Siponimod

Siponimod
Clinical data
ATC code None
Identifiers
Synonyms BAF-312
CAS Number 1230487-00-9
PubChem (CID) 44599207
ChemSpider 29315058
Chemical and physical data
Formula C29H35F3N2O3
Molar mass 516.26 g/mol
3D model (Jmol) Interactive image

Siponimod (or BAF312) is a selective sphingosine-1-phosphate receptor modulator for oral use that is an investigational drug for multiple sclerosis (MS). It is intended for once-daily oral administration.[1]

As of January 2016 it is in a phase III clinical trial for secondary progressive MS due to complete Dec 2016.

Clinical trials

(June 8, 2009) It is in Phase II trial. "A back-up compound for Fingolimod, BAF 312" is in Phase II studies.[2] It is being tested for the first time on people having multiple sclerosis. Worldwide 275 patients will participate in this phase II trial the outcome of which is to establish what the optimal dosage of BAF312 is for patients affected with Multiple Sclerosis for use in further trials. In order to identify "the optimal dosage", participants in group I will be randomly selected to take either placebo, or BAF312 in doses of 0.5 mg/day, 2 mg/day, or 10 mg./day and will be regularly controlled in order to measure and determine the effectiveness, the tolerability and the safety of the dosages.

A phase III trial should run from Dec 2012 to Dec 2016.[3]

Approvals and indications

None yet

Mechanism of action

Siponimod binds selectively to some of the Sphingosine-1-phosphate receptor forms - including Sphingosine-1-phosphate receptor 1 - found on lymphocytes and other cell types.

This binding inhibits the migration of the lymphocytes to the location of the inflammation (e.g. in MS).

BAF312, may be very similar to Fingolimod but preventing lymphopenia, one of its main side effects, by preventing egress of lymphocytes from lymph nodes. BAF312 may be more selective in the particular sphingosine-1-phosphate receptors (8 in number) that it modulates.[4] It is selective for the -1 and -5 SIP receptors.[1]

References


This article is issued from Wikipedia - version of the 4/17/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.