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Investegate |NOVARTIS AG CHF0.50(REGD) Announcements | NOVARTIS AG CHF0.50(REGD): Novartis reports one year results of Phase III MERLIN study evaluating Beovu® every four week dosing and provides update on Beovu clinical program


NOVARTIS AG CHF0.50(REGD)
Novartis reports one year results of Phase III MERLIN study evaluating Beovu® every four week dosing and provides update on Beovu clinical program
Novartis reports one year results of Phase III MERLIN study evaluating Beovu® every four week dosing and provides update on Beovu clinical program
Beovu (brolucizumab) met MERLIN’s primary endpoint of non-inferiority in change in best corrected visual acuity from baseline and superiority on anatomical secondary endpoints at year one versus aflibercept when given every four weeks following the loading phase
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In this study evaluating every four week dosing, Beovu was associated with higher rates of IOI including retinal vasculitis and retinal vascular occlusion versus aflibercept ....

United States , United Kingdom , Isabella Zinck , Rachel Fink , Lookeren Campagne , Thomas Hungerbuehler , Amy Wolf , Samir Shah , Julie Masow , Beovu Basel , Sloan Simpson , John Tsai , Novartis Division Communications , World Health Organization , Global Head Of Drug Development , Novartis External Communications , Health Qual Life Outcomes , Exchange Commission , Canadian Drug Expert Committee Recommendation , National Eye Institute , National Health Insurance Pricing , European Society Of Retina Specialists , Canadian Agency For Drugs , Technologies In Health , Lancet Glob Health , Global Head ,

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
1
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 ,

Novartis International AG: Novartis reports positive topline results from second Phase III trial of Beovu in patients with diabetic macular edema


Novartis International AG: Novartis reports positive topline results from second Phase III trial of Beovu in patients with diabetic macular edema
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Beovu (brolucizumab 6 mg) achieved its primary endpoint of non-inferiority to aflibercept 2 mg in change in best-corrected visual acuity (BCVA) at year one (week 52)
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In a secondary endpoint, more than half of Beovu patients in the 6 mg arm were maintained on a three-month dosing interval through year one, following the loading phase
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Significant improvement with Beovu 6 mg in change of central subfield thickness (CST) from baseline over the period of week 40 through week 52 was observed
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Novartis intends to submit the data from KESTREL, together with the data from the pivotal Phase III KITE ....

United States , Eric Althoff , Isabella Zinck , Dirk Sauer , Thomas Hungerbuehler , Amy Wolf , Indianj Ophthalmol , Samir Shah , Beovu Basel , Sloan Simpson , Kite Pharma Inc , Novartis Division Communications , Novartis Us External Communications , Novartis External Communications , Exchange Commission , Canadian Drug Expert Committee Recommendation , Global Head Development , National Eye Institute , National Health Insurance Pricing , Canadian Agency For Drugs , Technologies In Health , Association For Research , Novartis Pharma , Kite Pharma , Patients With Visual Impairment Due , Diabetic Macular Edema ,