CRWENewswire.com is pleased to announce a stock highlight on Celgene Corporation (Nasdaq: CELG), Monotype Imaging Holdings Inc. (Nasdaq: TYPE), Royale Energy Inc (NASDAQ:ROYL)

Celgene Corporation (Nasdaq: CELG) today August 5, 2009 announced that the National Comprehensive Cancer Network (NCCN) has updated its Clinical Practice Guidelines in Oncology™ v1.2010 and has upgraded VIDAZA® to a Category 1 recommended treatment for patients with intermediate-2 and high-risk myelodysplastic syndromes (MDS).

About VIDAZA® In December 2008, VIDAZA became the first and only drug approved by the European Commission to demonstrate a significant extension of overall survival compared to conventional care regimens, for patients with Intermediate-2 and high-risk MDS and AML

About Myelodysplastic Syndromes Myelodysplastic syndromes (MDS) are a group of hematologic malignancies that affect approximately 300,000 people worldwide. Myelodysplastic syndromes occur when blood cells remain in an immature or “blast” stage within the bone marrow and never develop into mature cells capable of performing their necessary functions.

Monotype

Below is a summary of updates to the BioMedReports.com database of over 200 entries included in the FDA and Clinical Trial Calendars. The FDA Calendar includes companies with pending new drug, biological agent, or medical device new product decisions at the FDA sorted by their PDUFA decision deadline dates while the Clinical Trial Calendar encompasses pending clinical trial results (with a focus on late-stage, Phase 3 trials), pending new submissions to the FDA (e.g. NDA, BLA, 510k, PMA, sNDA, sBLA filings), and pending re-submissions to the FDA for complete response rulings by the agency which require more information before an approval can be granted.

Allos Therapeutics [ALTH: 7.19, -0.13 (-1.78%)]: On 5/30/09 , ALTH updated data from the Company’s pivotal Phase 2 PROPEL study of pralatrexate in patients with relapsed or refractory peripheral T-cell lymphoma (PTCL). The overall response rate for pralatrexate as evaluated by central independent