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Recruiting Phase 3

BL-M07D1 (Trastuzumab Brengitecan T-bren) vs Standard of Care Platinum-based Chemotherapy (PBC) for HER2-expressing Metastatic Urothelial Cancer After Progression on Anti-PD-(L)1-based Therapy

NCT07869836 · tracked via the Priya Life Science USA tracker
Phase
Phase 3
Started
2026-09
Last updated
2026-10-13

Condition(s) studied

Urothelial CancerMetastatic Urothelial CancerBladder CancerBladder Cancer (BC)Bladder (Urothelial, Transitional Cell) CancerBladder (Urothelial, Transitional Cell) Cancer Metastatic or UnresectableBladder CaBladder Cancer RecurrentBladder Cancer Stage IVUrothelial Carcinoma BladderUrothelial Carcinoma RecurrentUrothelial Carcinoma of the Urinary Bladder

Investigational drug(s) / intervention(s)

T-Bren, Dose level 1 →T-bren, Dose level 2 →Gemcitabine + Platinum Based Chemotherapy (Cisplatin or Carboplatin)All Gemcitabine trials (386) →All Carboplatin trials (593) →

T-Bren, Dose level 1: T-bren: Administered intravenously on day 1 of each 21-day cycle

T-bren, Dose level 2: TBren administered intravenously on day 1 of each 21-day cycle

Gemcitabine + Platinum Based Chemotherapy (Cisplatin or Carboplatin): Gemcitabine administered intravenously on Day 1 and Day 8 of each 21-day cycle and Cisplatin or Carboplatin administered intravenously on Day 1 of each 21-day cycle

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Progression-Free Survival (PFS) — Approximately 5 years
    Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) per RECIST v1.1 in the primary population

Trial sites (2)

FacilityCityRegionStatus
Central Georgia Cancer Center Macon Georgia Recruiting
Central Georgia Cancer Center Macon Georgia Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07869836 on ClinicalTrials.gov ↗ ← All trials in the USA