Gemcitabine and Carboplatin After Progression on Enfortumab Vedotin and Pembrolizumab in Advanced/Metastatic Urothelial Carcinoma

NCT ID: NCT07043972

Last Updated: 2025-07-20

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 55 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-07-09
• Study Completion Date: 2031-01-01

Brief Summary

The goal of this clinical trial is to learn if a chemotherapy combination called gemcitabine and carboplatin (GC) works to treat advanced urothelial cancer in people who have already been treated with enfortumab vedotin and pembrolizumab (EVP).

It will also learn about the efficacy and safety of GC in these patients.

The main questions it aims to answer are:

• Does GC shrink the cancer or stop it from growing?
• What medical side effects do participants have while receiving GC?

Researchers will study how GC affects survival, cancer control, and quality of life. They will also collect blood samples to look at health-related markers and cancer DNA in the blood.

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Participants will:

• Receive the GC chemotherapy (gemcitabine and cisplatin) after having been treated with EVP
• Visit the clinic regularly for checkups, lab tests, and scans
• Answer questions about their health, quality of life, and daily function
• Provide blood samples for research

This study may help researchers find better ways to treat advanced bladder and urinary tract cancer in the future-especially for older adults or those who have already tried other treatments.

Detailed Description

This is a non-randomized single arm, two stage, open-label phase 2 efficacy study in adult patients with locally advanced or metastatic urothelial cancer. Subjects must have had one prior line of therapy consisting of EVP and have RECIST measurable disease prior to study entry. Patients will be treated with standard of care doses of all the chemotherapeutic drugs. Each cycle will consist of gemcitabine 1,000 mg/m2 administered over 30 minutes IV on days 1 and 8, followed by carboplatin AUC 5 on day 1, every 3 weeks. Patients will be treated until disease progression or any of the conditions listed in the protocol applies. Response to treatment will be evaluated by investigator determined CT scan or MRI every 9 weeks and the tumor will be assessed using RECIST v1.1 criteria. The study will be analyzed for futility after treatment of 19 patients. Patients who are not evaluable for the primary endpoint will be replaced.

Conditions

Urothelial Carcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Gemcitabine plus carboplatin

Patients will be treated with gemcitabine 1,000 mg/m2 administered over 30 minutes IV on days 1 and 8, followed by carboplatin area under the curve (AUC) 5 on day 1, every 3 weeks.

Group Type: EXPERIMENTAL

Gemcitabine

Intervention Type: DRUG

IV over 30 minutes given on days 1 and 8 of a 21 day cycle

Carboplatin

Intervention Type: DRUG

IV over 30 minutes given on day 1 of a 21 day cycle

Interventions

Gemcitabine

IV over 30 minutes given on days 1 and 8 of a 21 day cycle

Intervention Type: DRUG

Carboplatin

IV over 30 minutes given on day 1 of a 21 day cycle

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients must have metastatic or locally advanced histologically and radiographically confirmed urothelial carcinoma
• Patients must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension in accordance with RECIST criteria v1.1
• Patients must have received treatment with enfortumab vedotin plus pembrolizumab in the first line setting. Study treatment may be started within 28 days of last treatment with EV-P or with continuing toxicities if considered by the Sponsor-Investigator to be safe and within the best interest of the patient.
• Age > 18 years.
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2
• Patients must have normal organ and marrow function as defined below.

• Absolute neutrophil count > 1,000/mm3 unless patient has constitutional neutropenia
• Platelets > 80,000/ul
• Hemoglobin > 8.0 g/dL
• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) <2.5 x ULN or <3.5 x upper limit of normal (ULN) if liver metastases
• Creatinine Clearance >20 mL/min
• Ability to understand and willingness to sign a written informed consent and HIPAA consent document
• Optional: Archival tumor biospecimen, when available, must be procured for correlative evaluation. If tumor tissue is not available or accessible despite good faith efforts, patient may still be treated on study. Formalin fixed paraffin embedded (FFPE) tissue block(s) or at least 15 unbaked, unstained slides are required. Tissue samples taken from a metastatic lesion prior to the start of screening are acceptable.

Exclusion Criteria

• Patients who have had systemic treatment including EV-P or radiotherapy within 2 weeks prior to entering the study
• Patients who have had systemic treatment including EV-P or radiotherapy within 2 weeks prior to entering the study
• Patients who have received more than one line of prior therapy or prior platinum-based chemotherapy for locally advanced or metastatic urothelial carcinoma (neoadjuvant platinum-based therapy including cisplatin is allowed)
• Patients who have not recovered from adverse events to less than Grade 2 secondary to agents administered more than 2 weeks prior to treatment initiation.
• Patients may not be receiving any other investigational agents
• Patients with uncontrolled and untreated CNS metastases:

• Prior radiation to central nervous system (CNS) metastases is permitted
• Prior history of CNS disease that has responded to previous systemic therapy is permitted only if no recurrence
• Patient should not have leptomeningeal disease
• CNS metastases have been clinically stable for at least 6 weeks prior to screening and baseline scans show no evidence of new or enlarged metastases
• Uncontrolled intercurrent illness including, but not limited to ongoing or active untreated infection, symptomatic congestive heart failure, unstable angina pectoris, symptomatic uncontrolled cardiac arrhythmia, or psychiatric illness/social situations that would limit adherence with study requirements
• Subjects with a history of another invasive malignancy within 3 years before the first dose of study drug that cannot be watched and requires tumor- directed treatment, or any evidence of residual disease from a previously diagnosed malignancy that cannot be watched and requires treatment (adjuvant hormonal therapy for breast cancer is allowed)
• Currently receiving systemic antimicrobial treatment for active infection (viral, bacterial, or fungal) at the time of first dose of chemotherapy (routine antimicrobial prophylaxis is permitted)
• Pregnant or breast feeding.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fox Chase Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Daniel Geynisman, MD

Role: PRINCIPAL_INVESTIGATOR

Fox Chase Cancer Center

Locations

Fox Chase Cancer Center

Philadelphia, Pennsylvania, United States

Site Status: RECRUITING

Temple University Hospital at Broad Street

Philadelphia, Pennsylvania, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Daniel Geynisman, MD

Role: CONTACT

Daniel.Geynisman@fccc.edu

(888) 369-2427

Ryan Romasko, MBA

Role: CONTACT

protocoldev@fccc.edu

(888) 369-2427

Facility Contacts

Daniel Geynisman, MD

Role: primary

Daniel.Geynisman@fccc.edu

888-369-2427

Ryan Romasko, MBA

Role: backup

protocoldev@fccc.edu

(888) 369-2427

Daniel Geynisman, MD

Role: primary

Daniel.Geynisman@fccc.edu

888-369-2427

Ryan Romasko, MBA

Role: backup

protocoldev@fccc.edu

Other Identifiers

25-1008

Identifier Type: OTHER

Identifier Source: secondary_id

GU-230

Identifier Type: -

Identifier Source: org_study_id