Showing posts with label Hot Topics. Show all posts
Showing posts with label Hot Topics. Show all posts

Thursday, January 29, 2015

January 2015 Round-Up of MS News and Research


  • 3-Year results from HALT-MS trial shows clinical efficacy in RRMS
  • Almost half of MS patients experience tremors, according to patient reports
  • MS panel recommends expanding No Evidence of Disease Activity (NEDA) to include neuropsychological measures
  • Cinnamon holds potential as an economical and effective treatment for MS
  • Fecal microbiota transplantation (FMT) may improve MS symptoms
  • Other Studies of Interest

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Monday, December 29, 2014

December 2014 Round-Up of MS News and Research


  • 3-Year results from HALT-MS trial shows clinical efficacy in RRMS
  • Almost half of MS patients experience tremors, according to patient reports
  • MS panel recommends expanding No Evidence of Disease Activity (NEDA) to include neuropsychological measures
  • Cinnamon holds potential as an economical and effective treatment for MS
  • Fecal microbiota transplantation (FMT) may improve MS symptoms
  • Other Studies of Interest

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Wednesday, November 26, 2014

November 2014 Round-Up of MS News and Research


  • Details of PML Death to be Added to Tecfidera Prescription Label
  • FDA Reverses Previous Rejection and Approves MS Drug Lemtrada
  • New Italian Study: Azathioprine is Not Inferior to Beta Interferon in Treating RRMS
  • Other Studies of Interest

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Hot Topics and MS Research News for November 2014

Tuesday, October 28, 2014

October 2014 Round-Up of MS News and Research

  • Psychiatric disorders may precede MS diagnosis
  • Non-drug therapies are more effective in combating MS-related fatigue
  • Reasons why people with MS fall more frequently
  • Other studies of interest   
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Hot Topics and MS Research News for October 2014

Friday, September 26, 2014

September 2014 Round-Up of MS News and Research

  • Melatonin supplementation may improve quality of life in MS patients
  • Actemra safely used in patient diagnosed with MS and RA
  • Long-term disability may be predicted by evoked potentials in 20 year MS study
  • Other studies of interest  
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Hot Topics and MS Research News for September 2014

Monday, July 28, 2014

July 2014 Round-Up of MS News and Research

  • TMJ is More Prevalent in MS Patients with Mild or Moderate Disability
  • Plegridy™ Approved for Adults with RRMS in Europe
  • Urinary Disorders and MS: Diagnosis, Treatment, and Quality of Life
  • Other studies of interest:  
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Hot Topics and MS Research News - July 2014

Friday, June 27, 2014

June 2014 Round-Up of MS News and Research

How common is sexual dysfunction in women with MS?
Sexual dysfunction is very common in MS but it is not highly discussed.  Studies report that up to 84.6% of women with MS experience at least one sexual dysfunction.  Approximately 34.8% of MS women experience 5 or more sexual dysfunctions while 12.9% experience 10 or more.  Symptoms include lower sex drive, decreased lubrication, poor clitoral erection, and lack of orgasm.  Other MS symptoms, such as bladder and bowel dysfunction, spasticity, pain, fatigue, depression, anxiety, and side effects of medication often contribute to sexual dysfunction.  More research is needed, but drugs such as sildenafil (a and alpha-blockers may improve lubrication.  Water-based lubricants and estrogen therapy may help with vaginal dryness, burning, and painful intercourse.  As antidepressants can interfere with orgasm, lower doses or a change of medication may be recommended.  Because of physical limitations of MS, women with MS may be advised to plan ahead for sex to manage timing, positioning, and fatigue, as well as prevent unwanted urinary or fecal incontinence.  Sex aids and extra-genital stimulation can provide erotic sensations.  Counseling can also help couples improve communication skills and increase sexual satisfaction (Cordeau, 2014).

Anti-seizure drug may be effective against pseudobulbar affect (PBA)
Pseudobulbar affect (PBA), also known as emotional incontinence, is a neurological disorder characterized by involuntary or uncontrollable episodes of laughing and/or crying.  It can occur in patients with an underlying neurological disease such as MS, Alzheimer’s, Parkinson’s, stroke, or traumatic brain injury.  Patients with PBA have an impaired ability to control their emotional reactions.  Very few studies have been published on PBA in people with MS and reported prevalence estimates range from 6.5 to 95%.  Dextromethorphan plus quinidine (Nuedexta) is the only FDA approved treatment for PBA.  A recent case report describes a 60 year old woman with MS who experienced incessant crying.  A brain MRI showed a new lesion next to her corpus callosum.  Her symptoms resolved within 3 days after doctors prescribed valproic acid (Depakote), but did not respond to Nuedexta (Johnson, 2014).

