<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14</volume><submitter>Allen-Philbey K</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To report on safety and effectiveness of subcutaneous cladribine (Litak&lt;sup>®&lt;/sup>) in multiple sclerosis (MS) patients.&lt;h4>Methods&lt;/h4>Litak&lt;sup>®&lt;/sup> was offered to MS-patients irrespective of disease course. Litak&lt;sup>®&lt;/sup> 10 mg was administered for 3-4 days during week 1. Based on lymphocyte count at week 4, patients received another 0-3 doses at week 5. A second course was administered 11 months later. Follow-up included adverse events, relapses, expanded disability status scale (EDSS), 9-hole-peg and Timed-25-foot-walking tests, no-evidence-of-disease-activity (NEDA), no-evidence-of-progression-or-active-disease (NEPAD), MRI, cerebrospinal fluid (CSF) neurofilament light chain (NfL), and lymphocyte counts.&lt;h4>Results&lt;/h4>In all, 208 patients received at least </pubmed_abstract><journal>Therapeutic advances in neurological disorders</journal><pagination>17562864211057661</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8842147</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Subcutaneous cladribine to treat multiple sclerosis: experience in 208 patients.</pubmed_title><pmcid>PMC8842147</pmcid><pubmed_authors>Giovannoni G</pubmed_authors><pubmed_authors>Constantinescu CS</pubmed_authors><pubmed_authors>Mattoscio M</pubmed_authors><pubmed_authors>Pavitt S</pubmed_authors><pubmed_authors>MacDougall A</pubmed_authors><pubmed_authors>Gran B</pubmed_authors><pubmed_authors>Ford H</pubmed_authors><pubmed_authors>Dalton C</pubmed_authors><pubmed_authors>Baker D</pubmed_authors><pubmed_authors>Blain C</pubmed_authors><pubmed_authors>Stennett A</pubmed_authors><pubmed_authors>Webb S</pubmed_authors><pubmed_authors>Juliusson G</pubmed_authors><pubmed_authors>Marta M</pubmed_authors><pubmed_authors>Sharrack B</pubmed_authors><pubmed_authors>Mao Z</pubmed_authors><pubmed_authors>Khaleeli Z</pubmed_authors><pubmed_authors>Peruzzotti-Jametti L</pubmed_authors><pubmed_authors>Alvarez-Gonzalez C</pubmed_authors><pubmed_authors>Chapman C</pubmed_authors><pubmed_authors>Adams A</pubmed_authors><pubmed_authors>Bianchi L</pubmed_authors><pubmed_authors>Chung K</pubmed_authors><pubmed_authors>Farrell RA</pubmed_authors><pubmed_authors>De Trane S</pubmed_authors><pubmed_authors>Fisniku L</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Schmierer K</pubmed_authors><pubmed_authors>Silber E</pubmed_authors><pubmed_authors>Turner BP</pubmed_authors><pubmed_authors>Mathews J</pubmed_authors><pubmed_authors>Scalfari A</pubmed_authors><pubmed_authors>Tallantyre EC</pubmed_authors><pubmed_authors>Gnanapavan S</pubmed_authors><pubmed_authors>Yildiz O</pubmed_authors><pubmed_authors>Hobart J</pubmed_authors><pubmed_authors>Pearson O</pubmed_authors><pubmed_authors>Allen-Philbey K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Subcutaneous cladribine to treat multiple sclerosis: experience in 208 patients.</name><description>&lt;h4>Objective&lt;/h4>To report on safety and effectiveness of subcutaneous cladribine (Litak&lt;sup>®&lt;/sup>) in multiple sclerosis (MS) patients.&lt;h4>Methods&lt;/h4>Litak&lt;sup>®&lt;/sup> was offered to MS-patients irrespective of disease course. Litak&lt;sup>®&lt;/sup> 10 mg was administered for 3-4 days during week 1. Based on lymphocyte count at week 4, patients received another 0-3 doses at week 5. A second course was administered 11 months later. Follow-up included adverse events, relapses, expanded disability status scale (EDSS), 9-hole-peg and Timed-25-foot-walking tests, no-evidence-of-disease-activity (NEDA), no-evidence-of-progression-or-active-disease (NEPAD), MRI, cerebrospinal fluid (CSF) neurofilament light chain (NfL), and lymphocyte counts.&lt;h4>Results&lt;/h4>In all, 208 patients received at least </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-06-01T02:33:10.949Z</modification><creation>2025-06-01T02:33:10.949Z</creation></dates><accession>S-EPMC8842147</accession><cross_references><pubmed>35173808</pubmed><doi>10.1177/17562864211057661</doi></cross_references></HashMap>