Bladder Cancer Clinical Trial

A Study to Evaluate Enfortumab Vedotin Versus (vs) Chemotherapy in Subjects With Previously Treated Locally Advanced or Metastatic Urothelial Cancer (EV-301)

Summary

The purpose of this study was to compare the overall survival (OS) of participants with locally advanced or metastatic urothelial cancer treated with enfortumab vedotin (EV) to the OS of participants treated with chemotherapy.

This study compared progression-free survival on study therapy (PFS1); the overall response rate (ORR) and the disease control rate (DCR) per Response Evaluation Criteria in Solid Tumors (RECIST) V1.1 of participants treated with EV to participants treated with chemotherapy.

In addition, this study evaluated the duration of response (DOR) per RECIST V1.1 of EV and chemotherapy and assessed the safety and tolerability of EV, as well as, the quality of life (QOL) and Patient Reported Outcomes (PRO) parameters.

View Full Description

Full Description

Japan PMDA has approved enfortumab vedotin (Padcev) for the treatment of advanced urothelial cancer. The study will continue as a post marketing study in Japan.

Participants considered an adult according to local regulation at the time of obtaining informed consent participated in the study.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subject is legally an adult according to local regulation at the time of signing informed consent.
Subject has histologically or cytologically confirmed urothelial carcinoma (i.e., cancer of the bladder, renal pelvis, ureter, or urethra). Subjects with urothelial carcinoma (transitional cell) with squamous differentiation or mixed cell types are eligible.
Subject must have experienced radiographic progression or relapse during or after a checkpoint inhibitor (CPI) (anti-programmed cell death protein 1 (PD1) or anti-programmed death-ligand 1 (PD-L1)) for locally advanced or metastatic disease. Subjects who discontinued CPI treatment due to toxicity are eligible provided that the subjects have evidence of disease progression following discontinuation. The CPI need not be the most recent therapy. Subjects for whom the most recent therapy has been a non-CPI based regimen are eligible if the subjects have progressed/relapsed during or after the subjects most recent therapy. Locally advanced disease must not be amenable to resection with curative intent per the treating physician.
Subject must have received a platinum containing regimen (cisplatin or carboplatin) in the metastatic/locally advanced, neoadjuvant or adjuvant setting. If platinum was administered in the adjuvant/neoadjuvant setting subject must have progressed within 12 months of completion.
Subject has radiologically documented metastatic or locally advanced disease at baseline.
An archival tumor tissue sample should be available for submission to central laboratory prior to study treatment. If an archival tumor tissue sample is not available, a fresh tissue sample should be provided. If a fresh tissue sample cannot be provided due to safety concerns, enrollment into the study must be discussed with the medical monitor.
Subject has ECOG PS of 0 or 1

The subject has the following baseline laboratory data:

absolute neutrophil count (ANC) ≥ 1500/mm3
platelet count ≥ 100 × 10^9/L
hemoglobin ≥ 9 g/dL
serum total bilirubin ≤ 1.5 × upper limit of normal (ULN) or ≤ 3 × ULN for subjects with Gilbert's disease
creatinine clearance (CrCl) ≥ 30 mL/min as estimated per institutional standards or as measured by 24 hour urine collection (glomerular filtration rate [GFR] can also be used instead of CrCl)
alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN or ≤ 3 x ULN for subjects with liver metastases

Female subject must either:

Be of nonchildbearing potential: Postmenopausal (defined as at least 1 year without any menses for which there is no other obvious pathological or physiological cause) prior to screening, or documented surgically sterile (e.g., hysterectomy, bilateral salpingectomy, bilateral oophorectomy).
Or, if of childbearing potential: Agree not to try to become pregnant during the study and for at least 6 months after the final study drug administration, and have a negative urine or serum pregnancy test within 7 days prior to Day 1 (Females with false positive results and documented verification of negative pregnancy status are eligible for participation), and if heterosexually active, agree to consistently use a condom plus 1 form of highly effective birth control per locally accepted standards starting at screening and throughout the study period and for at least 6 months after the final study drug administration.
Female subject must agree not to breastfeed or donate ova starting at screening and throughout the study period, and for at least 6 months after the final study drug administration.

