PMID- 38361080 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240322 IS - 2193-8253 (Print) IS - 2193-6536 (Electronic) IS - 2193-6536 (Linking) VI - 13 IP - 2 DP - 2024 Apr TI - Safety and Tolerability of Combining CGRP Monoclonal Antibodies with Gepants in Patients with Migraine: A Retrospective Study. PG - 465-473 LID - 10.1007/s40120-024-00586-w [doi] AB - INTRODUCTION: The introduction of clacitonin gene-related peptide (CGRP) monoclonal antibodies (mAbs) has revolutionized the treatment of migraines. In clinical practice gepants might be considered as a valid option to treat acute attacks in patients with migraine who are treated with mAbs. However, the safety and tolerability of such a combination is not well addressed in the real-world setting. We designed this study to evaluate the safety and tolerability of combining CGRP mAbs with gepants in the management of migraines. METHODS: This was a retrospective, real-world, exploratory study. The participants included within the study were adult (>/= 18 years) patients diagnosed with migraine. Screening for patients who were treated with at least one GCRP mAbs was done. Data was collected from one site, the American Center for Psychiatry and Neurology, Abu Dhabi UAE. A total of 516 patients taking CGRP mAbs were identified. Extracted data from patients' electronic medical records included patient demographics, migraine characteristics, prescribed treatments, and adverse events (AEs). The tolerability and safety of the combination therapy was evaluated on the basis of documented AEs. RESULTS: Among the identified 516 patients, 234 were administered gepants in addition to the CRGP mAb (215, rimegepant; 19, ubrogepant). Eleven of the 234 patients switched from rimegepant to urogepant as a result of lack of efficacy; one patient switched from urogepant to zolmitriptan because of the lack of insurance coverage of the former medication. Among all the patients included in this study, three AEs were documented. These AEs were generally mild and transient and hence did not lead to discontinuation of treatment. Moreover, 42 of the 234 (17.9%) patients were switched from one class of CGRP mAbs to another at least once while continuing treatment with the assigned gepants. CONCLUSION: The findings of this study demonstrate that combining CGRP mAbs with gepants is a safe and well-tolerated treatment approach for migraine. Future studies are warranted to further validate these findings and explore long-term outcomes. CI - (c) 2024. The Author(s). FAU - Alsaadi, Taoufik AU - Alsaadi T AUID- ORCID: 0000-0002-7513-5706 AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. talsaadi@live.ca. FAU - Suliman, Reem AU - Suliman R AUID- ORCID: 0009-0002-9607-3353 AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. Rk.suliman16@gmail.com. FAU - Santos, Vanessa AU - Santos V AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. FAU - Al Qaisi, Ibrahim AU - Al Qaisi I AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. FAU - Carmina, Princess AU - Carmina P AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. FAU - Aldaher, Batool AU - Aldaher B AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. FAU - Haddad, Shadi AU - Haddad S AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. FAU - Bader, Yazan AU - Bader Y AD - Department of Neurology, American Center for Psychiatry and Neurology, Abu Dhabi, UAE. LA - eng PT - Journal Article DEP - 20240215 PL - New Zealand TA - Neurol Ther JT - Neurology and therapy JID - 101637818 PMC - PMC10951184 OTO - NOTNLM OT - CGRP mAbs OT - Eptinezumab OT - Erenumab OT - Gepants OT - Migraine OT - Safety OT - Tolerability OT - UAE COIS- Batool Al Daher, Ibrahim Al Qaisi, Princess Carmina, Reem Suliman, Shadi Haddad, Taoufik AlSaadi, and Yazan Bader have no competing interests and nothing to disclose. EDAT- 2024/02/16 06:43 MHDA- 2024/02/16 06:44 PMCR- 2024/02/15 CRDT- 2024/02/16 00:03 PHST- 2023/12/25 00:00 [received] PHST- 2024/01/29 00:00 [accepted] PHST- 2024/02/16 06:44 [medline] PHST- 2024/02/16 06:43 [pubmed] PHST- 2024/02/16 00:03 [entrez] PHST- 2024/02/15 00:00 [pmc-release] AID - 10.1007/s40120-024-00586-w [pii] AID - 586 [pii] AID - 10.1007/s40120-024-00586-w [doi] PST - ppublish SO - Neurol Ther. 2024 Apr;13(2):465-473. doi: 10.1007/s40120-024-00586-w. Epub 2024 Feb 15.