Forecast Insight - Parkinson's Disease - Market upgrade following ... Live-PR.com (Pressemitteilung), Austria - Nov 25, 2008 Over the next 5 years Azilect is expected to become a standard first-line therapy, with sales peaking in 2013, making it the market leading Parkinson?s ...
H. Lundbeck (CPH:LUN) Lundbeck Increases Its Research And ... ABN Newswire (press release), Australia - Nov 11, 2008 Events since the latest interim report Azilect? In a clinical trial (ADAGIO), Azilect? proved able to slow progression of Parkinson's disease. ...
Brain Teasers Express Healthcare Management, India - Nov 13, 2008 Parkinson's disease-Treatment for Parkinson's has evolved considerably over the last three decades. Existing treatments day can improve symptoms, ...
Teva Pharma Set to Move Higher Investerms.com, CA - Nov 21, 2008 The Company has an innovative pharmaceutical business, whose principal products are Copaxone for multiple sclerosis and Azilect for Parkinson?s disease, ...TEVA
Another strong quarter sees profits soar at Teva Pharma Times (registration), UK - Nov 6, 2008 Sales of Azilect (rasagiline) for Parkinson?s disease reached $46 million, up 38%, while global respiratory revenues were flat at $177 million. ...TEVA
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Ahead of the Bell: Teva shares edge up Forbes, NY - Jul 8, 2008 He thinks the Parkinson's disease treatment Azilect is more important to Teva stock than Copaxone is, and he expects the company to report full details of a ...TEVA
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The FDA ( U.S. Food and Drug Administration ) has approved Azilect ( Rasagiline ) for the treatment of Parkinson's disease.
The drug is a monoamine oxidase type--B ( MAO-B ) inhibitor that blocks the breakdown of dopamine, a chemical that sends information to the parts of the brain that control movement and coordination.
Parkinson's disease is a chronic, progressive neurodegenerative condition caused by the destruction of the brain cells that produce dopamine. As the level of this chemical declines, messages from the brain telling the body how and when to move are delivered more slowly, leaving a person incapable of initiating and controlling movements in a normal way.
Azilect was approved for use as an initial single drug therapy in early Parkinson's disease, and as an addition to Levodopa in more advanced patients.
Levodopa is a standard treatment for Parkinson's disease.
The safety and effectiveness of Azilect was demonstrated in three 18- to 26-week controlled clinical trials.
One of the studies compared the effects of Azilect with the effects of placebo in 404 patients with early Parkinson's. Compared with patients on placebo, the condition of patients on Azilect showed significantly less worsening on a rating scale that measures the ability to perform mental and motor tasks as well as daily living activities.
The other two studies compared the effects of Azilect with placebo when taken together with Levodopa by over 1100 patients with more advanced Parkinson's.
In these studies, patients using Azilect together with Levodopa had significantly less time per day with relatively poor function and mobility as compared with patients on Levodopa and placebo.
Azilect may be associated with hypertensive crisis if patients also consume tyramine-rich foods, beverages ( such as cheese and red wine ) or dietary supplements or amines contained in many cough/cold medications. Therefore, patients will need to avoid these sources of tyramine and amines when taking Azilect.
As with most other medications for Parkinson's, Azilect has the potential to cause involuntary movements ( dyskinesias ), hallucinations and lowered blood pressure.
During development, melanoma was diagnosed in a small number of patients treated with Azilect. Although the FDA has concluded that the available data do not establish that Azilect is associated with an increased risk for melanoma, it appears that compared to the general population, patients with Parkinson's disease have an increased risk for this form of skin cancer.
In order to address the question of whether or not Azilect itself increases such risk, the drug's manufacturer will perform a Phase 4 ( postmarket ) study.
The product labeling will recommend that patients undergo periodic dermatologic examinations.