Tuesday, June 29, 2010

CYCC - Cyclacel Pharmaceuticals Drug 'Sapacitabine' was Granted Orphan Drug Status by the FDA for the Treatment of Myelodysplastic Syndrome:


Orphan Status is verified on the FDA website:

Here is some information about what Orphan Status means...

CONGRESSIONAL FINDINGS FOR THE ORPHAN DRUG ACT

The Congress finds that...

(1) there are many diseases and conditions, such as Huntington's disease, myoclonus, ALS (Lou Gehrig's disease), Tourette syndrome, and muscular dystrophy which affect such small numbers of individuals residing in the United States that the diseases and conditions are considered rare in the United States;

(2) adequate drugs for many of such diseases and conditions have not been developed;

(3) drugs for these diseases and conditions are commonly referred to as "orphan drugs";

(4) because so few individuals are affected by any one rare disease or condition, a pharmaceutical company which develops an orphan drug may reasonably expect the drug to generate relatively small sales in comparison to the cost of developing the drug and consequently to incur a financial loss;

(5) there is reason to believe that some promising orphan drugs will not be developed unless changes are made in the applicable Federal laws to reduce the costs of developing such drugs and to provide financial incentives to develop such drugs; and

(6) it is in the public interest to provide such changes and incentives for the development of orphan drugs.

Here is a link to the FDA site that explains a lot more about this subject:

http://www.fda.gov/forindustry/developingproductsforrarediseasesconditions/overview/ucm119477.htm

As you can see, Sapacitabine was granted Orphan Status for the treatment of myelodysplastic syndrome on June 24, 2010 and this is VERY GOOD news for CYCC...IMO

The image below is found here, and there is a daily chart that's showing a lot of improvement at the bottom of this post...Just take a look at the Volume that poured in when this news was discovered...I find it a bit unusual that the company has yet to put out a Press Release about this very positive development...I have sent an email to the Investors Relations representative at the company, and will post his reply when I get it...

http://www.accessdata.fda.gov/scripts/opdlisting/oopd/OOPD_Results_2.cfm?Index_Number=263408