California Society of Health-System Pharmacists(@CSHP_Official) 's Twitter Profile Photo

.U.S. FDA Approves First Interchangeable Biosimilars to Treat Macular Degeneration and Other Eye Conditions

The FDA approved two interchangeable biosimilars for aflibercept (Eylea) to treat macular degeneration and other eye conditions.

More: bit.ly/3WYQDF4

.@US_FDA Approves First Interchangeable Biosimilars to Treat Macular Degeneration and Other Eye Conditions

The FDA approved two interchangeable biosimilars for aflibercept (Eylea) to treat macular degeneration and other eye conditions.

More: bit.ly/3WYQDF4
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UpToDate(@UpToDate) 's Twitter Profile Photo

The U.S. FDA approved Yesafili (aflibercept-jbvf) and Opuviz (aflibercept-yszy) as biosimilars to Eylea (aflibercept). For all the latest , check out our drug referential resource: ow.ly/FK9W50RWH7F.

The @US_FDA approved Yesafili (aflibercept-jbvf) and Opuviz (aflibercept-yszy) as biosimilars to Eylea (aflibercept). For all the latest #DrugNews, check out our drug referential resource: ow.ly/FK9W50RWH7F.
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Modern Retina(@ModernRetina) 's Twitter Profile Photo

The Food and Drug Administration (FDA) announced its approval of 2 biosimilars as interchangeable with aflibercept 2 mg (Eylea). All 3 products are anti-VEGF agents, administered intravitreally for nAMD.

Read more: modernretina.com/view/us-fda-is…

The Food and Drug Administration (FDA) announced its approval of 2 biosimilars as interchangeable with aflibercept 2 mg (Eylea). All 3 products are anti-VEGF agents, administered intravitreally for nAMD. 

Read more: modernretina.com/view/us-fda-is…
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Arndt Vogel(@ArndtVogel) 's Twitter Profile Photo

🔥Maintenance with 5FU/LV-Aflibercept after FOLFIRI-Aflibercept vs treatment until progression in older pts in 2nd line mCRC:
✅ AFEMA trial, age >70 yrs
👉ORR 20 vs 9%
👉mPFS 6.1 vs 5.5 mo
👉mOS 12.2 vs 11.5 mo
🧐non-inferiority for PFS shown, ORR & OS did not differ,

🔥Maintenance with 5FU/LV-Aflibercept after FOLFIRI-Aflibercept vs treatment until progression in older pts in 2nd line mCRC: #ESMO23
✅ AFEMA trial, age >70 yrs
👉ORR 20 vs 9%
👉mPFS 6.1 vs 5.5 mo
👉mOS 12.2 vs 11.5 mo
🧐non-inferiority for PFS shown, ORR & OS did not differ,
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Ophthalmology Advisor(@ophth_advisor) 's Twitter Profile Photo

A (8 mg) delivered every 12 or 16 weeks is noninferior to the standard dosage of 2 mg delivered every 8 weeks for the treatment of (DME). Published in The Lancet

Read more: brnw.ch/21wJDf2

A #HighDoseAflibercept (8 mg) delivered every 12 or 16 weeks is noninferior to the standard #Aflibercept dosage of 2 mg delivered every 8 weeks for the treatment of #DiabeticMacularEdema (DME). Published in @TheLancet

Read more: brnw.ch/21wJDf2

#DME #Ophthalmology
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Ocular Surgery News(@Healio_OSN) 's Twitter Profile Photo

🚨 ICYMI 🚨

Mark R. Barakat, MD, discusses data on in patients receiving 8 mg for in the PHOTON trial compared with those receiving aflibercept 2 mg. 🎥👇
ARVO
healio.com/news/ophthalmo…

🚨 ICYMI 🚨 

Mark R. Barakat, MD, discusses data on #IOP in patients receiving #aflibercept 8 mg for #diabeticmacularedema in the PHOTON trial compared with those receiving aflibercept 2 mg. 🎥👇
#OcularSurgeryNews #glaucoma #ARVO2024 @ARVOinfo
healio.com/news/ophthalmo…
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Antonio(@AntonioRS5) 's Twitter Profile Photo

Cuando le digo a un paciente que tiene una DMAE exudativa y que le tengo que poner un Aflibercept Intravítreo

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Review of Optometry(@revoptom) 's Twitter Profile Photo

High-dose Aflibercept Pushes Dosing Interval to Five Months

Nearly half of subjects went 20 weeks or longer between injections with the 8mg formulation. The regimen also maintained BCVA gains out to 96 weeks.
reviewofoptometry.com/article/highdo…

High-dose Aflibercept Pushes Dosing Interval to Five Months

Nearly half of subjects went 20 weeks or longer between injections with the 8mg formulation. The regimen also maintained BCVA gains out to 96 weeks.
reviewofoptometry.com/article/highdo…
#eylea #amd #retina #eyecare #optometry
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Ophthalmology(@AAOjournal) 's Twitter Profile Photo

Similar risk of kidney failure among patients with blinding diseases who receive ranibizumab, aflibercept, and bevacizumab: an OHDSI Network Study
ow.ly/UitT50QYGkr

Similar risk of kidney failure among patients with blinding diseases who receive ranibizumab, aflibercept, and bevacizumab: an OHDSI Network Study
ow.ly/UitT50QYGkr
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Punit(@punitbansal14) 's Twitter Profile Photo

Aflibercept | Biosimilar | Patent Settlement

Biocon Biologics secures Canada market entry date for
Yesafili® (Aflibercept), a proposed biosimilar to Eylea

Ref: Biocon March'24

Aflibercept | Biosimilar | Patent Settlement

Biocon Biologics secures Canada market entry date for
Yesafili® (Aflibercept), a proposed biosimilar to Eylea

Ref: Biocon March'24
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Eyewire+(@eyewireplus) 's Twitter Profile Photo

Regeneron announced 1-year results from the pivotal PULSAR and PHOTON trials demonstrating Eylea HD (aflibercept injection 8 mg) extended dosing regimens were non-inferior to Eylea aflibercept injection 2 mg) for both the treatment of wet AMD and DME.

