pSivida Announces Resubmission of New Drug Application for Iluvien

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pSivida Announces Resubmission of New Drug Application for Iluvien

drugs.com

Iluvien (fluocinolone acetonide) is a new drug formulation in development for the treatment of Diabetic Macular Edema. Iluvien information includes news, clinical trial results and side effects.

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Tags: Edema, Diabetes, Drug, Clinical Trial, News

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Most Recently Shared on May 13, 2011 at 11:06 pm By:

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pSivida Announces Resubmission of New Drug Application for Iluvien: WATERTOWN, Mass.--(BUSINESS WIRE)--May... http://bit.ly/m19oHW #drug

1 year ago...

pSivida Announces Resubmission Of New Drug Application For ILUVIEN(R)

medicalnewstoday.com — “pSivida Corp. (NASDAQ: PSDV)(ASX: PVA), a leader in developing sustained release, drug delivery products for treatment of back-of-the-eye diseases, today announced that its licensee, Alimera ScienView full resource at medicalnewstoday.com

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Most Recently Shared on May 16, 2011 at 10:05 am By:

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pSivida Announces Resubmission Of New Drug Application For ILUVIEN(R) http://mnt.to/3VTh #diabetes

1 year ago...

Alimera receives FDA CRL for ILUVIEN NDA

news-medical.net — “pSivida Corp., a leader in developing sustained release, drug delivery products for treatment of back-of-the-eye diseases, including the investigational drug ILUVIEN® for the treatment of Diabetic Macular Edema (DME), today announced that Alimera Sciences, Inc, pSivida's collaborative partner, received a Complete Response Letter (CRL) from the U.S. Food and Drug Administration (FDA) regarding its New Drug Application (NDA) for ILUVIEN. The FDA issued the CRL to communicate its decision thatView full resource at news-medical.net

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Most Recently Shared on December 24, 2010 at 8:27 am By:

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Alimera receives FDA CRL for ILUVIEN NDA: pSivida Corp., a leader in developing sustained release, drug delivery... http://bit.ly/hnuJBP

1 year ago...

pSivida announces FDA Priority Review status for Iluvien NDA

news-medical.net — “pSivida Corp., a leader in the development of sustained release back of the eye drug delivery systems for difficult-to-treat conditions, today announced that its licensee, Alimera Sciences has been notified that the U.S. Food and Drug Administration (FDA) has granted Priority Review status for the New Drug Application (NDA) filed for Iluvien for the treatment diabetic macular edema (DME).View full resource at news-medical.net

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Most Recently Shared on August 31, 2010 at 1:26 pm By:

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pSivida announces FDA Priority Review status for Iluvien NDA: pSivida Corp., a leader in the development of sustai... http://bit.ly/8YNXRu

2 years ago...

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