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  2. Faricimab - Wikipedia

    en.wikipedia.org/wiki/Faricimab

    Faricimab, sold under the brand name Vabysmo (/ v ə ˈ b aɪ z m oʊ / və-BYEZ-mow), is a monoclonal antibody used for the treatment of neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME).

  3. FDA Approves First Injectable Eye Medicine For Vision Loss ...

    www.aol.com/news/fda-approves-first-injectable...

    Vabysmo is the first and only FDA-approved injectable eye medicine for wet AMD and DME that improves and. The FDA has approved Genentech's, a unit of Roche Holdings AG (OTC: RHHBY), Vabysmo ...

  4. List of therapeutic monoclonal antibodies - Wikipedia

    en.wikipedia.org/wiki/List_of_therapeutic...

    This list of over 500 monoclonal antibodies includes approved and investigational drugs as well as drugs that have been withdrawn from market; consequently, the column Use does not necessarily indicate clinical usage. See the list of FDA-approved therapeutic monoclonal antibodies in the monoclonal antibody therapy page.

  5. Regeneron's Eylea could return to growth after nod to high ...

    www.aol.com/news/regenerons-eylea-could-return...

    A longer dosing gap for the drug could help Regeneron take on rival Roche's Vabysmo and also help soften the blow from incoming cheaper copycat drugs, analysts said. Shares of Regeneron rose 1.7% ...

  6. Brolucizumab - Wikipedia

    en.wikipedia.org/wiki/Brolucizumab

    Brolucizumab is approved by the US Food and Drug Administration (FDA) for use in ophthalmology. [7] [8]Brolucizumab successfully completed phase III development in wet age-related macular degeneration (AMD) meeting the primary efficacy endpoint of non-inferiority to aflibercept in mean change in best corrected visual acuity (BCVA) from baseline to week 48.

  7. Inebilizumab - Wikipedia

    en.wikipedia.org/wiki/Inebilizumab

    Inebilizumab was approved for medical use in the United States in June 2020, [8] [10] in the European Union in April 2022, [7] and in Canada in December 2023. [1] The U.S. Food and Drug Administration (FDA) considers it to be a first-in-class medication .

  8. Roche shares fall on modest 2024 outlook - AOL

    www.aol.com/news/roche-forecasts-return-growth...

    LONDON/FRANKFURT (Reuters) -Roche shares fell more than 4% on Thursday as the market expressed disappointed with the company's more modest than expected 2024 outlook. Sales in 2023 rose 1% when ...

  9. Ravulizumab - Wikipedia

    en.wikipedia.org/wiki/Ravulizumab

    Ravulizumab was approved by the US Food and Drug Administration (FDA) in December 2018. [12] In April 2019, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended the granting of a conditional marketing authorization for ravulizumab. [13] Ravulizumab was approved for medical use in the EU in ...