Effects of the Oral Oxytocin Receptor Antagonist Tocolytic OBE001 on Reproduction in Rats
Background: OBE001 is a novel, orally active nonpeptide oxytocin receptor antagonist under development for the treatment of preterm labor and improvement in embryo implantation and pregnancy rate in assisted reproductive technology (ART). The reproductive safety of OBE001 was evaluated in customized...
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Veröffentlicht in: | Reproductive sciences (Thousand Oaks, Calif.) Calif.), 2016-04, Vol.23 (4), p.439-447 |
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creator | Pohl, Oliver Perks, Deborah Rhodes, Jon Comotto, Laura Baldrick, Paul Chollet, André |
description | Background:
OBE001 is a novel, orally active nonpeptide oxytocin receptor antagonist under development for the treatment of preterm labor and improvement in embryo implantation and pregnancy rate in assisted reproductive technology (ART). The reproductive safety of OBE001 was evaluated in customized fertility embryonic development (FER)/early embryonic development (EED) and fetal development (FD) and pre/postnatal development (PPN) studies mimicking clinical exposure scenarios.
Methods:
Oral OBE001 was evaluated at doses of 37.5, 75, and 125 mg/kg/d in female rats during a FER/EED study (from premating to implantation) and throughout FD during a FD/PPN study.
Results:
No OBE001 effects were observed during the FER/EED study. The FD/PPN study did not result in adverse OBE001 effects in females allowed to litter, their offspring, and second-generation fetuses. Females at 125 mg/kg/d who underwent cesarean section before term had slight reductions in body weights and food consumption, and associated fetuses had slightly delayed ossification of skull bones, which was not adverse in the absence of effects on live offspring.
Conclusion:
OBE001 at up to 125 mg/kg/d had no effects on EED and no adverse effects on FD and postnatal development of rats. These results constitute an important step toward the development of OBE001 in preterm labor and ART indications. |
doi_str_mv | 10.1177/1933719115607979 |
format | Article |
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OBE001 is a novel, orally active nonpeptide oxytocin receptor antagonist under development for the treatment of preterm labor and improvement in embryo implantation and pregnancy rate in assisted reproductive technology (ART). The reproductive safety of OBE001 was evaluated in customized fertility embryonic development (FER)/early embryonic development (EED) and fetal development (FD) and pre/postnatal development (PPN) studies mimicking clinical exposure scenarios.
Methods:
Oral OBE001 was evaluated at doses of 37.5, 75, and 125 mg/kg/d in female rats during a FER/EED study (from premating to implantation) and throughout FD during a FD/PPN study.
Results:
No OBE001 effects were observed during the FER/EED study. The FD/PPN study did not result in adverse OBE001 effects in females allowed to litter, their offspring, and second-generation fetuses. Females at 125 mg/kg/d who underwent cesarean section before term had slight reductions in body weights and food consumption, and associated fetuses had slightly delayed ossification of skull bones, which was not adverse in the absence of effects on live offspring.
