{"id":121633,"date":"2026-08-28T01:03:14","date_gmt":"2026-08-28T01:03:14","guid":{"rendered":"https:\/\/www.europesays.com\/ch\/121633\/"},"modified":"2026-08-28T01:03:14","modified_gmt":"2026-08-28T01:03:14","slug":"chinese-biotech-files-worlds-first-approval-application-for-4-1bb-bispecific-antibody-abandoned-by-big-pharma-biggo-finance","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/ch\/121633\/","title":{"rendered":"Chinese Biotech Files World&#8217;s First Approval Application for 4-1BB Bispecific Antibody Abandoned by Big Pharma \u2014 BigGo Finance"},"content":{"rendered":"<p>Chinese biotech Leads Biolabs is challenging for the world&#8217;s first approval of a 4-1BB-targeting therapy, a target that global pharmaceutical companies had abandoned one after another due to toxicity concerns. The strategy involves using bispecific antibody technology to activate 4-1BB only in the vicinity of cancer cells, overcoming the limitations of previous therapies.<\/p>\n<p>According to biotech industry sources on the 28th, Leads Biolabs has filed for regulatory approval in China for Opartystomig, a bispecific antibody that simultaneously targets PD-L1 and 4-1BB. The drug has been designated for priority review and will undergo evaluation within 130 days. If approved, it would become the world&#8217;s first 4-1BB-targeting therapy.<\/p>\n<p>However, since key clinical efficacy data has not yet been disclosed, the extent to which the safety issues\u2014the biggest limitation of previous 4-1BB therapies\u2014have been improved will likely be the decisive factor in actual approval and market viability.<\/p>\n<p>4-1BB is an immune-activating receptor that promotes the activation and proliferation of immune T cells. If PD-1, a protein on the surface of cancer cells, acts as a brake that suppresses immune responses, then 4-1BB functions as an accelerator that enhances the attacking power of immune cells. Targeting PD-L1 and 4-1BB simultaneously helps the immune system recognize and attack cancer cells more effectively.<\/p>\n<p>While the anti-cancer efficacy is potent, systemic activation of 4-1BB has been a chronic problem, causing severe side effects including liver toxicity.<\/p>\n<p>Indeed, global big pharma companies repeatedly entered 4-1BB therapy development but failed to overcome the safety barrier. After U.S.-based Pfizer and Bristol Myers Squibb discontinued development, Switzerland&#8217;s Roche also announced in its first-quarter earnings this year that it was halting development of englumafusp alfa, a bispecific antibody targeting both CD19 and 4-1BB. Roche had already discontinued development of three 4-1BB candidates last year and is currently conducting a Phase 1 trial of Clesitomig, a 4-1BB trispecific antibody, in solid tumors.<\/p>\n<p>4-1BB-based bispecific antibodies work by simultaneously targeting a cancer cell surface protein and 4-1BB, boosting immune cell attack power only where cancer cells are present. This strategy aims to overcome the limitations of previous therapies, such as liver toxicity, by reducing systemic 4-1BB activation, and development competition has recently intensified. Approximately 80 4-1BB-related programs are currently known to be in development globally.<\/p>\n<p>South Korean companies are also entering the 4-1BB market with bispecific antibodies.<\/p>\n<p>ABL Bio is developing Javastomig (ABL111) and Rajistomig (ABL503), both based on its proprietary 4-1BB bispecific antibody platform Grabody-T. Javastomig simultaneously targets Claudin18.2, a cancer cell surface protein, and 4-1BB, and has demonstrated anti-cancer efficacy and tolerability in a Phase 1b trial. Rajistomig, like Leads Biolabs&#8217; candidate, simultaneously targets PD-L1 and 4-1BB and is currently preparing to enter Phase 1 trials. Both drugs are being co-developed by ABL Bio and U.S. biotech firm Novabridge Biosciences.<\/p>\n<p>Hanmi Pharmaceutical is also conducting a global Phase 1 trial of BH3120, a bispecific antibody targeting PD-L1 and 4-1BB. The trial is evaluating the drug as both monotherapy and in combination with Merck&#8217;s (MSD) Keytruda in patients with advanced or metastatic solid tumors in South Korea and the United States. BH3120 incorporates Hanmi Pharmaceutical&#8217;s Pentambody bispecific antibody platform, designed to activate immune cells while selectively attacking cancer cells.<\/p>\n<p>YH32367 (Nesprotamig), co-developed by Yuhan Corporation and ABL Bio, is another next-generation bispecific antibody candidate utilizing 4-1BB. It simultaneously targets HER2, which is expressed in major solid tumors, and 4-1BB. Phase 1\/2 trials are currently underway, with development targeting conditional approval in South Korea by 2028 and final approval by 2032.<\/p>\n<p>A South Korean industry official said, &#8220;4-1BB therapies were once considered a target that had hit a wall as big pharma companies abandoned development one after another. However, with the emergence of a new approach that activates 4-1BB only around tumors using bispecific antibodies, it is re-emerging as a key competitive field for next-generation immuno-oncology drugs.&#8221;<\/p>\n","protected":false},"excerpt":{"rendered":"Chinese biotech Leads Biolabs is challenging for the world&#8217;s first approval of a 4-1BB-targeting therapy, a target that&hellip;\n","protected":false},"author":2,"featured_media":121634,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":"","_share_on_mastodon":"0"},"categories":[124],"tags":[59356,59354,59359,58395,59357,59352,59353,41490,59358,134,59360,59355],"class_list":["post-121633","post","type-post","status-publish","format-standard","has-post-thumbnail","category-roche","tag-4-1bb","tag-abl-bio","tag-bh3120","tag-hanmi-pharmaceutical","tag-javastomig","tag-leads-biolabs","tag-opartystomig","tag-pd-l1","tag-rajistomig","tag-roche","tag-yh32367","tag-yuhan-corporation"],"share_on_mastodon":{"url":"https:\/\/pubeurope.com\/@ch\/117170445027240531","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts\/121633","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/comments?post=121633"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts\/121633\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/media\/121634"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/media?parent=121633"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/categories?post=121633"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/tags?post=121633"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}