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  2. Ruxolitinib - Wikipedia

    en.wikipedia.org/wiki/Ruxolitinib

    Ruxolitinib (sold under the brand names Jakafi and Jakavi among others, and as Opzelura in cream form) is a medication used for the treatment of intermediate or high-risk myelofibrosis, [6] a type of myeloproliferative neoplasm that affects the bone marrow; [11] [12] polycythemia vera, when there has been an inadequate response to or intolerance of hydroxyurea; [6] [13] and steroid-refractory ...

  3. Deuruxolitinib - Wikipedia

    en.wikipedia.org/wiki/Deuruxolitinib

    Deuruxolitinib, sold under the brand name Leqselvi, is a medication used for the treatment of alopecia areata. [1] It is a Janus kinase inhibitor selective for JAK1 and JAK2. [2]

  4. REACH authorisation procedure - Wikipedia

    en.wikipedia.org/wiki/REACh_authorisation_procedure

    The formulation of a mixture is considered as a use under REACh and the substance of the Annex XIV is only subject to authorisation if it exceeds the required concentrations. If the production of an article may require an authorisation at some point, finished articles themselves do not require an authorisation to be put on the market, even ...

  5. Baricitinib - Wikipedia

    en.wikipedia.org/wiki/Baricitinib

    It reaches highest blood plasma levels after about an hour; in different individuals the time to reach this level ranges from 0.5 to 3 hours. Food intake has no relevant influence on the drug's pharmacokinetics. 50% of the circulating baricitinib are bound to blood plasma proteins .

  6. Rociletinib - Wikipedia

    en.wikipedia.org/wiki/Rociletinib

    Rociletinib is a medication developed to treat non-small cell lung carcinomas with a specific mutation. It is a third-generation epidermal growth factor receptor tyrosine kinase inhibitor. [1]

  7. Pelabresib - Wikipedia

    en.wikipedia.org/wiki/Pelabresib

    A phase one study of pelabresib in patients with relapsed/refractory lymphomas found pelabresib is capable of BET target gene suppression in an exposure-dependent manner with an acceptable safety profile leading to the recommended phase II dose of the 125 mg tablet once daily.

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