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  2. FDA gives emergency authorization to most precise ... - AOL

    www.aol.com/news/fda-gives-emergency...

    The test, which on Wednesday received emergency-use authorization from the U.S. Food and Drug Administration, measures the number of neutralizing antibodies that the body's immune system has ...

  3. 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This list of over 500 monoclonal antibodies includes approved and investigational drugs as well as drugs that have been withdrawn from market; consequently, the column Use does not necessarily indicate clinical usage.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.

  4. Some worry that the first FDA-approved at-home test for STIs ...

    www.aol.com/news/worry-first-fda-approved-home...

    The FDA's first-ever approval of an at-home test for chlamydia and ... The test kit, called Simple 2, does not screen for syphilis, which typically requires at least a finger-prick blood sample ...

  5. Infectious mononucleosis - Wikipedia

    en.wikipedia.org/wiki/Infectious_mononucleosis

    Antibody to EBNA slowly appears 2 to 4 months after the onset of symptoms and persists for the rest of a person’s life. [10] When negative, these tests are more accurate than the heterophile antibody test in ruling out infectious mononucleosis. When positive, they feature similar specificity to the heterophile antibody test.

  6. Tafasitamab - Wikipedia

    en.wikipedia.org/wiki/Tafasitamab

    Tafasitamab is a humanized Fc-modified cytolytic CD19 antibody. [5] [8] Tafasitamab was approved for medical use in the United States in July 2020, [7] [8] [9] and in the European Union in August 2021. [6] [10] The U.S. Food and Drug Administration (FDA) considers it to be a first-in-class medication. [11]

  7. FDA gives emergency authorization to most precise ... - AOL

    www.aol.com/fda-gives-emergency-authorization...

    The test, which on Wednesday received emergency-use authorization from the U.S. Food and Drug Administration (FDA), measures the number of neutralizing antibodies that the body’s immune system ...

  8. US FDA approves first at-home syphilis test - AOL

    www.aol.com/news/us-fda-approves-first-home...

    Developed by privately held NOWDiagnostics, the antibody test helps identify current or past infection and provides a result in about 15 minutes. However, the regulator added that the results from ...

  9. Tralokinumab - Wikipedia

    en.wikipedia.org/wiki/Tralokinumab

    Tralokinumab is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy. [5] [3]In the United States, tralokinumab is indicated for the treatment of moderate-to-severe atopic dermatitis in adults whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable.