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NeuroDerm stock surges almost 20% as Parkinson's treatment shows promise

Posted: Published on December 31st, 2014

NEW YORK (MarketWatch) -- NeuroDerm Ltd. shares NDRM, +193.53% surged almost 20% in premarket trade Tuesday, after the company announced promising results from a trial of a treatment for Parkison's disease. The Israeli company said continuous, subcutaneous delivery of two liquid product candidates had a positive effect on plasma levels, suggesting the high dose version that is aimed at severe sufferers of the disease may be an effective alternative to current treatments that require surgery. The higher dose candidate, known as ND0612H, "is designed to be delivered continuously, thus we believe it should offer a simple and effective treatment option that will minimize the need for surgical intervention in advanced Parkinson's patients," Sheila Oren, vice president of clinical and regulatory affairs at the company, said in a statement. Shares of NeuroDerm, which went public in November, are down 15.2% on the month, while the S&P 500 has gained 1.1%. Excerpt from: NeuroDerm stock surges almost 20% as Parkinson's treatment shows promise … Continue reading

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NeuroDerm (NDRM) Stock Skyrockets to One-Year High After Encouraging Parkinson's Treatment Results

Posted: Published on December 31st, 2014

NEW YORK (TheStreet) -- Shares ofNeuroDerm (NDRM) skyrocketed more than 65% to a 52-week high of $10.31 in morning trading Tuesday after the Israeli company announced encouraging results from a trial for a treatment of Parkinson's disease. NeuroDerm announcedcontinuous, subcutaneous dosage of two of its proprietary liquid levodopa/carbidopa (LD/CD) product candidates, ND0612H and ND0612L, resulted in clinically significant plasma levadopa levels. The data indicates thatthe high dose version, ND0612H, meant for patients with severe Parkinson's disease, could be an effective therapy alternative to current treatments that require surgery. "Maintaining consistent levodopa concentrations has been the most significant hurdle in Parkinson's disease therapy," said Sheila Oren, MD, NeuroDerm's Vice President of Clinical and Regulatory Affairs. Exclusive Report: Jim Cramers Best Stocks for 2015 Jim Cramer and Stephanie Link reveal their investment tactics while giving advanced notice before every trade. Access the tool that DOMINATES the Russell 2000 and the S&P 500. Jim Cramer's protg, David Peltier, uncovers low dollar stocks with extraordinary upside potential that are flying under Wall Street's radar. View post: NeuroDerm (NDRM) Stock Skyrockets to One-Year High After Encouraging Parkinson's Treatment Results … Continue reading

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NeuroDerm Parkinson's Drug Shows Promise In Mid-Stage Study

Posted: Published on December 31st, 2014

Clinical-stage pharmaceutical company NeuroDerm Ltd. (NDRM: Quote), which went public in November, announced Tuesday topline results for a mid-stage study for its proprietary liquid levodopa/carbidopa (LD/CD) product candidates as a treatment for Parkinson's disease. Following the announcement, the company's shares are skyrocketing more than 49 percent in early deals. The company said the continuous, subcutaneous delivery of the liquid product candidates, ND0612H and ND0612L, led to clinically-significant plasma levodopa levels. The company added that ND0612H, the higher dose version, provided an effective alternative to current treatments that require surgery. "Maintaining consistent levodopa concentrations has been the most significant hurdle in Parkinson's disease therapy. The results from this study demonstrate that ND0612H can reach high LD plasma levels that, to date, could only be reached and maintained by products that require surgical intervention," said Sheila Oren, NeuroDerm's Vice President of Clinical and Regulatory Affairs. The phase IIa study was conducted on 16 patients with an advanced form of Parkinson's disease having motor fluctuations that was chronically treated with standard of care oral LD/CD. The primary endpoints of the study were to assess the safety, tolerability and pharmacokinetics (PK) of six dose regimens of ND0612H and ND0612L. The patients were treated with … Continue reading

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NeuroDerm soars on positive Parkinson's Phase II results

Posted: Published on December 31st, 2014

Rehovot-based Central Nervous Systems treatment drug developer NeuroDerm(Nasdaq:NDRM) has achieved positive results in a Phase IIa Pharmacokinetic Study of ND0612H and ND0612L for the treatment of Parkinsons disease. These results suggest that the high dose version, ND0612H, intended for severe Parkinsons disease patients, may provide an effective therapy alternative to current treatments requiring surgery. Following publication of the results the company's share price rose 194% to $18.14, giving a market cap of $308 million, well above Neuroderm's share price of $10 at its IPO last month, when it raised $50 million. NeuroDerm VP Clinical and Regulatory Affairs Dr. Sheila Oren said, Maintaining consistent levodopa concentrations has been the most significant hurdle in Parkinsons disease therapy. The results from this study demonstrate that ND0612H can reach high LD plasma levels that, to date, could only be reached and maintained by products that require surgical intervention. ND0612H is designed to be delivered continuously, thus we believe it should offer a simple and effective treatment option that will minimize the need for surgical intervention in advanced Parkinsons patients. NeuroDerm CEO Dr. Oded Lieberman said, These results add to the growing body of clinical data confirming our thesis that continuous, subcutaneous delivery of LD/CD … Continue reading

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ARIA Widens Sales Turf, NRX Skips A Beat, NDRM Triples On Parkinson's Study

Posted: Published on December 31st, 2014

Aquinox Pharmaceuticals Inc. (AQXP: Quote) has initiated dosing in a phase II clinical trial of AQX-1125 for the treatment of atopic dermatitis. The trial, dubbed KINSHIP, designed to enroll about 50 adult patients with mild to moderate atopic dermatitis is being conducted at clinical research centers in Canada. AQXP closed Tuesday's trading 6.46% higher at $7.25. ARIAD Pharmaceuticals Inc. (ARIA: Quote) has granted Angelini Pharma exclusive rights to commercialize leukemia drug Iclusig in seven Central and Eastern European countries. The seven countries include Bulgaria, the Czech Republic, Hungary, Poland, Romania, Slovakia and Slovenia. The commercial launches of Iclusig in these Central and Eastern European countries are expected to begin in 2015. With this distributorship in place, Iclusig will be available to patients with resistant and intolerant Philadelphia-positive leukemias in more than 23 countries in Europe. Net product revenues from sales of Iclusig were $14.5 million for the quarter ended September 30, 2014, an increase of 22% from the second quarter of 2014. ARIA closed Tuesday's trading at $6.82, down 1.23%. In after-hours, the stock was up 1.25% at $6.90. Idera Pharmaceuticals Inc.'s (IDRA: Quote) drug candidate IMO-8400 has been granted orphan drug designation by FDA for the treatment of Waldenstrm's … Continue reading

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Unique treatment at BC Childrens Hospital helps teen walk

Posted: Published on December 31st, 2014

An innovative treatment at BC Childrens Hospital has transformed 13-year-old Darrion Paynes life. Darrion suffers from cerebral palsy, and one of the many painful symptoms he developed, is whats known as a crouch gait. His knees were bent at 65 degrees and walking became extremely painful. Darrion Paynes knees were bent at 65 degrees Darrion still uses a wheelchair to get around, but thanks to this new therapy, hes no longer confined to the chair. Kind of surprised because I really wasnt able to move, says Darrion. BC childrens hospital is the only centre in North America using a unique surgical technique to correct crouch gait. Orthopedic surgeon Dr. Kishore Mulpuri says the method has fewer risks than other treatments. What we have done here is we have taken out roughly about 4-5cm segment of the bone and we fixed it with a stainless steel plate. Dr. Mulpuri has taken out roughly 4-5cm segment of the bone. Photo on right shows bone after it completely healed. The bent knee is down about 10-12 degrees. After surgery, the bent knee angle is reduced to between 10 and 12 degrees. The results have been dramatic for patients like Darrion. Of the six … Continue reading

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Report on remission in patients with MS three years after stem cell transplant

Posted: Published on December 31st, 2014

Three years after a small number of patients with multiple sclerosis (MS) were treated with high-dose immunosuppressive therapy (HDIT) and then transplanted with their own hematopoietic stem cells, most of the patients sustained remission of active relapsing-remitting MS (RRMS) and had improvements in neurological function, according to a study published online by JAMA Neurology. MS is a degenerative disease and most patients with RRMS who received disease-modifying therapies experience breakthrough disease. Autologous (using a patient's own cells) hematopoietic cell transplant (HCT) has been studied in MS with the goal of removing disease-causing immune cells and resetting the immune system, according to the study background. The Hematopoietic Cell Transplantation for Relapsing-Remitting Multiple Sclerosis (HALT-MS) study examines the effectiveness of early intervention with HDIT/HCT for patients with RRMS and breakthrough disease. The article by Richard A. Nash, M.D., of the Colorado Blood Cancer Institute at Presbyterian/St. Luke's Medical Center, Denver, and coauthors reports on the safety, efficacy and sustainability of MS disease stabilization though three years after the procedures. Patients were evaluated through five years. Study results indicate that of the 24 patients who received HDIT/HCT, the overall rate of event-free survival was 78.4 percent at three years, which was defined as … Continue reading

