ElMarino! That was me! When I was briefly hiding from someone who was sending me odd PMs. I got tired of the silly name and went back to plain old 'L'.. They were an NHS employee no less, who I new in real life, pretending to be a patient. Seriously!dignan wrote:I added BIIB033 (Anti-Lingo) to the phase 1 list based on a post from ElMarino. The post cites a Dow Jones article. The trial is also now listed in clinicaltrials.gov
http://english.capital.gr/news.asp?id=896271
http://www.clinicaltrials.gov/ct2/show/NCT01052506
Summary of the pipeline
Drug Pipeline

ssrn00, there is a "Natural Approach" forum that might be appropriate for your experience. If you're not sure about the rules of the board, they can be found here: http://www.thisisms.com/ftopict-39.html
Based on a posting from squiffy2 I added MIS416 to the phase 2 list. I like it because it's for progressive MS and Innate Therapeutics got some funding from Fast Forward:
<shortened url>
<shortened url>
Re: MIS416
The link to the Innate Therapeutics pdf didn't work. I found this article instead.
http://www.scoop.co.nz/stories/GE1009/S ... atment.htm
NHE
http://www.scoop.co.nz/stories/GE1009/S ... atment.htm
NHE
Thanks NHE, don't know what happened to that link. Daisy, yep, it's a drag. Actually, anything that's still in phase 2, even if it has been in phase 2 trials for a couple of years, is AT LEAST 4 years from approval, and 5 or 6 years is more realistic, and 8 years isn't unreasonable. Clinical trials take a long time, what with setting them up, recruiting, collection and analysis of results, regulatory filings etc.
Based on this post from gkalman, I added gilenya to the approved list:
http://www.thisisms.com/ftopict-13876.html
I think we are going to see new MS drug approvals every year from now on (until a cure).
http://www.thisisms.com/ftopict-13876.html
I think we are going to see new MS drug approvals every year from now on (until a cure).
- CureOrBust
- Family Elder
- Posts: 3374
- Joined: Wed Jul 27, 2005 2:00 pm
- Location: Sydney, Australia
http://molpharm.aspetjournals.org/conte ... 5.abstractElimination of a Hydroxyl Group in FTY720 Dramatically Improves the Phosphorylation Rate
...Our results suggest that AAL(R) is a better tool than FTY720 for in vivo studies with S1P analogs and would probably be a more effective immunosuppressant than FTY720...
Maybe this will one day reach the pipeline, if that cure dignan talks about doesn't come first.
I moved Amiloride from phase 1 to phase 2 (and it's a primary progressive trial!) based on this:
http://nres.npsa.nhs.uk/researchsummari ... 75297&p=38The primary objective of the study is to evaluate the effects of the drug, oral amiloride in primary progressive Multiple Sclerosis (MS) patients during 12 months of treatment. This project aims to evaluate the effect of oral amiloride using Magnetic resonance imaging (brain scans).
Participants will be drawn from those who previously completed the one year MRI study on primary progressive MS patients on specific treatment. Participants from that study will continue on to this present study. Participants will be given oral amiloride at a dose of 10mg a day daily for a period of 52 weeks.
All participants will be followed up for one year, undergoing 4 MRI scans. The participants will attend clinic visits at the same time for clinical outcomes and have 20ml of blood collected and urine sample at each visit.
- indigoinmotion
- Family Member
- Posts: 56
- Joined: Wed May 20, 2009 2:00 pm
I added a PPMS trial of Ocrelizumab to the phase 3 list, based on this clinicaltrials.gov listing.
On the one hand, this is GREAT news! Any time a new substance enters phase 3 it's a major step in the right direction. Just as importantly, it is being tested for PPMS, where the need is greatest.
On the other hand, this drug has a bit of a black cloud over it as there was a treatment-related death in the most recent phase 2 MS trial and it was discontinued as an experimental treatment for RA earlier this year due to side-effect concerns.
It's never straight forward when it comes to treating this disease, is it?
On the one hand, this is GREAT news! Any time a new substance enters phase 3 it's a major step in the right direction. Just as importantly, it is being tested for PPMS, where the need is greatest.
On the other hand, this drug has a bit of a black cloud over it as there was a treatment-related death in the most recent phase 2 MS trial and it was discontinued as an experimental treatment for RA earlier this year due to side-effect concerns.
It's never straight forward when it comes to treating this disease, is it?