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  2. Adalimumab - Wikipedia

    en.wikipedia.org/wiki/Adalimumab

    Adalimumab, sold under the brand name Humira and others, is a disease-modifying antirheumatic drug and monoclonal antibody used to treat rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, ulcerative colitis, plaque psoriasis, hidradenitis suppurativa, and uveitis.

  3. UnitedHealth to remove AbbVie's Humira from some US drug ...

    www.aol.com/news/unitedhealth-remove-abbvies...

    UnitedHealth said patients will have a way to get coverage for Humira until the preferred biosimilars on its plans are designated interchangeable by the U.S. Food and Drug Administration, meaning ...

  4. Patient portal - Wikipedia

    en.wikipedia.org/wiki/Patient_portal

    Some patient portal applications enable patients to register and complete forms online, which can streamline visits to clinics and hospitals. Many portal applications also enable patients to request prescription refills online, order eyeglasses and contact lenses, access medical records, pay bills, review lab results, and schedule medical ...

  5. Cambridge Antibody Technology - Wikipedia

    en.wikipedia.org/wiki/Cambridge_Antibody_Technology

    Humira, the brand name of adalimumab, is an anti-TNF antibody discovered by CAT as D2E7, then developed in the clinic and marketed by Abbvie, formerly Abbott Laboratories. CAT was also behind belimumab , the anti-BlyS antibody drug marketed as Benlysta and the first new approved drug for systemic lupus in more than 50 years. [ 1 ]

  6. No 8th Indication for You, Humira - AOL

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  7. What Are the Main Threats to AbbVie's Humira? - AOL

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  9. Filgotinib - Wikipedia

    en.wikipedia.org/wiki/Filgotinib

    [16] [full citation needed] Three groups of twelve patients were treated either with 200 mg filgotinib in a single dose, 200 mg divided in two doses or placebo. The primary end-point was the ACR20 score, which monitors improvements in the symptomatology of the patient. After the scheduled 4 weeks of treatment, 83% of the respondents showed an ...

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