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I HAVE PARKINSON'S DISEASES AND THOUGHT IT WOULD BE NICE TO HAVE A PLACE WHERE THE CONTENTS OF UPDATED NEWS IS FOUND IN ONE PLACE. THAT IS WHY I BEGAN THIS BLOG.
I COPY NEWS ARTICLES PERTAINING TO RESEARCH, NEWS AND INFORMATION FOR PARKINSON'S DISEASE, DEMENTIA, THE BRAIN, DEPRESSION AND PARKINSON'S WITH DYSTONIA. I ALSO POST ABOUT FUNDRAISING FOR PARKINSON'S DISEASE AND EVENTS. I TRY TO BE UP-TO-DATE AS POSSIBLE.
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Monday, February 9, 2015
Our Amazingly Plastic Brains

23andMe: Quest for Parkinson's cure opens door to genetic data mining
Singing therapy helps Parkinson's patients
Saturday, February 7, 2015
UCB announces positive top-line results from two phase 3 studies of Neupro to treat Parkinson’s disease
| Brussels, Belgium
Saturday, February 07, 2015, 10:00 Hrs [IST] |
UCB announced positive top-line results from two phase 3 studies evaluating Neupro (rotigotine transdermal patch) in the treatment of patients in China with early- and advanced-stage idiopathic Parkinson’s disease.
Results from the phase 3 study in patients with early-stage Parkinson’s disease demonstrated that rotigotine transdermal patch significantly improved symptoms when compared to placebo. In addition, data from the phase 3 study in advanced Parkinson’s disease showed that patients treated with rotigotine had a significantly greater decrease in their ‘off’ time, or periods of poor mobility, slowness and stiffness, compared to those patients taking placebo. The adverse event profile observed in these studies and in this Chinese population were consistent with that known for rotigotine. Based on the positive results UCB intends to submit a regulatory application in China in 2015 for Neupro in the treatment of early- and advanced-stage Parkinson’s disease. “Parkinson’s disease is a chronic and progressive neurological disease that can significantly impact patients’ lives. The positive results from the two Phase 3 studies in China evaluating Neupro in Parkinson’s disease is a significant milestone to making Neupro available to more patients and healthcare professionals worldwide. Subject to regulatory approval, we hope to deliver Neupro in China as a new treatment option to patients with early- and advanced-stage Parkinson’s disease,” says Professor Dr. Iris Loew-Friedrich, chief medical officer and executive vice president, UCB. One of the two phase 3 studies was a multicentre, randomised, double-blind, parallel-group, placebo-controlled, 24-week study that evaluated the efficacy and safety of rotigotine (escalating weekly dose starting with daily doses of 2 mg/24 hours to 8 mg/24 hours) in 247 adult patients (30 years and older) with early-stage idiopathic Parkinson’s disease. The primary efficacy variable was the change in the sum of the score from the Activities of Daily Living scale and motor examination in the Unified Parkinson's Disease Rating Scale (UPDRS) from baseline to the end of the maintenance period. The second phase 3 study was a multicenter, randomized, double-blind, parallel-group, placebo-controlled, 12-week study that evaluated the efficacy and safety of rotigotine (escalating weekly dose starting with daily doses of 4 mg/24 hours to 16 mg/24 hours) in 346 adult patients (30 years and older) with advanced-stage idiopathic Parkinson’s disease who were not well-controlled on levodopa. The primary efficacy variable was the change in absolute time spent "off" from baseline to the end of the double-blind maintenance period. Results from these studies will be presented at upcoming international congresses. Today, Neupro, a transdermal patch, is currently available as a treatment for Parkinson’s disease in over 46 countries worldwide, including the US, the European Union and Japan. Neupro is currently not approved in China for the treatment of Parkinson’s disease. Parkinson's disease is a progressive and chronic neurological disease characterised by the physical motor symptoms of resting tremor, muscle rigidity and slowness of movement. Symptoms not related to movement (non-motor symptoms) can also occur and include pain, sleep disturbances and depression. It is estimated that 6.3 million people are living with Parkinson’s disease worldwide. The age of onset is usually over 60 years. Although it is estimated that 1 in 10 people are diagnosed before the age of 50. Neupro (rotigotine) is approved in the European Union for the treatment of the signs and symptoms of early-stage idiopathic Parkinson’s disease, as monotherapy (i.e. without levodopa) or in combination with levodopa, i.e. over the course of the disease, through to late stages when the effect of levodopa wears off or becomes inconsistent and fluctuations of the therapeutic effect occur (end of dose or on-off fluctuations). Neupro® is also approved in the European Union for the symptomatic treatment of moderate to severe idiopathic Restless Legs Syndrome in adults. Neupro (rotigotine) is approved in the European Union for the treatment of the signs and symptoms of early-stage idiopathic Parkinson’s disease, as monotherapy (i.e. without levodopa) or in combination with levodopa, i.e. UCB, Brussels, Belgium (www.ucb.com) is a global biopharmaceutical company focused on the discovery and development of innovative medicines and solutions to transform the lives of people living with severe diseases of the immune system or of the central nervous system. With more than 8500 people in approximately 40 countries, the company generated revenue of € 3.4 billion in 2013. |
| http://health.einnews.com/article/248621659/g_XwdqLF8QXEtgzk |
Thursday, February 5, 2015
Biomarkers Show Potential for Parkinson's Diagnosis
Updated: Feb 4th 2015
Tips for Parkinson’s Disease Patients Switching from Sinemet or Madopar to Rytary (IPX066)
The What’s Hot in Parkinson’s disease blog written in April 2013 featured a new extended release dopamine drug called IPX066. This new dopamine formulation achieved full FDA approval in January 2015. The drug is now sold under the name Rytary. At National Parkinson Foundation we frequently hear from Parkinson’s disease patients that current carbidopa/levodopa medication preparations fail to adequately address disease-related symptoms. In this month’s What’s Hot column we will update you on important information on Rytary, and also offer a few tips for switching.
