{"id":64767,"date":"2026-07-15T17:00:00","date_gmt":"2026-07-15T10:00:00","guid":{"rendered":"https:\/\/thaipropertynews.com\/feeds\/?p=64767"},"modified":"2026-07-15T17:00:00","modified_gmt":"2026-07-15T10:00:00","slug":"ascletis-selects-for-clinical-development-a-fixed-dose-combination-of-first-in-class-oral-small-molecule-gipr-agonist-asc48-and-oral-small-molecule-glp-1r-agonist-asc30","status":"publish","type":"post","link":"https:\/\/thaipropertynews.com\/feeds\/?p=64767","title":{"rendered":"Ascletis Selects for Clinical Development a Fixed-Dose Combination of First-in-Class Oral Small Molecule GIPR Agonist, ASC48, and Oral Small Molecule GLP-1R Agonist, ASC30"},"content":{"rendered":"<table border=\"0\" cellspacing=\"10\" cellpadding=\"5\" align=\"right\">\n<tbody>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mma.prnasia.com\/media2\/2935737\/Ascletis_Pharma_Logo.jpg?p=medium600\" border=\"0\" alt=\"\" title=\"logo\" hspace=\"0\" vspace=\"0\" width=\"118\" \/><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><i>&#8211; ASC48 is a potentially first-in-class oral small molecule GIPR agonist.<\/i><\/p>\n<p><i>&#8211; ASC48 demonstrated an EC<\/i><i><sub>50<\/sub><\/i><i> of 1 pM in the hGIPR cAMP activation assay, exhibiting greater potency than tirzepatide (EC<\/i><i><sub>50<\/sub><\/i><i> = 3 pM) and is a selective agonist for GIPR without activity for GLP-1R and GCGR.<\/i><\/p>\n<p><i>&#8211; ASC48 demonstrated excellent oral bioavailability and drug exposure as well as long half-life in rodents and non-human primates (NHPs), supporting once-daily oral dosing in humans.<\/i><\/p>\n<p><i>&#8211; Fixed dose combination of ASC30 and ASC48 (ASC30_48 FDC) is a potentially first-in-class oral one-pill, once-daily treatment for obesity, targeting both GLP-1R and GIPR.<\/i><\/p>\n<p><i>&#8211;<\/i> <i>ASC30_48 FDC demonstrated approximately 52% greater relative body weight reduction compared to ASC30 monotherapy in a head-to-head NHP study.<\/i><\/p>\n<p><i>&#8211; ASC30_48 FDC is a once-daily oral small molecule with the same mechanism of action as tirzepatide, the market leading GLP\/GIP once weekly subcutaneous peptide with over $30 billion in sales in 2025. <\/i><\/p>\n<p><i>&#8211; Submission of an Investigational New Drug Application (IND) to the U.S. Food and Drug Administration (FDA) for ASC30_48 FDC oral tablets is expected in the fourth quarter of 2026.<\/i><\/p>\n<p><span class=\"legendSpanClass\">HONG KONG<\/span>, <span class=\"legendSpanClass\">July 15, 2026<\/span> \/PRNewswire\/ &#8212; Ascletis Pharma Inc. (HKEX: 1672, &#8220;Ascletis&#8221;) announces that it has selected a fixed-dose combination of ASC48, a potentially first-in-class oral small molecule GIPR agonist, and ASC30, an oral small molecule GLP-1R agonist, for clinical development. ASC30 and ASC48 fixed-dose combination (ASC30_48 FDC) is a potentially first-in-class oral one-pill, once-daily therapy for obesity, targeting GLP-1R and GIPR.<\/p>\n<div class=\"PRN_ImbeddedAssetReference\">\n<\/div>\n<p>ASC48 was discovered in-house utilizing Ascletis&#8217; Artificial Intelligence-assisted Structure-Based Drug Discovery (AISBDD) technology. In a head-to-head study, ASC48 demonstrated an EC<sub>50 <\/sub>of 1 pM in the hGIPR cAMP activation assay, exhibiting greater potency than tirzepatide (EC<sub>50<\/sub> = 3 pM) and is a selective agonist for GIPR without activity for GLP-1R and GCGR. ASC48 demonstrated excellent oral bioavailability and drug exposure as well as long half-life in rodents and non-human primates (NHPs), supporting once-daily oral dosing in humans.<\/p>\n<p>ASC30_48 FDC demonstrated approximately 52% greater relative body weight reduction compared to ASC30 monotherapy in a head-to-head NHP study (Table 1).<\/p>\n<p>Table 1. Once-daily oral administration of ASC30_48 FDC for eight consecutive days produced 52% and 518% greater relative body weight reduction, respectively compared to ASC30 and ASC48 monotherapies<\/p>\n<div>\n<table border=\"0\" cellspacing=\"0\" cellpadding=\"1\" class=\"prnbcc\">\n<tbody>\n<tr>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Group<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Dosing<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Total body <br \/>weight change <br \/>from baseline<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Greater relative body\u00a0weight reduction versus <br \/>ASC30 monotherapy or <br \/>ASC48 