Loading…
LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept
With an increasing prevalence of obesity, there is a need for new therapies to improve body weight management and metabolic health. Multireceptor agonists in development may provide approaches to fulfill this unmet medical need. LY3437943 is a novel triple agonist peptide at the glucagon receptor (G...
Saved in:
Published in: | Cell metabolism 2022-09, Vol.34 (9), p.1234-1247.e9 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c443t-ca529acf546eee993aee7c4b782498152da82811299bea7c5e51eee021b88aa23 |
---|---|
cites | cdi_FETCH-LOGICAL-c443t-ca529acf546eee993aee7c4b782498152da82811299bea7c5e51eee021b88aa23 |
container_end_page | 1247.e9 |
container_issue | 9 |
container_start_page | 1234 |
container_title | Cell metabolism |
container_volume | 34 |
creator | Coskun, Tamer Urva, Shweta Roell, William C. Qu, Hongchang Loghin, Corina Moyers, Julie S. O’Farrell, Libbey S. Briere, Daniel A. Sloop, Kyle W. Thomas, Melissa K. Pirro, Valentina Wainscott, David B. Willard, Francis S. Abernathy, Matthew Morford, LaRonda Du, Yu Benson, Charles Gimeno, Ruth E. Haupt, Axel Milicevic, Zvonko |
description | With an increasing prevalence of obesity, there is a need for new therapies to improve body weight management and metabolic health. Multireceptor agonists in development may provide approaches to fulfill this unmet medical need. LY3437943 is a novel triple agonist peptide at the glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). In vitro, LY3437943 shows balanced GCGR and GLP-1R activity but more GIPR activity. In obese mice, administration of LY3437943 decreased body weight and improved glycemic control. Body weight loss was augmented by the addition of GCGR-mediated increases in energy expenditure to GIPR- and GLP-1R-driven calorie intake reduction. In a phase 1 single ascending dose study, LY3437943 showed a safety and tolerability profile similar to other incretins. Its pharmacokinetic profile supported once-weekly dosing, and a reduction in body weight persisted up to day 43 after a single dose. These findings warrant further clinical assessment of LY3437943.
[Display omitted]
•LY3437943 has triple agonist activity at the glucagon, GIP, and GLP-1 receptors•LY3437943 caused greater body weight loss in obese mice than tirzepatide•LY3437943 increased energy expenditure through glucagon receptor activation•Safety and tolerability of LY3437943 were similar to other incretin-based drugs
Coskun et al. demonstrate that LY3437943, a triple glucagon, GIP, and GLP-1 receptor agonist for the treatment of obesity and type 2 diabetes, can reduce body weight through increased energy expenditure and reduced calorie intake in obese mice. Its safety and tolerability in healthy participants were similar to other incretin-based therapies. |
doi_str_mv | 10.1016/j.cmet.2022.07.013 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2704871941</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1550413122003126</els_id><sourcerecordid>2704871941</sourcerecordid><originalsourceid>FETCH-LOGICAL-c443t-ca529acf546eee993aee7c4b782498152da82811299bea7c5e51eee021b88aa23</originalsourceid><addsrcrecordid>eNp9UU1vEzEQtRBIlMAf4DRHDt2tvzZeIy6oakOlSPQAB06W450NjrzrYDtF-SH8X7ykZ6SRZqR5b2bePELeM9oyytY3h9ZNWFpOOW-paikTL8gV04I3SnL6stZdRxvJBHtN3uR8oFSshRZX5M_2h5BCaSmuwcIcnzBASf4YEPbh5Ow-zteweXis3XmAzfaxYZDQ4bHEBEvX5wJjrffh7HDyDlycS4rhH_43-v3PAiHm_BHuU5xg8NnVJekMJYILfvbOBjimGEeoUcnL7Lfk1WhDxnfPeUW-3999u_3SbL9uHm4_bxsnpSiNsx3X1o2dXCOi1sIiKid3qudS96zjg-15zxjXeodWuQ47VoGUs13fW8vFiny4zK0H_DphLmaq92EIdsZ4yoYrKnvFdH3civAL1KWqJuFojslPNp0No2bxwBzM4oFZPDBUmepBJX26kLCKePKYTHYeq8TB1ycWM0T_P_pfP_mP9w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2704871941</pqid></control><display><type>article</type><title>LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept</title><source>BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS</source><creator>Coskun, Tamer ; Urva, Shweta ; Roell, William C. ; Qu, Hongchang ; Loghin, Corina ; Moyers, Julie S. ; O’Farrell, Libbey S. ; Briere, Daniel A. ; Sloop, Kyle W. ; Thomas, Melissa K. ; Pirro, Valentina ; Wainscott, David B. ; Willard, Francis S. ; Abernathy, Matthew ; Morford, LaRonda ; Du, Yu ; Benson, Charles ; Gimeno, Ruth E. ; Haupt, Axel ; Milicevic, Zvonko</creator><creatorcontrib>Coskun, Tamer ; Urva, Shweta ; Roell, William C. ; Qu, Hongchang ; Loghin, Corina ; Moyers, Julie S. ; O’Farrell, Libbey S. ; Briere, Daniel A. ; Sloop, Kyle W. ; Thomas, Melissa K. ; Pirro, Valentina ; Wainscott, David