In Product Toxicity Testing Worldwide
Tuesday, 28 Apr, 2009 – 4:00 | No Comment

Representatives from four international agencies, including the director of the U.S. National Toxicology Program (NTP), have signed a memorandum of cooperation that could reduce the number of animals required for consumer product safety testing worldwide.
Read …

Phase 3 Trial Of Nexavar In Chemotherapy-Naive Patients With Advanced Melanoma Does Not Meet Primary Endpoint
Tuesday, 28 Apr, 2009 – 1:00 | No Comment

Bayer HealthCare Pharmaceuticals and Onyx Pharmaceuticals, Inc. (Nasdaq: ONXX) announced that a Phase 3 trial evaluating Nexavar(R) (sorafenib) tablets in patients with unresectable stage III or stage IV melanoma was stopped early following …

Cadence Pharmaceuticals Announces Presentations At Upcoming Scientific Conferences
Tuesday, 28 Apr, 2009 – 1:00 | No Comment

Cadence Pharmaceuticals, Inc. (Nasdaq: CADX) announced that data from clinical trials of its investigational product candidate, Acetavance(TM) (intravenous acetaminophen), will be presented at the American Society of Regional Anesthesia and Pain Medicine (ASRA) 34th …

Peregrine Pharmaceuticals Reports Positive Data In Second Phase II Bavituximab Breast Cancer Trial
Tuesday, 28 Apr, 2009 – 1:00 | No Comment

Peregrine Pharmaceuticals, Inc. (Nasdaq: PPHM), announced that updated preliminary data from its Phase II trial evaluating bavituximab in combination with carboplatin and paclitaxel in advanced breast cancer showed that nine of 14 evaluable patients …

First Annual Business And Medicine Symposium To Be Presented By Weill Cornell And Cornell’s Johnson School
Monday, 27 Apr, 2009 – 0:00 | No Comment

WHAT: A new yearly intercampus symposium exploring how business and medicine can collaborate to solve today’s health care challenges. Panel members will discuss and answer questions regarding the state of collaboration between industry, academia and …

Talley Environmental Care Granted U.S. EPA Approved Establishment Number
Sunday, 26 Apr, 2009 – 3:00 | No Comment

Talley Environmental Care™ is pleased to announce that it has been granted a U.S. Environment Protection Agency (EPA) approved establishment number 85343-GBR-001. Establishments that produce pesticides, active ingredients or devices, including …

Agreements Between Some Drugmakers, Insurers Link Prescription Drug Effectiveness To Price
Saturday, 25 Apr, 2009 – 11:04 | No Comment

Some drugmakers — encouraged by health insurers — have begun linking the prices of their medications to the drugs’ efficacy, the New York Times reports. According to some experts, the strategy could be a positive …

ANA598 Demonstrates Potent Antiviral Activity At All Dose Levels In Completed Phase Ib Study In Hepatitis C Patients
Saturday, 25 Apr, 2009 – 11:04 | No Comment

Anadys Pharmaceuticals, Inc. (Nasdaq: ANDS) announced that ANA598, the Company’s investigational non-nucleoside polymerase inhibitor, demonstrated potent antiviral activity at all dose levels and was well tolerated in a Phase Ib study in which patients …

IBM And Golden State Medical Supply Create Drug Safety Model To Help Combat Counterfeiting
Saturday, 25 Apr, 2009 – 1:00 | No Comment

IBM (NYSE: IBM) and contract manufacturer and third party logistics provider Golden State Medical Supply (GSMS) announced the two companies have worked together to help drug companies comply with stringent prescription drug pedigree regulations …

Pharmatech Oncology Launches New Data Management Business Unit
Saturday, 25 Apr, 2009 – 1:00 | No Comment

Pharmatech Oncology, Inc., a Research Management Organization (RMO) headquartered in Denver, Colorado, announces the launch of their Data Management business unit to the bioscience and pharmaceutical industries. The Pharmatech Oncology Data Management business unit is …

InterMune Reports Presentation Of Triple Combination Study Of ITMN-191 At European Association For The Study Of The Liver (EASL)
Saturday, 25 Apr, 2009 – 0:00 | No Comment

InterMune, Inc. (Nasdaq: ITMN) announced that results from a 14-day Phase 1b clinical study of ITMN-191 (R7227) in combination with the current standard of care were presented by Stefan Zeuzem, M.D., of the J.W. …

Intarcia Therapeutics, Inc. Announces Completion Of Enrollment Of ITCA 650 Phase 1b Study For The Treatment Of Type 2 Diabetes
Saturday, 25 Apr, 2009 – 0:00 | No Comment

Intarcia Therapeutics, Inc. announced the completion of patient accrual to a phase 1b clinical study evaluating ITCA 650 (DUROS(R) continuous delivery of exenatide). The study is being conducted at multiple centers in the United States …