ATTN: We are committed to keeping our patients informed regarding the recent cybersecurity incident involving McKesson. At this time, we are continuing to monitor the situation closely and are working to obtain the most current information available. We will provide updates as we receive additional information from McKesson and learn more about any potential impact. Thank you for your patience and trust as we navigate this situation together. CLICK HERE for more information.

Clinical Research & Trials

USO 25175

C6461006: AN INTERVENTIONAL PHASE 1b/2, OPEN-LABEL STUDY TO INVESTIGATE THE SAFETY, ANTITUMOR ACTIVITY, AND PHARMACOKINETICS OF PF08634404 MONOTHERAPY OR IN COMBINATION WITH ENFORTUMAB VEDOTIN IN ADULT PARTICIPANTS WITH LOCALLY ADVANCED OR METASTATIC UROTHELIAL CANCER

 

Disease Types: Genitourinary Cancer Research

Eligibility Requirements:

• Histologically documented unresectable locally
advanced or metastatic urothelial cancer
• Cohort A: Previously treated (≤3 LOT) disease
• Prior platinum-containing therapy is allowed
• Cohort B: Previously untreated disease
• Subjects must have sufficient tumor tissue available
• Measurable disease based on RECIST 1.1
• Subjects with known active CNS lesions, including
leptomeningeal metastasis, brainstem, meningeal, or
spinal cord metastases or compression are excluded

For more details on this trial CLICK HERE .

Available at: