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Novartis Pharma AG: Novartis Phase III Beovu data show potential for fluid resolution in more diabetic macular edema patients with fewer injections versus aflibercept


Novartis Pharma AG: Novartis Phase III Beovu data show potential for fluid resolution in more diabetic macular edema patients with fewer injections versus aflibercept
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More patients treated with Beovu 6 mg experienced fluid (IRF/SRF) resolution at week 32 and week 52 versus aflibercept; fluid is a key marker of disease activity in DME
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Phase III KESTREL and KITE trials are the first pivotal trials to assess an anti-VEGF on six-week dosing intervals in the loading phase, suggesting Beovu may offer fewer injections from the start of treatment
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Novartis is committed to bringing Beovu 6 mg to DME patients and will submit data from KESTREL and KITE to global health authorities in H1 2021 ....

United Kingdom , United States , Isabella Zinck , Eylea Tarrytown , Thomas Hungerbuehler , Davidm Brown , Amy Wolf , Samir Shah , Jill Hopkins , Julie Masow , Beovu Basel , Sloan Simpson , Novartis Division Communications , Novartis External Communications , National Eye Institute , National Health Insurance Pricing , Novartis Pharmaceuticals , Global Development Unit Head , Clinical Research , Technologies In Health , Kite Pharma Inc , Regeneron Pharmaceuticals Inc , Canadian Drug Expert Committee Recommendation , Exchange Commission , Canadian Agency For Drugs , Association For Research ,

Investegate |NOVARTIS AG CHF0.50(REGD) Announcements | NOVARTIS AG CHF0.50(REGD): Novartis Phase III Beovu® data show potential for fluid resolution in more diabetic macular edema patients with fewer injections versus aflibercept


NOVARTIS AG CHF0.50(REGD)
Novartis Phase III Beovu® data show potential for fluid resolution in more diabetic macular edema patients with fewer injections versus aflibercept
Novartis Phase III Beovu® data show potential for fluid resolution in more diabetic macular edema patients with fewer injections versus aflibercept
In KESTREL and KITE, Beovu (brolucizumab) 6 mg met the primary endpoints of non-inferiority in change in best corrected visual acuity from baseline versus aflibercept 2 mg at year one in diabetic macular edema (DME) patients
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More patients treated with Beovu 6 mg experienced fluid (IRF/SRF) resolution at week 32 and week 52 versus aflibercept; fluid is a key marker of disease activity in DME ....

United Kingdom , United States , Isabella Zinck , Eylea Tarrytown , Thomas Hungerbuehler , Davidm Brown , Amy Wolf , Samir Shah , Jill Hopkins , Julie Masow , Beovu Basel , Sloan Simpson , Novartis Division Communications , Novartis External Communications , National Eye Institute , National Health Insurance Pricing , Novartis Pharmaceuticals , Global Development Unit Head , Clinical Research , Technologies In Health , Kite Pharma Inc , Regeneron Pharmaceuticals Inc , Canadian Drug Expert Committee Recommendation , Exchange Commission , Canadian Agency For Drugs , Association For Research ,