Bladder Cancer Clinical Trial

A Study Of Avelumab In Patients With Locally Advanced Or Metastatic Urothelial Cancer (JAVELIN Bladder 100)

Summary

The main purpose of this study is to compare maintenance treatment with avelumab plus best supportive care (BSC) with BSC alone, to determine if avelumab has an effect on survival in patients with locally advanced or metastatic urothelial cancer that did not worsen during or following completion of first-line chemotherapy.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically confirmed, unresectable locally advanced or metastatic transitional cell carcinoma of the urothelium
Stage IV disease at the start of first-line chemotherapy
Measurable disease (per RECIST v1.1) prior to the start of first-line chemotherapy
Prior first-line chemotherapy must have consisted of at least 4 cycles and no more than 6 cycles of gemcitabine + cisplatin and/or gemcitabine + carboplatin
No evidence of progressive disease following completion of first-line chemotherapy (i.e., ongoing CR, PR, or SD per RECIST v1.1 guidelines )

Exclusion Criteria:

Prior adjuvant or neoadjuvant systemic therapy within 12 months of randomization
Prior immunotherapy with IL-2, IFN-α, or an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or CTLA 4 antibody (including ipilimumab), or any other antibody or drug specifically targeting T-cell co-stimulation or immune checkpoint pathways
Persisting toxicity related to prior therapy (Grade >1 NCI CTCAE v4.0); however, alopecia, sensory neuropathy (Grade 2 or less), or other (Grade 2 or less) adverse events not constituting a safety risk based on the investigator's judgement are acceptable.
Patients with known symptomatic central nervous system (CNS) metastases requiring steroids
Diagnosis of any other malignancy within 5 years prior to randomization, except for adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the breast or of the cervix, low grade prostate cancer on surveillance without any plans for treatment intervention, or prostate cancer that has been adequately treated with prostatectomy or radiotherapy and currently with no evidence of disease or symptoms.

Study is for people with:

Bladder Cancer

Phase:

Phase 3

Estimated Enrollment:

700

Study ID:

NCT02603432

Recruitment Status:

Completed

Sponsor:

Pfizer

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Study is for people with:

Bladder Cancer

Phase:

Phase 3

Estimated Enrollment:

700

Study ID:

NCT02603432

Recruitment Status:

Completed

Sponsor:


Pfizer

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