๐ฌIn plain words
What the trial is, and whether it could suit you
The objective of the study is to evaluate the efficacy and safety of T-bren in participants with HER2 expressing metastatic UC with progression on or after anti-PD-(L)1-based therapy.
Sign in to get the eligibility rules as simple questions to take to your doctor.
๐ Eligibility rules (as published)
Inclusion Criteria:
* Histologically or cytologically documented metastatic or surgically unresectable transitional cell carcinoma (TCC) of the urothelium involving the renal pelvis, ureter, bladder, or urethra. Minor histologic variants (ie, \<50% overall) are acceptable, provided that TCC is the dominant histology.
* Disease progression or recurrence during or following anti-PD-(L)1-based therapy.
* Fresh biopsy or archival tumor samples.
* Documented HER2 expression by central laboratory testing.
* Eligible to receive carboplatin or cisplatin in combination with gemcitabine.
* At least 1 measurable lesion based on RECIST v1.1.
* An Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 to 1.
* Adequate organ function.
* Adequate coagulation parameters.
Exclusion Criteria:
* Prior topoisomerase inhibitor-based ADC therapy.
* Primary tumors in the central nervous system (CNS), active or untreated CNS metastases, or carcinomatous meningitis.
* Bladder cancers with small cell histology.
* Other prior or concurrent malignancies except for certain localized cancers or low-grade prostate cancer (if approved by sponsor), or other malignancy treated with curative intent with a disease-free interval of at least 3 years.
* Prior history of clinically significant bleeding, or perforation of the gastrointestinal tract within 6 months of randomization.
* Active autoimmune diseases and inflammatory diseases.
* History of noninfectious interstitial lung disease (ILD)/pneumonitis that required treatment with steroids, have current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at Screening.
* Advanced/clinically significant lung disease (eg, poorly controlled chronic obstructive pulmonary disease or asthma, restrictive lung disease, or pulmonary hypertension) within 6 months prior to randomization.
* Known human immunodeficiency virus infection.
* Active hepatitis B virus (HBV) infection.
* Active hepatitis C virus (HCV) infection.
* Active or latent tuberculosis.
* Other protocol-specified inclusion/ exclusion criteria apply