A sexually active male subject with female partner(s) who is of childbearing potential is eligible if:

Agrees to use a male condom starting at screening and continue throughout the study treatment and for at least 6 months after final study drug administration. If the male subject has not had a vasectomy or is not sterile as defined below the subjects female partner(s) is utilizing 1 form of highly effective birth control per locally accepted standards starting at screening and continue throughout study treatment and for at least 6 months after the male subject receives final study drug administration.
Male subject must not donate sperm starting at screening and throughout the study period, and for at least 6 months after the final study drug administration.
Male subject with a pregnant or breastfeeding partner(s) must agree to abstinence or use a condom for the duration of the pregnancy or time partner is breastfeeding throughout the study period and for at least 6 months after the final study drug administration.
Subject agrees not to participate in another interventional study while on treatment in present study.

Inclusion Criteria for COE:

Subject is eligible for the COE if they continue to meet all inclusion criteria from the main protocol in addition to the following when the patient is evaluated for eligibility to participate in the COE portion of the study:
Institutional review board (IRB)/ independent ethics committee (IEC) approved written COE informed consent and privacy language as per national regulations (e.g., health insurance portability and accountability act [HIPAA] Authorization for US sites) must be obtained from the subject prior to any study-related procedures (including withdrawal of prohibited medication, if applicable).
Subject was randomized to Arm B and is either currently on study treatment or has discontinued study treatment due to intolerance, AE or progression of disease and has not started a new systemic anticancer treatment.

Exclusion Criteria:

Subject has preexisting sensory or motor neuropathy Grade ≥ 2.

Subject has active central nervous system (CNS) metastases. Subjects with treated CNS metastases are permitted on study if all the following are true:

CNS metastases have been clinically stable for at least 6 weeks prior to screening
If requiring steroid treatment for CNS metastases, the subject is on a stable dose ≤ 20 mg/day of prednisone or equivalent for at least 2 weeks
Baseline scans show no evidence of new or enlarged brain metastasis
Subject does not have leptomeningeal disease
Subject has ongoing clinically significant toxicity (Grade 2 or higher with the exception of alopecia) associated with prior treatment (including systemic therapy, radiotherapy or surgery). Subject with ≤ Grade 2 immunotherapy-related hypothyroidism or panhypopituitarism may be enrolled when well-maintained/controlled on a stable dose of hormone replacement therapy (if indicated). Subjects with ongoing ≥ Grade 3 immunotherapy-related hypothyroidism or panhypopituitarism are excluded. Subjects with ongoing immunotherapy related colitis, uveitis, or pneumonitis or subjects with other immunotherapy related AEs requiring high doses of steroids (> 20 mg/day of prednisone or equivalent) are excluded.
Subject has prior treatment with EV or other monomethyl auristatin E (MMAE)-based Antibody drug conjugates (ADCs).
Subject has received prior chemotherapy for urothelial cancer with all available study therapies in the control arm (i.e., both prior paclitaxel and docetaxel in regions where vinflunine is not an approved therapy, or prior paclitaxel, docetaxel and vinflunine in regions where vinflunine is an approved therapy).
Subject has received more than 1 prior chemotherapy regimen for locally advanced or metastatic urothelial cancer, including chemotherapy for adjuvant or neo-adjuvant disease if recurrence occurred within 12 months of completing therapy. The substitution of carboplatin for cisplatin does not constitute a new regimen provided no new chemotherapeutic agents were added to the regimen.
Subject has history of another malignancy within 3 years before the first dose of study drug, or any evidence of residual disease from a previously diagnosed malignancy. Subjects with nonmelanoma skin cancer, localized prostate cancer treated with curative intent with no evidence of progression, low-risk or very low-risk (per standard guidelines) localized prostate cancer under active surveillance/watchful waiting without intent to treat, or carcinoma in situ of any type (if complete resection was performed) are allowed.
Subject is currently receiving systemic antimicrobial treatment for viral, bacterial, or fungal infection at the time of first dose of EV. Routine antimicrobial prophylaxis is permitted.
Subject has known active Hepatitis B (e.g., hepatitis B surface antigen (HBsAg) reactive) or active hepatitis C (e.g., hepatitis C virus (HCV) Ribonucleic Acid (RNA) [qualitative] is detected).
Subject has known history of human immunodeficiency virus (HIV) infection (HIV 1 or 2).
Subject has documented history of a cerebral vascular event (stroke or transient ischemic attack), unstable angina, myocardial infarction, or cardiac symptoms (including congestive heart failure) consistent with New York Heart Association Class III-IV within 6 months prior to the first dose of study drug.
Subject has radiotherapy or major surgery within 4 weeks prior to first dose of study drug.
Subject has had chemotherapy, biologics, investigational agents, and/or antitumor treatment with immunotherapy that is not completed 2 weeks prior to first dose of study drug.
Subject has known hypersensitivity to EV or to any excipient contained in the drug formulation of EV; OR subject has known hypersensitivity to biopharmaceuticals produced in Chinese hamster ovary (CHO) cells.
Subject has known hypersensitivity to the following: docetaxel or to any of the other excipients listed in product label, including polysorbate 80, paclitaxel or to any of the other excipients listed in product label, such as macrogolglycerol ricinoleate 35 (Ph.Eur.); and vinflunine or to any of the other excipients listed in product label such as other vinca alkaloids (vinblastine,vincristine, vindesine, vinorelbine).
Subject has known active keratitis or corneal ulcerations.
Subject has other underlying medical condition that would impair the ability of the subject to receive or tolerate the planned treatment and follow-up.
History of uncontrolled diabetes mellitus within 3 months of the first dose of study drug. Uncontrolled diabetes is defined as hemoglobin A1C (HbA1c) ≥ 8% or HbA1c between 7 and < 8% with associated diabetes symptoms (polyuria or polydipsia) that are not otherwise explained.