Do you want to know more about how the oral drugs for MS work?  
You can find out in the article, “Molecular pharmacodynamics of new oral drugs used in the treatment of multiple sclerosis,” published in the journal, Drug Design, Development and Therapy.  This article discusses the mechanism of action of each of the oral MS drugs, approved and still in development: fingolimod (Gilenya, Novartis), dimethyl fumarate (Tecfidera, Biogen Idec), teriflunomide (Aubagio, Genzyme), and laquinimod (Nerventra, Teva, not yet approved for use).  It also discusses the effects of each drug on the immune system, permeability of the blood-brain-barrier, and CNS cells (di Nuzzo, 2014).

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Hot Topics and MS Research News for June 2014

Tuesday, May 27, 2014

May 2014 Round-Up of MS News and Research

On May 23, 2014, Biogen Idec received good news as EMA-CHMP released a positive opinion for the marketing authorization of Plegridy, a pegylated interferon administered by subcutaneous injection once every two weeks at a dose of 125 mcg for adults with RRMS. Plegridy offers a less frequent dosing schedule among the interferon class of treatments for MS. The most common side effects include injection site erythema, influenza-like illness, pyrexia (fever), headache, myalgia (muscle pain), chills, injection site pain, asthenia (weakness), injection site pruritus (itching), and arthralgia (joint pain). Plegridy is being developed by Biogen Idec who also markets Tecfidera, Avonex, Tysabri, Fampyra, and Rituxan.

In the phase III ADVANCE study involving more than 1500 people with RRMS, Plegridy demonstrated a reduction in relapses, disability progression and the number of MS lesions when compared to placebo. Data from the first year of the study demonstrated that Plegridy significantly reduced annualized relapse rate (ARR) at one year by 36%, reduced the risk of 12-week confirmed disability progression by 38%, and significantly reduced the number of new or newly enlarging T2-hyperintense lesions when compared to placebo. The ADVANCE two-year data was consistent with the positive efficacy and safety results observed in year one.

In other research news:
A new study shows that diets that are lower in magnesium and folate are correlated with higher fatigue scores in multiple sclerosis patients.

Researchers studying stem cell rejection following transplantation discovered that mice infected with the neurotropic JHM strain of mouse hepatitis virus (JMHV) who were injected with human neural precursor cells (hNPCs) derived from human embryonic stem cells (hESCs) experienced improved motor skills and a reduction in neuroinflammation and demyelination about two weeks after the injections. Mice who had been paralyzed regained the ability to walk.  Further studies are warranted.

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Hot Topics and MS Research News for May 2014

Thursday, February 27, 2014

February Round-Up: MS News and Hot Topics

Relapse risk after switching from natalizumab (Tysabri) to fingolimod (Gilenya):

In another study, researchers collected data from patients with MS (n=333) who were switching from natalizumab (Tysabri) to fingolimod (Gilenya) after a mean of 31 natalizumab infusions (female to male ratio, 2.36; mean age, 41 years; 71% were JCV positive).  Data was collected regarding treatment with Tysabri, the duration and management of the washout period (WP) after stopping Tysabri, and any relapses or adverse events occurring during the WP and during the 6 months after patients started Gilenya. 

During the washout period, 27% of patients relapsed.  The risk for relapse was 3.2 times higher for patients who stopped natalizumab because of poor tolerance or lack of efficacy.  Washout periods shorter than 3 months were associated with 77% lower risk of relapse during the WP, but also with less disease activity before natalizumab treatment.  Twenty percent (20%) of patients relapsed during the first 6 months of treatment with fingolimod, while 3% stopped fingolimod due to issues with efficacy, tolerance, or compliance.  Researchers found that the occurrence of relapse during the WP was the only significant prognostic factor for relapse during fingolimod therapy (odds ratio, 3.80; P = .05). They also recommend that washout periods should be shorter than 3 months (Cohen, 2014).


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Hot Topics and MS Research News: February 2014

Friday, January 31, 2014

January Round-Up: MS News and Hot Topics

This week TEVA Pharmaceutical Inc announced that the FDA has approved the new 40mg/mL formulation of Copaxone (glatiramer acetate) designed to be injected subcutaneously three-times-a week.  Although TEVA hopes to transition current daily Copaxone users to the new formula, the original 20mg/mL formula will continue to be available, even after it goes off patent in May 2014 and faces generic competition from Mylan Inc.  The safety and efficacy of the longer-lasting dosing was demonstrated in the GALA study, results published in Annals of Neurology (Ann Neurol. 2013 Jun;73(6):705-13. doi: 10.1002/ana.23938. Epub 2013 Jun 28.)  Copaxone is prescribed for the treatment of relapsing-remitting MS to reduce the number of clinical exacerbations; and for patients who have experienced a first clinical episode and have MRI features consistent with MS. 

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Hot Topics and MS Research News: January 2014