A Clinical Study of V940 Treatment and Pembrolizumab in People With Bladder Cancer (V940-005/INTerpath-005)

ID#: NCT06305767

Age: 18 years - 66+

Gender: All

Healthy Subjects: No

Study Phase: Phase 1/Phase 2

Recruitment Status: Recruiting

Start Date: March 28, 2024

End Date: April 08, 2031

Contact Information:
Toll Free Number
1-888-577-8839
Summary: Researchers are looking for new ways to treat people with high-risk muscle-invasive urothelial carcinoma (MIUC). Urothelial carcinoma is a type of bladder cancer that begins in cells that line the inside of the bladder and other parts of the urinary tract, such as part of the kidneys, ureters, and urethra. People with MIUC usually have chemotherapy before surgery, then surgery to remove the cancer. Chemotherapy is a type of medicine to destroy cancer cells or stop them from growing. After surgery, some people receive more treatment to prevent cancer from returning. Pembrolizumab is an immunotherapy, which is a treatment that helps the immune system fight cancer. Enfortumab vedotin (EV) is an antibody drug conjugate (ADC). An ADC attaches to a protein on cancer cells and delivers treatment to destroy those cells. Researchers want to learn if giving V940 (the study treatment) with pembrolizumab can prevent MIUC from returning after surgery. V940 (also called mRNA-4157) is designed to treat each person's cancer by helping the person's immune system identify and kill cancer cells based on certain proteins found on those cancer cells. The goals of this study are to learn if people who receive V940 and pembrolizumab are alive and cancer free longer than those who receive placebo and pembrolizumab, and to learn about the safety of V940, pembrolizumab, and EV, and if people tolerate them.
Eligibility:

Inclusion Criteria: The main inclusion criteria include but are not limited to the following:

- Must provide blood samples per protocol, to enable V940 production, and circulating tumor deoxyribonucleic acid testing

- Has an Eastern Cooperative Oncology Group performance status of 0 to 2 assessed within 7 days before randomization

- Must provide a formalin-fixed paraffin-embedded tumor tissue sample for next generation sequencing Adjuvant Cohort:

- Has MIUC

- Has dominant histology of urothelial carcinoma (UC)

- Has high-risk pathologic disease after radical resection

- For participants who have not received cisplatin-based neoadjuvant chemotherapy, are ineligible to receive cisplatin according to protocol pre-defined criteria Perioperative Cohort:

- Has MIBC

- Has a histological diagnosis of UC

- Is deemed eligible for RC and PLND and agrees to undergo curative intent standard RC and PLND and neoadjuvant and adjuvant treatment per protocol

- Is ineligible to receive cisplatin according to protocol pre-defined criteria

Exclusion Criteria: The main exclusion criteria include but are not limited to the following:

- Has received a live or live-attenuated vaccine within 30 days before the first dose of study intervention

- Has known additional malignancy that is progressing or has required active treatment ≤3 years prior to study randomization

- Has current pneumonitis/interstitial lung disease

- Has active infection requiring systemic therapy

- Has active hepatitis B and hepatitis C virus infection Adjuvant Cohort:

- Has received prior systemic anticancer therapy

- Has received prior neoadjuvant therapy, with the exception of neoadjuvant cisplatin-based chemotherapy for MIUC

- Has severe hypersensitivity to either V940 or pembrolizumab (MK-3475) and/or any of their excipients Perioperative Cohort:

- Has received any prior systemic treatment, cancer vaccine treatment, chemoradiation, and/or radiation therapy treatment for MIBC

- Has severe hypersensitivity to either V940, pembrolizumab, or EV and/or any of their excipients

- Has ongoing sensory or motor neuropathy

- Has active keratitis or corneal ulcerations
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