Medication dosages taking too long to “kick in” and start working
Too many medication dosage intervals (e.g. taking medications every 1-2 hours
The new formulation of carbidopa/levodopa extended release (IPX066/Rytary), is different than its predecessors. It contains special beads designed to dissolve at different rates within the stomach and the intestines. The medication capsule was designed to provide longer lasting benefit for patients with Parkinson’s disease. The randomized study included 393 Parkinson’s disease patients who reported at least of 2.5 hours of “off time,” defined as periods when they felt the medication was not working. The authors aimed to improve the number of hours of “off time” each day for patients randomized to the new extended release formulation (IPX066/Rytary) as compared to the older and standard regular release carbidopa/levodopa. The results revealed that the group on extended release formulations took less overall medication dosages (3.6 vs. 5 doses per day); however they also took more total pills. The daily “off-time” improved by over an hour each day in the extended release formulation. Both medications in this trial were safe and well tolerated.
If we return to the six areas (listed above in bullet points) where Parkinson’s disease patients have been seeking improved medication formulations, Rytary was observed to improve issues in two categories: wearing off between dosages, and improvement by increasing the time interval between dosages. The results of the current study cannot be widely applied to patients with severe dyskinesia, severe on-off fluctuations, and later stage disease. The new extended release formulation also increased the total blood-stream levodopa exposure by 30-40% as compared to conventional immediate release levodopa. Increasing levodopa in the bloodstream is thought to decrease the threshold for dyskinesia, and this has been observed with other Parkinson’s drugs such as Entacapone and Stalevo. Although dosed less frequently, the extended release formulation can require more total pills per day (see FDA conversion table below). The authors of the Rytary study felt that a newer formulation of the same drug, which they anticipate will be used in future clinical practice, would allow for a decrease in pill number.
Though it is unknown who the “best” patients in clinical practice will be, it is suspected that
benefit could possibly be obtained by adding a dose of Sinemet or Madopar rather than
There may be select patients who can take a Rytary dose that is approximately three times
Dosages of Rytary are not interchangeable with other levodopa (Sinemet or Madopar)
The capsules can be opened and the contents sprinkled onto foods such as apple sauce, if
The most important information for patients and families is to avoid magical thinking when
It will be important for the patient, family, and doctor to discuss the symptoms and optimize
The FDA label on Rytary provides a nice chart on general (approximate) recommendations
1: Pahwa R, Lyons KE, Hauser RA, Fahn S, Jankovic J, Pourcher E, Hsu A, O'Connell M, Kell S, Gupta S; APEX-PD Investigators. Randomized trial of IPX066, carbidopa/levodopa extended release, in early Parkinson's disease. Parkinsonism Relat Disord. 2014 Feb;20(2):142-8. doi: 10.1016/j.parkreldis.2013.08.017. Epub 2013 Sep 5. PubMed PMID: 24055014.
2: Hauser RA, Hsu A, Kell S, Espay AJ, Sethi K, Stacy M, Ondo W, O'Connell M, Gupta S; IPX066 ADVANCE-PD investigators. Extended-release carbidopa-levodopa (IPX066) compared with immediate-release carbidopa-levodopa in patients with Parkinson's disease and motor fluctuations: a phase 3 randomised, double-blind trial. Lancet Neurol. 2013 Apr;12(4):346-56. doi: 10.1016/S1474-4422(13)70025-5. Epub 2013 Feb 26. PubMed PMID: 23485610.
3: Hauser RA. IPX066: a novel carbidopa-levodopa extended-release formulation. Expert Rev Neurother. 2012 Feb;12(2):133-40. doi: 10.1586/ern.11.195. Review. PubMed PMID: 22288668.
4: http://www.accessdata.fda.gov/drugsatfda_docs/label/2015/203312s000lbl.pdf
5: Okun MS. Parkinson’s Treatment: 10 Secrets to a Happier Life. Createspace, 2013.