Exclusion Criteria for COE

Subject will be excluded from participation in the COE if they meet any of the exclusion criteria listed in the main protocol or if any of the following apply when the patient is evaluated for eligibility to participate in the COE portion of the study:
Subject has been diagnosed with a new malignancy while on Arm B in the EV-301 study. Subjects with nonmelanoma skin cancer, localized prostate cancer treated with curative intent with no evidence of progression, low-risk or very low-risk (per standard guidelines) localized prostate cancer under active surveillance/watchful waiting without intent to treat, or carcinoma in situ of any type (if complete resection was performed) are allowed.
Subject has already started commercial EV or arrangements have been made for subject to start commercial EV which is reimbursed in their country. Additionally, if EV is commercially available with reimbursement in the potential subject's country, the subject can consider transitioning to the commercial product unless otherwise discussed with sponsor.

Study is for people with:

Bladder Cancer

Phase:

Phase 3

Estimated Enrollment:

608

Study ID:

NCT03474107

Recruitment Status:

Active, not recruiting

Sponsor:

Astellas Pharma Global Development, Inc.

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There are 25 Locations for this study

See Locations Near You

UCI Chao Family Comprehensive Cancer Center
Orange California, 92868, United States
University of California
Sacramento California, 95817, United States
Innovative Clinical Research
Whittier California, 90606, United States
University of Colorado
Denver Colorado, 80045, United States
Smilow Cancer Hospital at Yale-New Haven
New Haven Connecticut, 06510, United States
Sylvester Comprehensive Cancer Center
Miami Florida, 33136, United States
Florida Hospital
Orlando Florida, 32804, United States
Rush University Medical Center
Chicago Illinois, 60612, United States
Norton Cancer Institute
Louisville Kentucky, 40207, United States
Dana-Farber Cancer Institute
Boston Massachusetts, 02215, United States
Nebraska Cancer Specialists
Omaha Nebraska, 68130, United States
Montefiore Medical Center
Bronx New York, 10467, United States
Roswell Park Cancer Institute
Buffalo New York, 14263, United States
Long Island Jewish Medical Center
Lake Success New York, 11042, United States
Sidney Kimmel Center for Prostate and Urologic Cancers
New York New York, 10065, United States
White Plains Hospital Center for Cancer Care - Oncology Site
White Plains New York, 10601, United States
Toledo Clinic Cancer Center
Toledo Ohio, 43623, United States
Providence Portland Med Center
Portland Oregon, 97213, United States
University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States
Fox Chase Cancer Center
Philadelphia Pennsylvania, 19111, United States
Lifespan Rhode Island Hospital
Providence Rhode Island, 02903, United States
Saint Francis Hospital
Greenville South Carolina, 29607, United States
HOPE Cancer Center of East Texas
Tyler Texas, 75701, United States
Benaroya Research Institute at Virginia Mason
Seattle Washington, 98101, United States
Medical College of Wisconsin
Milwaukee Wisconsin, 53226, United States
Site AR54001
Buenos Aires , , Argentina
Site AU61006
Adelaide , , Australia
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Miranda , , Australia
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St. Leonards , , Australia
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Sydney , , Australia
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Linz , , Austria
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Salzburg , , Austria
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Wien , , Austria
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Aalst , , Belgium
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Brussels , , Belgium
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Brussels , , Belgium
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Charleroi , , Belgium
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Gent , , Belgium
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Gent , , Belgium
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Hasselt , , Belgium
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Leuven , , Belgium
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Liège , , Belgium
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Calgary , , Canada
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Edmonton , , Canada
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Montreal , , Canada
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Oshawa , , Canada
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Saskatoon , , Canada
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Sherbrooke , , Canada
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Toronto , , Canada
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Vancouver , , Canada
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Aalborg , , Denmark
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Copenhagen , , Denmark
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Herlev , , Denmark
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Besancon , , France
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Bordeaux , , France
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Bordeaux , , France
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Brest , , France
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Caen , , France
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Lyon , , France
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Marseille , , France
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Nice , , France
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Paris , , France
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Pierre-Bénite , , France
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Saint-Mande , , France
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Strasbourg , , France