monotherapy<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td class=\"prngen3\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">ASC30 (GLP-1R agonist)<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">2 mg\/kg<br \/>PO,\u00a0QD<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">-6.9\u00a0%<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">NA<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td class=\"prngen3\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">ASC48 (GIPR agonist)<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">5 mg\/kg<br \/>PO,\u00a0QD<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">-1.7\u00a0%<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">NA<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td class=\"prngen3\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">ASC30_48 FDC (GLP-<br \/>1R\/GIPR agonist)<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">2 mg\/kg ASC30 <br \/>and\u00a0<br \/>5 mg\/kg ASC48<\/span><\/p>\n<p class=\"prnml4\"><span class=\"prnews_span\">PO, QD<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">-10.5\u00a0%<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">52%<\/span><\/p>\n<p class=\"prnml4\"><span class=\"prnews_span\">(vs ASC30 monotherapy)<\/span><\/p>\n<p>518%<br \/>(vs ASC48\u00a0monotherapy)<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table><\/div>\n<p><i>Notes: <\/i><\/p>\n<p>PO: oral administration; QD: once daily.<\/p>\n<p>Submission of an Investigational New Drug Application (IND) to the U.S. Food and Drug Administration (FDA) for ASC30_48 FDC oral tablets is expected in the fourth quarter of 2026.<\/p>\n<p>&#8220;We look forward to initiating this trial to evaluate the fixed-dose combination of ASC48 and ASC30 with the aim of developing a first-in-class oral treatment regimen to potentially improve outcomes for people with obesity,&#8221; said Jinzi Jason Wu, Ph.D., Founder, Chairman and CEO of Ascletis. &#8220;We believe there is an unmet medical need for an oral drug that when given in combination with GLP-1R therapy can achieve the same weight loss and tolerability as tirzepatide weekly injections.&#8221;<\/p>\n<p><b>About Ascletis Pharma Inc.<\/b><\/p>\n<p>Ascletis Pharma Inc. is a fully integrated biotechnology company focused on the development and commercialization of potentially best-in-class and first-in-class therapeutics to treat metabolic diseases. Utilizing its proprietary Artificial Intelligence-assisted Structure-Based Drug Discovery (AISBDD) and Ultra-Long-Acting Platform (ULAP) technologies as well as Peptide Oral Transport ENhancement Technology (POTENT), Ascletis has developed multiple drug candidates in-house, including both small molecules and peptides, such as its lead program, ASC30, a small molecule GLP-1R agonist designed to be administered once daily orally and once monthly to once quarterly subcutaneously as a treatment therapy and a maintenance therapy for chronic weight management; ASC36, an amylin receptor peptide agonist, ASC35, a once-monthly subcutaneously administered GLP-1R\/GIPR dual peptide agonist and ASC37, a GLP-1R\/GIPR\/GCGR triple peptide agonist, ASC39, an eloralintide-like potent and amylin-selective oral small molecule amylin receptor agonist, ASC30_39 FDC, a fixed-dose combination (FDC) of ASC30 (GLP-1 RA) and ASC39 (amylin RA), ASC30_48 FDC, a fixed-dose combination (FDC) of ASC30 (GLP-1 RA) and ASC48 (GIP RA),for chronic weight management. Ascletis is listed on the Hong Kong Stock Exchange (1672.HK).<\/p>\n<p>For more information, please visit <a href=\"https:\/\/www.ascletis.com\/\" target=\"_blank\" rel=\"nofollow\">www.ascletis.com<\/a>.\u00a0<\/p>\n<p>Contact\uff1a<\/p>\n<p>Peter Vozzo<br \/>ICR Healthcare<br \/>443-231-0505 (U.S.)<br \/><a href=\"mailto:Peter.vozzo@icrhealthcare.com\" target=\"_blank\" rel=\"nofollow\">Peter.vozzo@icrhealthcare.com<\/a>\u00a0<\/p>\n<p>Ascletis Pharma Inc. PR and IR Teams<br \/>+86-181-0650-9129 (China)<br \/><a href=\"mailto:pr@ascletis.com\" target=\"_blank\" rel=\"nofollow\">pr@ascletis.com<\/a> <br \/><a href=\"mailto:ir@ascletis.com\" target=\"_blank\" rel=\"nofollow\">ir@ascletis.com<\/a>\u00a0<\/p>","protected":false},"excerpt":{"rendered":"<p><!