<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chan A</submitter><funding>NIAID NIH HHS</funding><pagination>510-519</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7837440</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(6)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Delayed-release dimethyl fumarate (DMF) has demonstrated robust efficacy in treating patients with relapsing-remitting multiple sclerosis. Decreases in absolute lymphocyte count (ALC) are a well-known pharmacodynamic effect of DMF treatment, but lymphocyte recovery dynamics are not well characterized after discontinuation of DMF.&lt;h4>Methods&lt;/h4>Data sources included the Biogen DMF integrated clinical trial data set, a retrospective US chart abstraction study, and data from MSBase. We assessed rate and time course of lymphocyte reconstitution after DMF discontinuation.&lt;h4>Results&lt;/h4>The majority of patients who developed lymphopenia while treated with DMF and subsequently discontinued treatment experienced ALC reconstitution. The median time to reach ALC ≥0.8 × 10&lt;sup>9&lt;</pubmed_abstract><journal>Neurology. Clinical practice</journal><pubmed_title>Lymphocyte reconstitution after DMF discontinuation in clinical trial and real-world patients with MS.</pubmed_title><pmcid>PMC7837440</pmcid><funding_grant_id>UM1 AI144288</funding_grant_id><pubmed_authors>Gold R</pubmed_authors><pubmed_authors>Wright K</pubmed_authors><pubmed_authors>Rose J</pubmed_authors><pubmed_authors>Kalincik T</pubmed_authors><pubmed_authors>Chan A</pubmed_authors><pubmed_authors>Spelman T</pubmed_authors><pubmed_authors>Ferraro D</pubmed_authors><pubmed_authors>Alvarez E</pubmed_authors><pubmed_authors>Bar-Or A</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Fam S</pubmed_authors><pubmed_authors>Wu F</pubmed_authors><pubmed_authors>Fox RJ</pubmed_authors><pubmed_authors>Butzkueven H</pubmed_authors><pubmed_authors>Sola P</pubmed_authors><pubmed_authors>McGuigan C</pubmed_authors><pubmed_authors>Lechner-Scott J</pubmed_authors><pubmed_authors>Haartsen J</pubmed_authors><pubmed_authors>Miller C</pubmed_authors><pubmed_authors>Gudesblatt M</pubmed_authors><pubmed_authors>Hodgkinson S</pubmed_authors><pubmed_authors>Spach K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lymphocyte reconstitution after DMF discontinuation in clinical trial and real-world patients with MS.</name><description>&lt;h4>Background&lt;/h4>Delayed-release dimethyl fumarate (DMF) has demonstrated robust efficacy in treating patients with relapsing-remitting multiple sclerosis. Decreases in absolute lymphocyte count (ALC) are a well-known pharmacodynamic effect of DMF treatment, but lymphocyte recovery dynamics are not well characterized after discontinuation of DMF.&lt;h4>Methods&lt;/h4>Data sources included the Biogen DMF integrated clinical trial data set, a retrospective US chart abstraction study, and data from MSBase. We assessed rate and time course of lymphocyte reconstitution after DMF discontinuation.&lt;h4>Results&lt;/h4>The majority of patients who developed lymphopenia while treated with DMF and subsequently discontinued treatment experienced ALC reconstitution. The median time to reach ALC ≥0.8 × 10&lt;sup>9&lt;</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2025-04-04T13:04:45.083Z</modification><creation>2021-02-21T05:04:51Z</creation></dates><accession>S-EPMC7837440</accession><cross_references><pubmed>33510947</pubmed><doi>10.1212/CPJ.0000000000000800</doi></cross_references></HashMap>