Targeted therapies for urothelial carcinoma: From FGFR inhibitors to next‑generation antibody-drug conjugates (Review). [PDF]
Du J, Shen H, Zeng T, Liu W, Xie Y.
europepmc +1 more source
Correction: Petsas et al. Protein-Ligand Interactions in Cardiometabolic Drug Targets: Focus on Weight Loss and Cardioprotection. <i>Molecules</i> 2025, <i>30</i>, 4240. [PDF]
Petsas E +5 more
europepmc +1 more source
Design characteristics of mass balance studies conducted for protein kinase inhibitors. [PDF]
Riechelman B +5 more
europepmc +1 more source
Phase Ib Trial of Fulvestrant, Palbociclib, and Erdafitinib, a pan-FGFR Tyrosine Kinase Inhibitor, in HR+/HER2- Metastatic Breast Cancer. [PDF]
Gonzalez-Ericsson PI +14 more
europepmc +1 more source
Bladder-Preserving Platforms for BCG-Unresponsive Non-Muscle-Invasive Bladder Cancer. [PDF]
Zhang K, Ren Y.
europepmc +1 more source
<i>FGFR3</i> Gene Alterations and Protein Expression in Paired TURBT and Radical Cystectomy Archival Specimens of Muscle-Invasive Bladder Cancer. [PDF]
Miyake M +14 more
europepmc +1 more source
Erdafitinib in Locally Advanced or Metastatic Urothelial Carcinoma
Alterations in the gene encoding fibroblast growth factor receptor (FGFR) are common in urothelial carcinoma and may be associated with lower sensitivity to immune interventions. Erdafitinib, a tyrosine kinase inhibitor of FGFR1-4, has shown antitumor activity in preclinical models and in a phase 1 study involving patients with FGFR alterations.In this
Jesus Garcia-donas +2 more
exaly +6 more sources
Erdafitinib in BCG-Treated High-Risk Non-Muscle-Invasive Bladder Cancer [PDF]
Background: Treatment options are limited for patients with high-risk non-muscle-invasive bladder cancer (NMIBC) with disease recurrence after bacillus Calmette–Guérin (BCG) treatment and who are ineligible for/refuse radical cystectomy. FGFR alterations
Bladou Franck, Rosa Tambaro, S Triantos
exaly +5 more sources

