FDA rejection raises serious questions for Momenta
The fallout over the FDA's rejection of Momenta's generic version of Lovenox--a rare setback for any developer--is continuing to dent the drug developer's reputation. Analysts have zeroed in on the implications the rejection has for Momenta's whole approach to development. As Cowen & Co. analyst Eric Schmidt noted, "We expect investors to be skeptical around Momenta's entire technology platform, pipeline and complex generic strategy." Ouch.
- read the report from The Wall Street Journal
- take a look at yesterday's release on the rejection
Related Articles:
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Sanofi loses Lovenox patent protection. Report
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Lovenox reduces cardio risks but can cause bleeding. Report


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