-- wp:html --><\/p>\n<table border=\"0\" cellspacing=\"10\" cellpadding=\"5\" align=\"right\">\n<tbody>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mma.prnasia.com\/media2\/2935737\/Ascletis_Pharma_Logo.jpg?p=medium600\" border=\"0\" alt=\"\" title=\"logo\" hspace=\"0\" vspace=\"0\" width=\"118\" \/><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><i>&#8211; ASC48 is a potentially first-in-class oral small molecule GIPR agonist.<\/i><\/p>\n<p><i>&#8211; ASC48 demonstrated an EC<\/i><i><sub>50<\/sub><\/i><i> of 1 pM in the hGIPR cAMP activation assay, exhibiting greater potency than tirzepatide (EC<\/i><i><sub>50<\/sub><\/i><i> = 3 pM) and is a selective agonist for GIPR without activity for GLP-1R and GCGR.<\/i><\/p>\n<p><i>&#8211; ASC48 demonstrated excellent oral bioavailability and drug exposure as well as long half-life in rodents and non-human primates (NHPs), supporting once-daily oral dosing in humans.<\/i><\/p>\n<p><i>&#8211; Fixed dose combination of ASC30 and ASC48 (ASC30_48 FDC) is a potentially first-in-class oral one-pill, once-daily treatment for obesity, targeting both GLP-1R and GIPR.<\/i><\/p>\n<p><i>&#8211;<\/i> <i>ASC30_48 FDC demonstrated approximately 52% greater relative body weight reduction compared to ASC30 monotherapy in a head-to-head NHP study.<\/i><\/p>\n<p><i>&#8211; ASC30_48 FDC is a once-daily oral small molecule with the same mechanism of action as tirzepatide, the market leading GLP\/GIP once weekly subcutaneous peptide with over $30 billion in sales in 2025. <\/i><\/p>\n<p><i>&#8211; Submission of an Investigational New Drug Application (IND) to the U.S. Food and Drug Administration (FDA) for ASC30_48 FDC oral tablets is expected in the fourth quarter of 2026.<\/i><\/p>\n<p><span class=\"legendSpanClass\">HONG KONG<\/span>, <span class=\"legendSpanClass\">July 15, 2026<\/span> \/PRNewswire\/ &#8212; Ascletis Pharma Inc. (HKEX: 1672, &#8220;Ascletis&#8221;) announces that it has selected a fixed-dose combination of ASC48, a potentially first-in-class oral small molecule GIPR agonist, and ASC30, an oral small molecule GLP-1R agonist, for clinical development. ASC30 and ASC48 fixed-dose combination (ASC30_48 FDC) is a potentially first-in-class oral one-pill, once-daily therapy for obesity, targeting GLP-1R and GIPR.<\/p>\n<div class=\"PRN_ImbeddedAssetReference\">\n<\/div>\n<p>ASC48 was discovered in-house utilizing Ascletis&#8217; Artificial Intelligence-assisted Structure-Based Drug Discovery (AISBDD) technology. In a head-to-head study, ASC48 demonstrated an EC<sub>50 <\/sub>of 1 pM in the hGIPR cAMP activation assay, exhibiting greater potency than tirzepatide (EC<sub>50<\/sub> = 3 pM) and is a selective agonist for GIPR without activity for GLP-1R and GCGR. ASC48 demonstrated excellent oral bioavailability and drug exposure as well as long half-life in rodents and non-human primates (NHPs), supporting once-daily oral dosing in humans.<\/p>\n<p>ASC30_48 FDC demonstrated approximately 52% greater relative body weight reduction compared to ASC30 monotherapy in a head-to-head NHP study (Table 1).<\/p>\n<p>Table 1. Once-daily oral administration of ASC30_48 FDC for eight consecutive days produced 52% and 518% greater relative body weight reduction, respectively compared to ASC30 and ASC48 monotherapies<\/p>\n<div>\n<table border=\"0\" cellspacing=\"0\" cellpadding=\"1\" class=\"prnbcc\">\n<tbody>\n<tr>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Group<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Dosing<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Total body <br \/>weight change <br \/>from baseline<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">Greater relative body\u00a0weight reduction versus <br \/>ASC30 monotherapy or <br \/>ASC48 monotherapy<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td class=\"prngen3\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">ASC30 (GLP-1R agonist)<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">2 mg\/kg<br \/>PO,\u00a0QD<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">-6.9\u00a0%<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">NA<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td class=\"prngen3\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">ASC48 (GIPR agonist)<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">5 mg\/kg<br \/>PO,\u00a0QD<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">-1.7\u00a0%<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">NA<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td class=\"prngen3\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">ASC30_48 FDC (GLP-<br \/>1R\/GIPR agonist)<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">2 mg\/kg ASC30 <br \/>and\u00a0<br \/>5 mg\/kg ASC48<\/span><\/p>\n<p class=\"prnml4\"><span class=\"prnews_span\">PO, QD<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">-10.5\u00a0%<\/span><\/p>\n<\/td>\n<td class=\"prngen2\" colspan=\"1\" rowspan=\"1\" nowrap>\n<p class=\"prnml4\"><span class=\"prnews_span\">52%<\/span><\/p>\n<p class=\"prnml4\"><span class=\"prnews_span\">(vs ASC30 monotherapy)<\/span><\/p>\n<p>518%<br \/>(vs ASC48\u00a0monotherapy)<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<p><i>Notes: <\/i><\/p>\n<p>PO: oral administration; QD: once daily.