<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(1)</volume><submitter>Fain O</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Hereditary angioedema (HAE) is associated with a heavy burden of illness.&lt;h4>Objective&lt;/h4>To evaluate use of lanadelumab in a French Authorization for Temporary Use (ATU) program.&lt;h4>Methods&lt;/h4>ATU requests were made between October 12, 2018, and March 13, 2019; patients were followed through September 23, 2019. At entry, patients received lanadelumab 300 mg every 2 weeks. HAE attack characteristics were evaluated at day (D) 0 and months (M) 3 and 6. Patients completed the Angioedema Quality of Life (AE-QoL) questionnaire at initiation and monthly and the Angioedema Activity Score questionnaire daily in 28 day cycles (AAS28).&lt;h4>Results&lt;/h4>In total, 77 patients received ≥ 1 lanadelumab dose; 69 had ≥ 1 quarterly follow-up visit (analyzed population). Mean (standard de</pubmed_abstract><journal>Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology</journal><pagination>30</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8976389</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Long-term prophylaxis with lanadelumab for HAE: authorization for temporary use in France.</pubmed_title><pmcid>PMC8976389</pmcid><pubmed_authors>Boudjemia K</pubmed_authors><pubmed_authors>Launay D</pubmed_authors><pubmed_authors>Weiss L</pubmed_authors><pubmed_authors>Aubineau M</pubmed_authors><pubmed_authors>Fain O</pubmed_authors><pubmed_authors>Du-Thanh A</pubmed_authors><pubmed_authors>Gobert D</pubmed_authors><pubmed_authors>Inhaber N</pubmed_authors><pubmed_authors>Boccon-Gibod I</pubmed_authors><pubmed_authors>Bouillet L</pubmed_authors><pubmed_authors>Sobel A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long-term prophylaxis with lanadelumab for HAE: authorization for temporary use in France.</name><description>&lt;h4>Background&lt;/h4>Hereditary angioedema (HAE) is associated with a heavy burden of illness.&lt;h4>Objective&lt;/h4>To evaluate use of lanadelumab in a French Authorization for Temporary Use (ATU) program.&lt;h4>Methods&lt;/h4>ATU requests were made between October 12, 2018, and March 13, 2019; patients were followed through September 23, 2019. At entry, patients received lanadelumab 300 mg every 2 weeks. HAE attack characteristics were evaluated at day (D) 0 and months (M) 3 and 6. Patients completed the Angioedema Quality of Life (AE-QoL) questionnaire at initiation and monthly and the Angioedema Activity Score questionnaire daily in 28 day cycles (AAS28).&lt;h4>Results&lt;/h4>In total, 77 patients received ≥ 1 lanadelumab dose; 69 had ≥ 1 quarterly follow-up visit (analyzed population). Mean (standard de</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-06-01T02:44:09.335Z</modification><creation>2025-06-01T02:44:09.335Z</creation></dates><accession>S-EPMC8976389</accession><cross_references><pubmed>35365234</pubmed><doi>10.1186/s13223-022-00664-4</doi></cross_references></HashMap>