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Stopping Multiple Sclerosis with Stem Cell Transplants

Posted: Published on December 31st, 2014

Washington, DC - infoZine - Three-year outcomes from an ongoing clinical trial suggest that high-dose immunosuppressive therapy followed by transplantation of a person's own blood-forming stem cells may induce sustained remission in some people with relapsing-remitting multiple sclerosis (RRMS). RRMS is the most common form of MS, a progressive autoimmune disease in which the immune system attacks the brain and spinal cord. Three years after the treatment, called high-dose immunosuppressive therapy and autologous hematopoietic cell transplant or HDIT/HCT, nearly 80 percent of trial participants had survived without experiencing an increase in disability, a relapse of MS symptoms or new brain lesions. Investigators observed few serious early complications or unexpected side effects, although many participants experienced expected side effects of high-dose immunosuppression, including infections and gastrointestinal problems. Scientists estimate that MS affects more than 2.3 million people worldwide. Symptoms can vary widely and may include disturbances in speech, vision and movement. Most people with MS are diagnosed with RRMS, which is characterized by periods of relapse or flare up of symptoms followed by periods of recovery or remission. Over years, the disease can worsen and shift to a more progressive form. In the study, researchers tested the effectiveness of HDIT/HCT in … Continue reading

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Ebola Nurse May Be Offered Recovered Patients' Plasma

Posted: Published on December 31st, 2014

Nurse Pauline Cafferkey, who is battling Ebola at a London hospital, could be offered plasma from patients who have survived the virus. The treatment contains antibodies that should help fight the infection. British nurse William Pooley has donated plasma, Chief Medical Officer Dame Sally Davies confirmed. Other available treatments include antiviral drugs, but there are no stocks left of ZMapp - the drug used to treat Mr Pooley. He recovered from Ebola in September after being treated at the Royal Free Hospital, in Hampstead, north London, where Ms Cafferkey is currently being cared for. Having fought off the infection, his blood should help others do the same. Dame Sally said it would be up to Ms Cafferkey and her doctor to decide which treatments to use, adding: "The cornerstone of treatment remains fluid and electrolyte treatment." Ms Cafferkey was diagnosed with Ebola after returning to Glasgow from Sierra Leone, where she had travelled with a group of healthcare workers from Save the Children. She was said to be doing "as well as can be expected under the circumstances" by Scotland's First Minister Nicola Sturgeon. Another healthcare worker who was recently in West Africa and fell ill in the Scottish Highlands … Continue reading

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Heathrow cleared Ebola nurse Pauline Cafferkey for travel

Posted: Published on December 31st, 2014

An undated Cafferkey family handout photo of Scottish nurse Pauline Cafferkey, from Blantyre, who has been named as the healthcare worker being treated in Londons Royal Free Hospital for Ebola. Photograph: EPA Josh Halliday, Rowena Mason, Severin Carrell Health officials are facing serious questions over the UKs Ebola screening process after it emerged that a Scottish nurse who contracted the virus was cleared to leave Heathrow despite raising concerns about her health. Public Health England revealed that Pauline Cafferkey (39) told medics she was worried she had Ebola before being given the all-clear to catch a British Airways flight to Glasgow. Ms Cafferkey, a community nurse in Blantyre in south Lanarkshire, is the first Ebola patient to be diagnosed on British soil. She was receiving specialist treatment in an isolation unit at Londons Royal Free hospital on Tuesday . Sally Davies, the chief medical officer, admitted there were questions over whether officials should have been more precautionary about Ms Cafferkeys concerns, but stressed that the risk to the public was extremely low. Ms Cafferkey returned on Sunday night on a flight from Freetown to Heathrow via Casablanca. While at Heathrow, Ms Cafferkey was screened alongside other health workers but asked … Continue reading

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