Regeneron announced 1-year results from the pivotal PULSAR and PHOTON trials demonstrating Eylea HD (aflibercept injection 8 mg) extended dosing regimens were non-inferior to Eylea aflibercept injection 2 mg) for both the treatment of wet AMD and DME.
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Biocon Biologics(@BioconBiologics) 's Twitter Profile Photo

Biocon Biologics Receives U.S. FDA Approval for Biosimilar Aflibercept for Yesafili. Enters U.S. Ophthalmology Market.

The U.S. Food and Drug Administration (US FDA) has approved Biocon Biologics first-to-file application for Yesafili (aflibercept-jbvf), an interchangeable

Biocon Biologics Receives U.S. FDA Approval for Biosimilar Aflibercept for Yesafili. Enters U.S. Ophthalmology Market.

The U.S. Food and Drug Administration (US FDA) has approved Biocon Biologics first-to-file application for Yesafili (aflibercept-jbvf), an interchangeable
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Modern Retina(@ModernRetina) 's Twitter Profile Photo

The Food and Drug Administration (FDA) announced its approval of 2 biosimilars as interchangeable with aflibercept 2 mg (Eylea). All 3 products are anti-VEGF agents, administered intravitreally for nAMD.

Read more: modernretina.com/view/us-fda-is…

The Food and Drug Administration (FDA) announced its approval of 2 biosimilars as interchangeable with aflibercept 2 mg (Eylea). All 3 products are anti-VEGF agents, administered intravitreally for nAMD. 

Read more: modernretina.com/view/us-fda-is…
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Ophthalmology Times(@OphthTimes) 's Twitter Profile Photo

The Kingfisher Study found that the visual outcomes after 1 year of brolucizumab, 6 mg, (Beovu, Novartis) in participants with diabetic macular edema (DME) did not differ significantly from those obtained with aflibercept

Read More: ophthalmologytimes.com/view/kingfishe…

The Kingfisher Study found that the visual outcomes after 1 year of brolucizumab, 6 mg, (Beovu, Novartis) in participants with diabetic macular edema (DME) did not differ significantly from those obtained with aflibercept

Read More: ophthalmologytimes.com/view/kingfishe…
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Ophthalmology(@AAOjournal) 's Twitter Profile Photo

Amongst patients with treatment-resistant nAMD, switching from aflibercept to faricimab may serve as a safe and effective option. Significant anatomical improvements were observed, with a trend towards visual stability. ow.ly/VMZ150Qf0hA

Amongst patients with treatment-resistant nAMD, switching from aflibercept to faricimab may serve as a safe and effective option. Significant anatomical improvements were observed, with a trend towards visual stability. ow.ly/VMZ150Qf0hA
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Ophthalmology Times(@OphthTimes) 's Twitter Profile Photo

Regeneron Pharmaceuticals announced the publication of one-year results from the pivotal PULSAR and PHOTON trials for aflibercept 8 mg injection (Eylea HD).

Read More: ow.ly/FU3K50QOXO5

Regeneron Pharmaceuticals announced the publication of one-year results from the pivotal PULSAR and PHOTON trials for aflibercept 8 mg injection (Eylea HD).

Read More: ow.ly/FU3K50QOXO5
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Optometry Times(@OptometryTimes) 's Twitter Profile Photo

Enrollment has now been completed for Opthea Limited’s COAST Phase 3 clinical trial, which is investigating the use of sozinibercept (OPT-302) and aflibercept for the treatment of wet age-related macular degeneration.

Read more: ow.ly/WqC950QFbfZ

Enrollment has now been completed for Opthea Limited’s COAST Phase 3 clinical trial, which is investigating the use of sozinibercept (OPT-302) and aflibercept for the treatment of wet age-related macular degeneration.

Read more: ow.ly/WqC950QFbfZ
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COFEPRIS(@COFEPRIS) 's Twitter Profile Photo

da a conocer el resultado del Comité de Moléculas Nuevas y del Subcomité de Evaluación de Productos Biotecnológicos sobre: Aflibercept recibiendo un resultado favorable 🧬

#CofeprisTransparente da a conocer el resultado del Comité de Moléculas Nuevas y del Subcomité de Evaluación de Productos Biotecnológicos sobre: Aflibercept recibiendo un resultado favorable 🧬
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Retina Today(@RetinaToday) 's Twitter Profile Photo

Prithu S. Mettu, MD, kicked off the sessions with a rundown of wet AMD therapies—new and still under investigation. Are you using faricimab or high-dose aflibercept yet? Duke Eye Center YoungMD Connect

Prithu S. Mettu, MD, kicked off the sessions with a rundown of wet AMD therapies—new and still under investigation. Are you using faricimab or high-dose aflibercept yet? #DukefAVS #retina @dukeeyecenter @YoungMDConnect
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