Conclusion:
OBE001 at up to 125 mg/kg/d had no effects on EED and no adverse effects on FD and postnatal development of rats. These results constitute an important step toward the development of OBE001 in preterm labor and ART indications.</description><identifier>ISSN: 1933-7191</identifier><identifier>EISSN: 1933-7205</identifier><identifier>DOI: 10.1177/1933719115607979</identifier><identifier>PMID: 26399985</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Administration, Oral ; Animals ; Embryology ; Female ; Male ; Medicine & Public Health ; Obstetrics/Perinatology/Midwifery ; Original Article ; Oximes - administration & dosage ; Pregnancy ; Pyrrolidines - administration & dosage ; Rats ; Rats, Sprague-Dawley ; Receptors, Oxytocin - antagonists & inhibitors ; Receptors, Oxytocin - physiology ; Reproduction - drug effects ; Reproduction - physiology ; Reproductive Medicine ; Tocolytic Agents - administration & dosage</subject><ispartof>Reproductive sciences (Thousand Oaks, Calif.), 2016-04, Vol.23 (4), p.439-447</ispartof><rights>The Author(s) 2015</rights><rights>Society for Reproductive Investigation 2015</rights><rights>The Author(s) 2015.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-2f304906a2d572aeae9f686907d4c87176bbd847b66526d2757e19f060ae451c3</citedby><cites>FETCH-LOGICAL-c421t-2f304906a2d572aeae9f686907d4c87176bbd847b66526d2757e19f060ae451c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1933719115607979$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1933719115607979$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,41464,42533,43597,43598,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26399985$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pohl, Oliver</creatorcontrib><creatorcontrib>Perks, Deborah</creatorcontrib><creatorcontrib>Rhodes, Jon</creatorcontrib><creatorcontrib>Comotto, Laura</creatorcontrib><creatorcontrib>Baldrick, Paul</creatorcontrib><creatorcontrib>Chollet, André</creatorcontrib><title>Effects of the Oral Oxytocin Receptor Antagonist Tocolytic OBE001 on Reproduction in Rats</title><title>Reproductive sciences (Thousand Oaks, Calif.)</title><addtitle>Reprod. Sci</addtitle><addtitle>Reprod Sci</addtitle><description>Background:
OBE001 is a novel, orally active nonpeptide oxytocin receptor antagonist under development for the treatment of preterm labor and improvement in embryo implantation and pregnancy rate in assisted reproductive technology (ART). The reproductive safety of OBE001 was evaluated in customized fertility embryonic development (FER)/early embryonic development (EED) and fetal development (FD) and pre/postnatal development (PPN) studies mimicking clinical exposure scenarios.
Methods:
Oral OBE001 was evaluated at doses of 37.5, 75, and 125 mg/kg/d in female rats during a FER/EED study (from premating to implantation) and throughout FD during a FD/PPN study.
Results:
No OBE001 effects were observed during the FER/EED study. The FD/PPN study did not result in adverse OBE001 effects in females allowed to litter, their offspring, and second-generation fetuses. Females at 125 mg/kg/d who underwent cesarean section before term had slight reductions in body weights and food consumption, and associated fetuses had slightly delayed ossification of skull bones, which was not adverse in the absence of effects on live offspring.
Conclusion:
OBE001 at up to 125 mg/kg/d had no effects on EED and no adverse effects on FD and postnatal development of rats. These results constitute an important step toward the development of OBE001 in preterm labor and ART indications.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Embryology</subject><subject>Female</subject><subject>Male</subject><subject>Medicine & Public Health</subject><subject>Obstetrics/Perinatology/Midwifery</subject><subject>Original Article</subject><subject>Oximes - administration & dosage</subject><subject>Pregnancy</subject><subject>Pyrrolidines - administration & dosage</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Oxytocin - antagonists & inhibitors</subject><subject>Receptors, Oxytocin - physiology</subject><subject>Reproduction - drug effects</subject><subject>Reproduction - physiology</subject><subject>Reproductive Medicine</subject><subject>Tocolytic Agents - administration & dosage</subject><issn>1933-7191</issn><issn>1933-7205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM9PwyAcxYnRuDm9ezIcvVSBFijHucwfyZImZh48NZTC7NKVCTRx_7002zx4MJ6A7_u8ly8PgGuM7jDm_B6LNOVYYEwZ4oKLEzAeRgkniJ4e71EfgQvv1wjRTJD8HIwIS4UQOR2D97kxWgUPrYHhQ8PCyRYWX7tgVdPBV630NlgHp12QK9s1PsClVbbdhUbB4mGOEIZ24LbO1r0KTXwMPhn8JTgzsvX66nBOwNvjfDl7ThbF08tsukhURnBIiElRJhCTpKacSC21MCxnAvE6UznHnFVVnWe8YowSVhNOucbCIIakzihW6QTc7nPjCp-99qHcNF7ptpWdtr0vY08ZTQkWIqJojypnvXfalFvXbKTblRiVQ6Hl70Kj5eaQ3lcbXf8Yjg1GAO8BH6VupV25tr3r4o__Ck0OHrnS_-C_AUjiipY</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Pohl, Oliver</creator><creator>Perks, Deborah</creator><creator>Rhodes, Jon</creator><creator>Comotto, Laura</creator><creator>Baldrick, Paul</creator><creator>Chollet, André</creator><general>SAGE Publications</general><general>Springer International Publishing</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160401</creationdate><title>Effects of the Oral Oxytocin Receptor Antagonist Tocolytic OBE001 on Reproduction in Rats</title><author>Pohl, Oliver ; Perks, Deborah ; Rhodes, Jon ; Comotto, Laura ; Baldrick, Paul ; Chollet, André</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-2f304906a2d572aeae9f686907d4c87176bbd847b66526d2757e19f060ae451c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Embryology</topic><topic>Female</topic><topic>Male</topic><topic>Medicine & Public Health</topic><topic>Obstetrics/Perinatology/Midwifery</topic><topic>Original Article</topic><topic>Oximes - administration & dosage</topic><topic>Pregnancy</topic><topic>Pyrrolidines - administration & dosage</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Oxytocin - antagonists & inhibitors</topic><topic>Receptors, Oxytocin - physiology</topic><topic>Reproduction - drug effects</topic><topic>Reproduction - physiology</topic><topic>Reproductive Medicine</topic><topic>Tocolytic Agents - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pohl, Oliver</creatorcontrib><creatorcontrib>Perks, Deborah</creatorcontrib><creatorcontrib>Rhodes, Jon</creatorcontrib><creatorcontrib>Comotto, Laura</creatorcontrib><creatorcontrib>Baldrick, Paul</creatorcontrib><creatorcontrib>Chollet, André</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Reproductive sciences (Thousand Oaks, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pohl, Oliver</au><au>Perks, Deborah</au><au>Rhodes, Jon</au><au>Comotto, Laura</au><au>Baldrick, Paul</au><au>Chollet, André</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of the Oral Oxytocin Receptor Antagonist Tocolytic OBE001 on Reproduction in Rats</atitle><jtitle>Reproductive sciences (Thousand Oaks, Calif.)</jtitle><stitle>Reprod. Sci</stitle><addtitle>Reprod Sci</addtitle><date>2016-04-01</date><risdate>2016</risdate><volume>23</volume><issue>4</issue><spage>439</spage><epage>447</epage><pages>439-447</pages><issn>1933-7191</issn><eissn>1933-7205</eissn><abstract>Background:
OBE001 is a novel, orally active nonpeptide oxytocin receptor antagonist under development for the treatment of preterm labor and improvement in embryo implantation and pregnancy rate in assisted reproductive technology (ART). The reproductive safety of OBE001 was evaluated in customized fertility embryonic development (FER)/early embryonic development (EED) and fetal development (FD) and pre/postnatal development (PPN) studies mimicking clinical exposure scenarios.
Methods:
Oral OBE001 was evaluated at doses of 37.5, 75, and 125 mg/kg/d in female rats during a FER/EED study (from premating to implantation) and throughout FD during a FD/PPN study.
Results:
No OBE001 effects were observed during the FER/EED study. The FD/PPN study did not result in adverse OBE001 effects in females allowed to litter, their offspring, and second-generation fetuses. Females at 125 mg/kg/d who underwent cesarean section before term had slight reductions in body weights and food consumption, and associated fetuses had slightly delayed ossification of skull bones, which was not adverse in the absence of effects on live offspring.
Conclusion:
OBE001 at up to 125 mg/kg/d had no effects on EED and no adverse effects on FD and postnatal development of rats. These results constitute an important step toward the development of OBE001 in preterm labor and ART indications.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>26399985</pmid><doi>10.1177/1933719115607979</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals Embryology Female Male Medicine & Public Health Obstetrics/Perinatology/Midwifery Original Article Oximes - administration & dosage Pregnancy Pyrrolidines - administration & dosage Rats Rats, Sprague-Dawley Receptors, Oxytocin - antagonists & inhibitors Receptors, Oxytocin - physiology Reproduction - drug effects Reproduction - physiology Reproductive Medicine Tocolytic Agents - administration & dosage |
title | Effects of the Oral Oxytocin Receptor Antagonist Tocolytic OBE001 on Reproduction in Rats |
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