Natera Seeks PMDA Approval for Signatera CDx in MIBC

Shots: Natera has submitted an application to Japan’s PMDA seeking approval of Signatera as a companion diagnostic (CDx) for muscle-invasive bladder cancer (MIBC) The submission expands the company’s presence in Japan, where Signatera became the country’s first PMDA-approved molecular residual disease (MRD) test for colorectal cancer in Jun 2026 Application is supported by data from the P-III (IMvigor011) trial & builds on milestones, incl. the US FDA approval of Signatera CDx as a companion diagnostic for adj. Tecentriq & a Category 1 NCCN recommendation for Signatera MRD-guided adj. Tecentriq in bladder cancer Ref: Businesswire  |  Image: Natera  |  Press Release R PharmaShots, your go-to media platform for customized news ranging across multiple indications. For more information, connect with us at connect@pharmashots.com The post Natera Seeks PMDA Approval for Signatera CDx in MIBC appeared first on PharmaShots.