B. ; Willard, Francis S. ; Abernathy, Matthew ; Morford, LaRonda ; Du, Yu ; Benson, Charles ; Gimeno, Ruth E. ; Haupt, Axel ; Milicevic, Zvonko</creatorcontrib><description>With an increasing prevalence of obesity, there is a need for new therapies to improve body weight management and metabolic health. Multireceptor agonists in development may provide approaches to fulfill this unmet medical need. LY3437943 is a novel triple agonist peptide at the glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). In vitro, LY3437943 shows balanced GCGR and GLP-1R activity but more GIPR activity. In obese mice, administration of LY3437943 decreased body weight and improved glycemic control. Body weight loss was augmented by the addition of GCGR-mediated increases in energy expenditure to GIPR- and GLP-1R-driven calorie intake reduction. In a phase 1 single ascending dose study, LY3437943 showed a safety and tolerability profile similar to other incretins. Its pharmacokinetic profile supported once-weekly dosing, and a reduction in body weight persisted up to day 43 after a single dose. These findings warrant further clinical assessment of LY3437943.
[Display omitted]
•LY3437943 has triple agonist activity at the glucagon, GIP, and GLP-1 receptors•LY3437943 caused greater body weight loss in obese mice than tirzepatide•LY3437943 increased energy expenditure through glucagon receptor activation•Safety and tolerability of LY3437943 were similar to other incretin-based drugs
Coskun et al. demonstrate that LY3437943, a triple glucagon, GIP, and GLP-1 receptor agonist for the treatment of obesity and type 2 diabetes, can reduce body weight through increased energy expenditure and reduced calorie intake in obese mice. Its safety and tolerability in healthy participants were similar to other incretin-based therapies.</description><identifier>ISSN: 1550-4131</identifier><identifier>EISSN: 1932-7420</identifier><identifier>DOI: 10.1016/j.cmet.2022.07.013</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>energy expenditure ; GIP ; GLP-1 ; glucagon ; glucose control ; metabolomics ; obesity ; triple agonist</subject><ispartof>Cell metabolism, 2022-09, Vol.34 (9), p.1234-1247.e9</ispartof><rights>2022 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-ca529acf546eee993aee7c4b782498152da82811299bea7c5e51eee021b88aa23</citedby><cites>FETCH-LOGICAL-c443t-ca529acf546eee993aee7c4b782498152da82811299bea7c5e51eee021b88aa23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Coskun, Tamer</creatorcontrib><creatorcontrib>Urva, Shweta</creatorcontrib><creatorcontrib>Roell, William C.</creatorcontrib><creatorcontrib>Qu, Hongchang</creatorcontrib><creatorcontrib>Loghin, Corina</creatorcontrib><creatorcontrib>Moyers, Julie S.</creatorcontrib><creatorcontrib>O’Farrell, Libbey S.</creatorcontrib><creatorcontrib>Briere, Daniel A.</creatorcontrib><creatorcontrib>Sloop, Kyle W.</creatorcontrib><creatorcontrib>Thomas, Melissa K.</creatorcontrib><creatorcontrib>Pirro, Valentina</creatorcontrib><creatorcontrib>Wainscott, David B.</creatorcontrib><creatorcontrib>Willard, Francis S.</creatorcontrib><creatorcontrib>Abernathy, Matthew</creatorcontrib><creatorcontrib>Morford, LaRonda</creatorcontrib><creatorcontrib>Du, Yu</creatorcontrib><creatorcontrib>Benson, Charles</creatorcontrib><creatorcontrib>Gimeno, Ruth E.</creatorcontrib><creatorcontrib>Haupt, Axel</creatorcontrib><creatorcontrib>Milicevic, Zvonko</creatorcontrib><title>LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept</title><title>Cell metabolism</title><description>With an increasing prevalence of obesity, there is a need for new therapies to improve body weight management and metabolic health. Multireceptor agonists in development may provide approaches to fulfill this unmet medical need. LY3437943 is a novel triple agonist peptide at the glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). In vitro, LY3437943 shows balanced GCGR and GLP-1R activity but more GIPR activity. In obese mice, administration of LY3437943 decreased body weight and improved glycemic control. Body weight loss was augmented by the addition of GCGR-mediated increases in energy expenditure to GIPR- and GLP-1R-driven calorie intake reduction. In a phase 1 single ascending dose study, LY3437943 showed a safety and tolerability profile similar to other incretins. Its pharmacokinetic profile supported once-weekly dosing, and a reduction in body weight persisted up to day 43 after a single dose. These findings warrant further clinical assessment of LY3437943.