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Toulouse , , France
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Villejuif , , France
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Essen , , Germany
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Heidelberg , , Germany
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Münster , , Germany
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Tübingen , , Germany
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Würzburg , , Germany
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Arezzo , , Italy
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Cremona , , Italy
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Milan , , Italy
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Modena , , Italy
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Pisa , , Italy
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Reggio Emilia , , Italy
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Terni , , Italy
Site JP81010
Hirosaki Aomori, , Japan
Site JP81014
Kashiwa Chiba, , Japan
Site JP81007
Sapporo Hokkaido, , Japan
Site JP81026
Sapporo Hokkaido, , Japan
Site JP81020
Tsukuba Ibaraki, , Japan
Site JP81018
Morioka Iwate, , Japan
Site JP81009
Kita-gun Kagawa, , Japan
Site JP81002
Yokohama Kanagawa, , Japan
Site JP81005
Sendai Miyagi, , Japan
Site JP81016
Osakasayama Osaka, , Japan
Site JP81024
Takatsuki Osaka, , Japan
Site JP81008
Bunkyo-ku Tokyo, , Japan
Site JP81012
Koto-ku Tokyo, , Japan
Site JP81013
Shinjuku-ku Tokyo, , Japan
Site JP81011
Ube Yamaguchi, , Japan
Site JP81015
Chiba , , Japan
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Fukuoka , , Japan
Site JP81023
Fukuoka , , Japan
Site JP81004
Hiroshima , , Japan
Site JP81001
Kyoto , , Japan
Site JP81017
Niigata , , Japan
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Okayama , , Japan
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Osaka , , Japan
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Tokushima , , Japan
Site JP81006
Toyama , , Japan
Site KR82006
Daejeon , , Korea, Republic of
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Goyang-Si , , Korea, Republic of
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Hwasun-gun , , Korea, Republic of
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Incheon , , Korea, Republic of
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Seongnam-si , , Korea, Republic of
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Seoul , , Korea, Republic of
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Seoul , , Korea, Republic of
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Seoul , , Korea, Republic of
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Seoul , , Korea, Republic of
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Seoul , , Korea, Republic of
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Shin , , Korea, Republic of
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Amsterdam , , Netherlands
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Amsterdam , , Netherlands
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Nijmegen , , Netherlands
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Tilburg , , Netherlands
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Lisboa , , Portugal
Site PT35102
Lisbon , , Portugal
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Porto , , Portugal
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Ivanovo , , Russian Federation
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Obninsk , , Russian Federation
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Omsk , , Russian Federation
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Vologda , , Russian Federation
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Badajoz , , Spain
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Badalona , , Spain
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Barcelona , , Spain
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Barcelona , , Spain
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Barcelona , , Spain
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Córdoba , , Spain
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Madrid , , Spain
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Madrid , , Spain
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Madrid , , Spain
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Madrid , , Spain
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Manresa , , Spain
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Pamplona , , Spain
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Seville , , Spain
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Valencia , , Spain
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Valencia , , Spain
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Bern , , Switzerland
Site CH41001
Chur , , Switzerland
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Kaohsiung , , Taiwan
Site TW88605
Kaohsiung , , Taiwan
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Taichung , , Taiwan
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Tainan , , Taiwan
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Taipei , , Taiwan
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Taoyuan , , Taiwan
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London , , United Kingdom
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London , , United Kingdom
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Sheffield , , United Kingdom
Site GB44011
Southampton , , United Kingdom
Site GB44013
Sutton , , United Kingdom
Site GB44004
Wirral , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Bladder Cancer

Phase:

Phase 3

Estimated Enrollment:

608

Study ID:

NCT03474107

Recruitment Status:

Active, not recruiting

Sponsor:


Astellas Pharma Global Development, Inc.

How clear is this clinincal trial information?

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