<\/p>\n<p>Submission of an Investigational New Drug Application (IND) to the U.S. Food and Drug Administration (FDA) for ASC30_48 FDC oral tablets is expected in the fourth quarter of 2026.<\/p>\n<p>&#8220;We look forward to initiating this trial to evaluate the fixed-dose combination of ASC48 and ASC30 with the aim of developing a first-in-class oral treatment regimen to potentially improve outcomes for people with obesity,&#8221; said Jinzi Jason Wu, Ph.D., Founder, Chairman and CEO of Ascletis. &#8220;We believe there is an unmet medical need for an oral drug that when given in combination with GLP-1R therapy can achieve the same weight loss and tolerability as tirzepatide weekly injections.&#8221;<\/p>\n<p><b>About Ascletis Pharma Inc.<\/b><\/p>\n<p>Ascletis Pharma Inc. is a fully integrated biotechnology company focused on the development and commercialization of potentially best-in-class and first-in-class therapeutics to treat metabolic diseases. Utilizing its proprietary Artificial Intelligence-assisted Structure-Based Drug Discovery (AISBDD) and Ultra-Long-Acting Platform (ULAP) technologies as well as Peptide Oral Transport ENhancement Technology (POTENT), Ascletis has developed multiple drug candidates in-house, including both small molecules and peptides, such as its lead program, ASC30, a small molecule GLP-1R agonist designed to be administered once daily orally and once monthly to once quarterly subcutaneously as a treatment therapy and a maintenance therapy for chronic weight management; ASC36, an amylin receptor peptide agonist, ASC35, a once-monthly subcutaneously administered GLP-1R\/GIPR dual peptide agonist and ASC37, a GLP-1R\/GIPR\/GCGR triple peptide agonist, ASC39, an eloralintide-like potent and amylin-selective oral small molecule amylin receptor agonist, ASC30_39 FDC, a fixed-dose combination (FDC) of ASC30 (GLP-1 RA) and ASC39 (amylin RA), ASC30_48 FDC, a fixed-dose combination (FDC) of ASC30 (GLP-1 RA) and ASC48 (GIP RA),for chronic weight management. Ascletis is listed on the Hong Kong Stock Exchange (1672.HK).<\/p>\n<p>For more information, please visit <a href=\"https:\/\/www.ascletis.com\/\" target=\"_blank\" rel=\"nofollow\">www.ascletis.com<\/a>.\u00a0<\/p>\n<p>Contact\uff1a<\/p>\n<p>Peter Vozzo<br \/>ICR Healthcare<br \/>443-231-0505 (U.S.)<br \/><a href=\"mailto:Peter.vozzo@icrhealthcare.com\" target=\"_blank\" rel=\"nofollow\">Peter.vozzo@icrhealthcare.com<\/a>\u00a0<\/p>\n<p>Ascletis Pharma Inc. PR and IR Teams<br \/>+86-181-0650-9129 (China)<br \/><a href=\"mailto:pr@ascletis.com\" target=\"_blank\" rel=\"nofollow\">pr@ascletis.com<\/a> <br \/><a href=\"mailto:ir@ascletis.com\" target=\"_blank\" rel=\"nofollow\">ir@ascletis.com<\/a>\u00a0<\/p>\n<p><!-- \/wp:html --><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"rop_custom_images_group":[],"rop_custom_messages_group":[],"rop_publish_now":"initial","rop_publish_now_accounts":[],"rop_publish_now_history":[],"rop_publish_now_status":"pending","footnotes":""},"categories":[5,7],"tags":[],"class_list":["post-64767","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-cision-pr-newswire","category-cision-pr-newswire-en"],"_links":{"self":[{"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=\/wp\/v2\/posts\/64767","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=64767"}],"version-history":[{"count":0,"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=\/wp\/v2\/posts\/64767\/revisions"}],"wp:attachment":[{"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=64767"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=64767"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/thaipropertynews.com\/feeds\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=64767"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}