[Display omitted]
•LY3437943 has triple agonist activity at the glucagon, GIP, and GLP-1 receptors•LY3437943 caused greater body weight loss in obese mice than tirzepatide•LY3437943 increased energy expenditure through glucagon receptor activation•Safety and tolerability of LY3437943 were similar to other incretin-based drugs
Coskun et al. demonstrate that LY3437943, a triple glucagon, GIP, and GLP-1 receptor agonist for the treatment of obesity and type 2 diabetes, can reduce body weight through increased energy expenditure and reduced calorie intake in obese mice. Its safety and tolerability in healthy participants were similar to other incretin-based therapies.</description><subject>energy expenditure</subject><subject>GIP</subject><subject>GLP-1</subject><subject>glucagon</subject><subject>glucose control</subject><subject>metabolomics</subject><subject>obesity</subject><subject>triple agonist</subject><issn>1550-4131</issn><issn>1932-7420</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9UU1vEzEQtRBIlMAf4DRHDt2tvzZeIy6oakOlSPQAB06W450NjrzrYDtF-SH8X7ykZ6SRZqR5b2bePELeM9oyytY3h9ZNWFpOOW-paikTL8gV04I3SnL6stZdRxvJBHtN3uR8oFSshRZX5M_2h5BCaSmuwcIcnzBASf4YEPbh5Ow-zteweXis3XmAzfaxYZDQ4bHEBEvX5wJjrffh7HDyDlycS4rhH_43-v3PAiHm_BHuU5xg8NnVJekMJYILfvbOBjimGEeoUcnL7Lfk1WhDxnfPeUW-3999u_3SbL9uHm4_bxsnpSiNsx3X1o2dXCOi1sIiKid3qudS96zjg-15zxjXeodWuQ47VoGUs13fW8vFiny4zK0H_DphLmaq92EIdsZ4yoYrKnvFdH3civAL1KWqJuFojslPNp0No2bxwBzM4oFZPDBUmepBJX26kLCKePKYTHYeq8TB1ycWM0T_P_pfP_mP9w</recordid><startdate>20220906</startdate><enddate>20220906</enddate><creator>Coskun, Tamer</creator><creator>Urva, Shweta</creator><creator>Roell, William C.</creator><creator>Qu, Hongchang</creator><creator>Loghin, Corina</creator><creator>Moyers, Julie S.</creator><creator>O’Farrell, Libbey S.</creator><creator>Briere, Daniel A.</creator><creator>Sloop, Kyle W.</creator><creator>Thomas, Melissa K.</creator><creator>Pirro, Valentina</creator><creator>Wainscott, David B.</creator><creator>Willard, Francis S.</creator><creator>Abernathy, Matthew</creator><creator>Morford, LaRonda</creator><creator>Du, Yu</creator><creator>Benson, Charles</creator><creator>Gimeno, Ruth E.</creator><creator>Haupt, Axel</creator><creator>Milicevic, Zvonko</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20220906</creationdate><title>LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept</title><author>Coskun, Tamer ; Urva, Shweta ; Roell, William C. ; Qu, Hongchang ; Loghin, Corina ; Moyers, Julie S. ; O’Farrell, Libbey S. ; Briere, Daniel A. ; Sloop, Kyle W. ; Thomas, Melissa K. ; Pirro, Valentina ; Wainscott, David B. ; Willard, Francis S. ; Abernathy, Matthew ; Morford, LaRonda ; Du, Yu ; Benson, Charles ; Gimeno, Ruth E. ; Haupt, Axel ; Milicevic, Zvonko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-ca529acf546eee993aee7c4b782498152da82811299bea7c5e51eee021b88aa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>energy expenditure</topic><topic>GIP</topic><topic>GLP-1</topic><topic>glucagon</topic><topic>glucose control</topic><topic>metabolomics</topic><topic>obesity</topic><topic>triple agonist</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Coskun, Tamer</creatorcontrib><creatorcontrib>Urva, Shweta</creatorcontrib><creatorcontrib>Roell, William C.</creatorcontrib><creatorcontrib>Qu, Hongchang</creatorcontrib><creatorcontrib>Loghin, Corina</creatorcontrib><creatorcontrib>Moyers, Julie S.</creatorcontrib><creatorcontrib>O’Farrell, Libbey S.</creatorcontrib><creatorcontrib>Briere, Daniel A.</creatorcontrib><creatorcontrib>Sloop, Kyle W.</creatorcontrib><creatorcontrib>Thomas, Melissa K.</creatorcontrib><creatorcontrib>Pirro, Valentina</creatorcontrib><creatorcontrib>Wainscott, David B.</creatorcontrib><creatorcontrib>Willard, Francis S.</creatorcontrib><creatorcontrib>Abernathy, Matthew</creatorcontrib><creatorcontrib>Morford, LaRonda</creatorcontrib><creatorcontrib>Du, Yu</creatorcontrib><creatorcontrib>Benson, Charles</creatorcontrib><creatorcontrib>Gimeno, Ruth E.