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Investigator-Sponsored Phase 2 Study Results Show pSivida’s Medidur® Fully Controlled Uveitis for Two Years with No Recurrence of Disease While Visual Acuity Continued to Improve
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pSivida Announces Poster and Oral Presentation on Controlled Release of Avastin® from Tethadur™ Biodegradable Matrix at the 2016 Controlled Release Society Annual Meeting
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pSivida (PSDV) Completes Two Preclinical Studies Utilizing Durasert Technology
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pSivida Announces Successful Completion of Two Preclinical Studies of Durasert™ Sustained-Release Insert Delivering Repurposed Cancer Drug to Treat Wet AMD
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pSivida Corp. Provides Company Update and Reports Third Quarter FY 2016 Results
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pSivida CEO to Present at 2016 International Symposium of Ocular Pharmacology and Therapeutics
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pSivida's (PSDV) Medidur Granted Orphan Drug Designation in Europe as Uveitis Treatment
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pSivida’s Medidur for Posterior Uveitis Granted Orphan Drug Designation in Europe
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pSivida Corp. Announces Third Quarter Fiscal Year 2016 Financial Results Release Date and Conference Call Information
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pSivida to Present at the Sidoti Spring 2016 Emerging Growth Convention
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pSivida (PSDV) Announces Positive Six-Month Safety Data for Medidur Phase 3 in PU
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Additional Favorable Six-Month Safety Results for pSivida's Medidur™ for Posterior Uveitis
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pSivida Corp. Provides Company Update and Reports Second Quarter FY 2016 Results
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pSivida Corp Announces Second Quarter Fiscal Year 2016 Financial Results Release Date and Conference Call Information
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pSivida CEO to Present at 18th Annual Bio CEO & Investor Conference February 9
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pSivida (PSDV) Plans to File EU Marketing Approval for Medidur
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pSivida Plans Medidur™ EU Marketing Approval Application Based on Single Phase 3 Clinical Trial
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pSivida (PSDV) Announces Medidur Phase 3 Met Primary Efficacy Endpoint
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pSivida's Medidur™ Meets Primary Efficacy Endpoint in Phase 3 Trial: High Statistical Significance in Prevention of Recurrence of Posterior Uveitis (p Less Than 0.00000001)
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pSivida Corp. Provides Company Update and Reports First Quarter FY 2016 Results
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pSivida Corp Announces First Quarter FY 2016 Financial Results Release Date and Conference Call Information
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pSivida Announces NDA for Medidur™ Now Planned Using Six-Month Efficacy Data from Both Phase III Trials; FDA Concurs
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pSivida CEO to Present at Ladenburg Thalmann 2015 Healthcare Conference September 29, 2015
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pSivida Corp. Provides Company Update and Reports Fourth Quarter and FY 2015 Results
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pSivida CEO Invited to Speak at Surfaces in BioMaterials Foundation’s BioInterface 2015 Annual Symposium
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pSivida Corp Announces Fourth Quarter and Fiscal Year 2015 Financial Results Release Date and Conference Call Information
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pSivida CEO to Speak at Controlled Release Society Annual Meeting Workshop in Edinburgh, Scotland, This Weekend
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pSivida Announces Positive Top Line Results From Investigator-Sponsored Phase II Study of Medidur™ for Uveitis
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pSivida Announces Top-Line Results from Investigator-Sponsored Phase II Study of Medidur™ for Uveitis to Be Reported Next Week
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pSivida CEO to Present at ISOPT Clinical Meeting in Berlin in July 2015
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pSivida Reports Positive IOP Safety Data in Phase III Trial of Medidur™ for Posterior Uveitis
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pSivida Announces Two Tech Evaluation Agreements with Leading Global Pharmaceutical Company
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pSivida Corp. Reports Third Quarter FY 2015 Results
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pSivida Corp. Announces Third Quarter Fiscal Year 2015 Financial Results Release Date and Conference Call Information
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pSivida Corp. Reports ILUVIEN® for DME Approved in Poland
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pSivida Corp. Completes Targeted Enrollment of Phase III Trial of Medidur™ for Posterior Uveitis
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