<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(1)</volume><submitter>Sanchez MF</submitter><funding>Ferring Pharmaceuticals, Denmark</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To explore the efficacy and safety of individualized follitropin delta dosing, based on serum anti-Müllerian hormone (AMH) concentration and bodyweight, in a long gonadotropin-releasing hormone (GnRH) agonist protocol.&lt;h4>Methods&lt;/h4>Clinical outcomes after one treatment cycle are reported in women with AMH: 5-35 pmol/L. Oocytes were inseminated by intracytoplasmic sperm injection, blastocyst transfer was on Day 5 and remaining blastocysts were cryopreserved. Data collection included live births and neonatal health follow-up for all fresh/frozen transfers performed within one year after treatment allocation.&lt;h4>Results&lt;/h4>In total, 104 women started stimulation, of whom 101 had oocyte recovery and 92 had blastocyst transfer. The average daily dose of follitropin delta was 11.0 ± 1.6 µg and the duration of stimulation was 10.3 ± 1.6 days. The mean number of oocytes was 12.5 ± 6.4, the mean number of blastocysts was 5.1 ± 3.4, and 85% had at least one good-quality blastocyst. Following mostly single blastocyst transfer (95%), the ongoing pregnancy rate was 43%, the live-birth rate was 43%, and the cumulative live-birth rate was 58% per started stimulation. There were 6 cases of early OHSS (5.8%) graded as mild (n = 3) and moderate (n = 3) and 6 cases of late OHSS (5.8%) graded as moderate (n = 3) and severe (n = 3).&lt;h4>Conclusion&lt;/h4>In this first evaluation of the individualized follitropin delta dosing in a long GnRH agonist protocol, the cumulative live-birth rate was high. A randomized trial comparing follitropin delta in a long GnRH agonist protocol versus in a GnRH antagonist protocol should provide further insight into the efficacy and safety of this treatment option.&lt;h4>Trial registration number&lt;/h4>NCT03564509; June 21, 2018.</pubmed_abstract><journal>Reproductive biology and endocrinology : RB&amp;E</journal><pagination>45</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10185461</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Live birth rates following individualized dosing algorithm of follitropin delta in a long GnRH agonist protocol.</pubmed_title><pmcid>PMC10185461</pmcid><pubmed_authors>Mannaerts B</pubmed_authors><pubmed_authors>Larsson P</pubmed_authors><pubmed_authors>Sanchez MF</pubmed_authors><pubmed_authors>Bosch E</pubmed_authors><pubmed_authors>Serrano MF</pubmed_authors><pubmed_authors>Velasco JAG</pubmed_authors><pubmed_authors>Lopez ES</pubmed_authors></additional><is_claimable>false</is_claimable><name>Live birth rates following individualized dosing algorithm of follitropin delta in a long GnRH agonist protocol.</name><description>&lt;h4>Purpose&lt;/h4>To explore the efficacy and safety of individualized follitropin delta dosing, based on serum anti-Müllerian hormone (AMH) concentration and bodyweight, in a long gonadotropin-releasing hormone (GnRH) agonist protocol.&lt;h4>Methods&lt;/h4>Clinical outcomes after one treatment cycle are reported in women with AMH: 5-35 pmol/L. Oocytes were inseminated by intracytoplasmic sperm injection, blastocyst transfer was on Day 5 and remaining blastocysts were cryopreserved. Data collection included live births and neonatal health follow-up for all fresh/frozen transfers performed within one year after treatment allocation.&lt;h4>Results&lt;/h4>In total, 104 women started stimulation, of whom 101 had oocyte recovery and 92 had blastocyst transfer. The average daily dose of follitropin delta was 11.0 ± 1.6 µg and the duration of stimulation was 10.3 ± 1.6 days. The mean number of oocytes was 12.5 ± 6.4, the mean number of blastocysts was 5.1 ± 3.4, and 85% had at least one good-quality blastocyst. Following mostly single blastocyst transfer (95%), the ongoing pregnancy rate was 43%, the live-birth rate was 43%, and the cumulative live-birth rate was 58% per started stimulation. There were 6 cases of early OHSS (5.8%) graded as mild (n = 3) and moderate (n = 3) and 6 cases of late OHSS (5.8%) graded as moderate (n = 3) and severe (n = 3).&lt;h4>Conclusion&lt;/h4>In this first evaluation of the individualized follitropin delta dosing in a long GnRH agonist protocol, the cumulative live-birth rate was high. A randomized trial comparing follitropin delta in a long GnRH agonist protocol versus in a GnRH antagonist protocol should provide further insight into the efficacy and safety of this treatment option.&lt;h4>Trial registration number&lt;/h4>NCT03564509; June 21, 2018.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-04T10:19:43.976Z</modification><creation>2025-02-19T00:12:37.729Z</creation></dates><accession>S-EPMC10185461</accession><cross_references><pubmed>37194068</pubmed><doi>10.1186/s12958-023-01090-w</doi></cross_references></HashMap>