</creatorcontrib><creatorcontrib>Haupt, Axel</creatorcontrib><creatorcontrib>Milicevic, Zvonko</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cell metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coskun, Tamer</au><au>Urva, Shweta</au><au>Roell, William C.</au><au>Qu, Hongchang</au><au>Loghin, Corina</au><au>Moyers, Julie S.</au><au>O’Farrell, Libbey S.</au><au>Briere, Daniel A.</au><au>Sloop, Kyle W.</au><au>Thomas, Melissa K.</au><au>Pirro, Valentina</au><au>Wainscott, David B.</au><au>Willard, Francis S.</au><au>Abernathy, Matthew</au><au>Morford, LaRonda</au><au>Du, Yu</au><au>Benson, Charles</au><au>Gimeno, Ruth E.</au><au>Haupt, Axel</au><au>Milicevic, Zvonko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept</atitle><jtitle>Cell metabolism</jtitle><date>2022-09-06</date><risdate>2022</risdate><volume>34</volume><issue>9</issue><spage>1234</spage><epage>1247.e9</epage><pages>1234-1247.e9</pages><issn>1550-4131</issn><eissn>1932-7420</eissn><abstract>With an increasing prevalence of obesity, there is a need for new therapies to improve body weight management and metabolic health. Multireceptor agonists in development may provide approaches to fulfill this unmet medical need. LY3437943 is a novel triple agonist peptide at the glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). In vitro, LY3437943 shows balanced GCGR and GLP-1R activity but more GIPR activity. In obese mice, administration of LY3437943 decreased body weight and improved glycemic control. Body weight loss was augmented by the addition of GCGR-mediated increases in energy expenditure to GIPR- and GLP-1R-driven calorie intake reduction. In a phase 1 single ascending dose study, LY3437943 showed a safety and tolerability profile similar to other incretins. Its pharmacokinetic profile supported once-weekly dosing, and a reduction in body weight persisted up to day 43 after a single dose. These findings warrant further clinical assessment of LY3437943.
[Display omitted]
•LY3437943 has triple agonist activity at the glucagon, GIP, and GLP-1 receptors•LY3437943 caused greater body weight loss in obese mice than tirzepatide•LY3437943 increased energy expenditure through glucagon receptor activation•Safety and tolerability of LY3437943 were similar to other incretin-based drugs
Coskun et al. demonstrate that LY3437943, a triple glucagon, GIP, and GLP-1 receptor agonist for the treatment of obesity and type 2 diabetes, can reduce body weight through increased energy expenditure and reduced calorie intake in obese mice. Its safety and tolerability in healthy participants were similar to other incretin-based therapies.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.cmet.2022.07.013</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1550-4131 |
ispartof | Cell metabolism, 2022-09, Vol.34 (9), p.1234-1247.e9 |
issn | 1550-4131 1932-7420 |
language | eng |
recordid | cdi_proquest_miscellaneous_2704871941 |
source | BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS |
subjects | energy expenditure GIP GLP-1 glucagon glucose control metabolomics obesity triple agonist |
title | LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T23%3A49%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=LY3437943,%20a%20novel%20triple%20glucagon,%20GIP,%20and%20GLP-1%20receptor%20agonist%20for%20glycemic%20control%20and%20weight%20loss:%20From%20discovery%20to%20clinical%20proof%20of%20concept&rft.jtitle=Cell%20metabolism&rft.au=Coskun,%20Tamer&rft.date=2022-09-06&rft.volume=34&rft.issue=9&rft.spage=1234&rft.epage=1247.e9&rft.pages=1234-1247.e9&rft.issn=1550-4131&rft.eissn=1932-7420&rft_id=info:doi/10.1016/j.cmet.2022.07.013&rft_dat=%3Cproquest_cross%3E2704871941%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c443t-ca529acf546eee993aee7c4b782498152da82811299bea7c5e51eee021b88aa23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2704871941&rft_id=info:pmid/&rfr_iscdi=true |