<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(1)</volume><submitter>Gantenbein AR</submitter><funding>Novartis Pharma Schweiz AG</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>The fully human monoclonal antibody erenumab, which targets the calcitonin gene-related peptide (CGRP) receptor, was licensed in Switzerland in July 2018 for the prophylactic treatment of migraine. To complement findings from the pivotal program, this observational study was designed to collect and evaluate clinical data on the impact of erenumab on several endpoints, such as quality of life, migraine-related impairment and treatment satisfaction in a real-world setting.&lt;h4>Methods&lt;/h4>An interim analysis was conducted after all patients completed 6 months of erenumab treatment. Patients kept a headache diary and completed questionnaires at follow up visits. The overall study duration comprises 24 months.&lt;h4>Results&lt;/h4>In total, 172 adults with chronic or episodic migra</pubmed_abstract><journal>The journal of headache and pain</journal><pagination>142</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9673191</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Swiss QUality of life and healthcare impact Assessment in a Real-world Erenumab treated migraine population (SQUARE study): interim results.</pubmed_title><pmcid>PMC9673191</pmcid><pubmed_authors>Ryvlin P</pubmed_authors><pubmed_authors>Arzt ME</pubmed_authors><pubmed_authors>Meyer I</pubmed_authors><pubmed_authors>Petersen JA</pubmed_authors><pubmed_authors>Gantenbein AR</pubmed_authors><pubmed_authors>Landmann G</pubmed_authors><pubmed_authors>Viceic D</pubmed_authors><pubmed_authors>Schafer E</pubmed_authors><pubmed_authors>Agosti R</pubmed_authors><pubmed_authors>Zecca C</pubmed_authors><pubmed_authors>Schankin CJ</pubmed_authors><pubmed_authors>Pohl H</pubmed_authors><pubmed_authors>Kamm CP</pubmed_authors><pubmed_authors>Meier N</pubmed_authors><pubmed_authors>Merki-Feld GS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Swiss QUality of life and healthcare impact Assessment in a Real-world Erenumab treated migraine population (SQUARE study): interim results.</name><description>&lt;h4>Background&lt;/h4>The fully human monoclonal antibody erenumab, which targets the calcitonin gene-related peptide (CGRP) receptor, was licensed in Switzerland in July 2018 for the prophylactic treatment of migraine. To complement findings from the pivotal program, this observational study was designed to collect and evaluate clinical data on the impact of erenumab on several endpoints, such as quality of life, migraine-related impairment and treatment satisfaction in a real-world setting.&lt;h4>Methods&lt;/h4>An interim analysis was conducted after all patients completed 6 months of erenumab treatment. Patients kept a headache diary and completed questionnaires at follow up visits. The overall study duration comprises 24 months.&lt;h4>Results&lt;/h4>In total, 172 adults with chronic or episodic migra</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T08:08:51.021Z</modification><creation>2025-02-19T01:56:44.01Z</creation></dates><accession>S-EPMC9673191</accession><cross_references><pubmed>36401172</pubmed><doi>10.1186/s10194-022-01515-8</doi></cross_references></HashMap>