Clinical development of ZW191 is planned to begin in the second half of 2024.
The IND application of ZW191, a TOPO1i FR⍺-targeted ADC, has been cleared by the FDA.1
“ZW191 is a differentiated product candidate in our pipeline that reflects the strength of our approach in developing best-in-class antibody-drug conjugates,” said Paul Moore, chief scientific officer of Zymeworks, in a press release. “Developed to target FR⍺, which is expressed in several types of difficult-to-treat cancers, ZW191 incorporates a novel antibody and drug-linker that provide a unique combination of antibody-linker stability and payload potency, together with strong bystander activity, which could result in improved efficacy and enable targeting lower levels of FR⍺ compared to previously developed drug candidates.”
Zymeworks seeks to begin clinical development of ZW191 later this year.
FR⍺ is expressed in several tumors, including in 75% of ovarian adenocarcinomas and 70% of NSCLC tumors. ZW191 uses a novel TOPO1i-based payload, ZD06519, to target FR⍺. The monoclonal antibody used is also able to target all levels of FR⍺ expression. According to preclinical models, ZW191 has demonstrated robust antitumor activity and tolerable safety.
In June 2024, the FDA cleared the IND application of ZW171, another Zymeworks agent. ZW171 is a bispecfic antibody targeting mesothelin-expressing cancers.2 Zymeworks’ preclinical pipeline also includes ZW251, a glypican-3 targeted TOPO1i ADC, and ZW220, a NaPi2b-targeted TOPO1i ADC.3
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