ABOUT this BLOG and How to use it

WELCOME to Stu's Views & MS News. A product of MS Views and News, a Not-for-Profit [501c3] organization. Founded in 2008, we provide educational Multiple Sclerosis information via live seminars and via the internet.

Key-Notes: Our live seminars average approx 60 people per educational program. Our blog is visited over 2900 times per week and our website is visited by thousands each month.

Register at our website to receive our globally transmitted Multiple Sclerosis e-newsletter, currently being received in (90) Countries.

On this blog see our Directory, Archives, recent Blog Posts & so much more. Use the Blog Search box (enter a keyword). See our Facebook information AND Links to other MS Organizations & bloggers. Scroll through entire page, to find information that could EMPOWER You. At the Bottom of this page, see informational videos and some for fun.

Disclaimer: "Stu's Views & MS News" / 'MS Views and News' does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Like this blog? - CLICK "LIKE"

Monday, January 19, 2009

Interferon Delivered via a Nasal Spray

ms.about.com

Thursday January 15, 2009

There is potential good news coming for users of Avonex, Betaseron and Rebif. Those interferon treatments need to be injected and, let's just go ahead and say it, nobody likes injections.

Nerveda and Aegis Therapeutics announced that they have had successful preclinical results on a nasal spray to deliver the interferons.

The reason you simply can't have an pill for interferon treatment in multiple sclerosis is that this line of treatment relies on delicate protein molecules. Basically, protein molecules like to cling and bond to each other. If they do that too much, the immune system doens't react to them and produce the antibodies needed to reduce relaspe rates. A pill would be too unstable and too "bonded together" for it to be an effective interferon treatment.

A nasal spray would be a big deal. It's an effective (and much less painful) way to deliver interferon treatment. Expect to see clinical trails starting soon..

Leaving Comments, Suggestions and/or Questions, are Always Appreciated. - Thank you
============================================

2 comments:

Denver Refashionista said...

What will they think of next? This sounds promising...

Cherie said...

Lest anyone get too excited too early about this, "preclinical" means that there is an average of 4-7 years before it can come to market. This is not something you or I can do to alleviate site reactions at this point in time or in the foreseeable future.

I love the concept and hope it can be made real but we will not see it available outside of clinical trials for a long time.

If you want to participate in a trial, go to www.clinicaltrials.gov type in Multiple sclerosis then you can see which trials are enrolling for which drugs. It will also tell you the criteria for enrollment when you click onto individual trials.