Enfortumab Vedotin for Advanced Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new cancer treatment called enfortumab vedotin (also known as Padcev) to evaluate its effectiveness against several types of advanced cancers. The primary goal is to measure the treatment's ability to shrink tumors. The trial also assesses the treatment's safety and its impact on patient survival. Individuals with advanced cancers, such as certain types of breast, lung, head and neck, and stomach cancers, who have not responded to standard treatments, might be suitable candidates for this trial. Participants will receive the treatment through an IV infusion on specific days within a treatment cycle. As a Phase 2 trial, the research focuses on assessing the treatment's effectiveness in an initial, smaller group of people.
Do I need to stop my current medications for the trial?
The trial information does not specify if you need to stop taking your current medications. However, it mentions that you should not participate in another interventional study while receiving treatment in this trial. It's best to discuss your current medications with the trial team to get a clear answer.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that enfortumab vedotin, when used alone, has been studied in patients with advanced non-small cell lung cancer. The study found that the treatment was generally well-tolerated. Some patients experienced side effects like tiredness and skin rash, but these were usually manageable.
When combined with pembrolizumab, enfortumab vedotin has also been tested for bladder cancer. Studies have found that this combination reduces certain risks for patients, suggesting it is relatively safe. However, some common side effects included skin reactions and changes in taste.
This trial is in phase 2, indicating that the treatment has shown some safety in earlier studies. More research is needed to confirm its safety. Prospective participants might find these findings helpful in understanding what to expect.12345Why are researchers excited about this trial's treatments?
Enfortumab vedotin is unique because it combines an antibody with a cancer-fighting agent, specifically targeting cancer cells while minimizing damage to healthy cells. Unlike traditional chemotherapy, which can affect both cancerous and healthy cells, enfortumab vedotin is designed to deliver its payload directly to the cancer cells, potentially reducing side effects. Researchers are particularly excited about its potential effectiveness in various cancers, such as breast and lung cancer, especially for patients who may not respond well to existing treatments like standard chemotherapies or targeted therapies. In some cases, like head and neck squamous cell carcinoma, it is used in combination with pembrolizumab, an immunotherapy, which may enhance its effectiveness by helping the immune system recognize and attack cancer cells.
What evidence suggests that this trial's treatments could be effective for advanced cancer?
Research has shown that enfortumab vedotin, which participants in this trial will receive, may be effective against various cancers. Different cohorts in this trial will study its effects on specific cancer types. For stomach and esophagus cancers, studies found that this treatment has promising effects, with patients living an average of 4 to 7 months longer. In hormone receptor-positive breast cancer, enfortumab vedotin showed some positive effects, although it didn't achieve all the trial's goals. In non-small cell lung cancer, both squamous and non-squamous types, some patients responded to the treatment, but these responses were less common. For head and neck cancer, the drug helped 24% of patients who had already tried many other treatments. Lastly, in triple-negative breast cancer, combining enfortumab vedotin with pembrolizumab significantly increased the number of patients who had a complete response compared to surgery alone. Overall, enfortumab vedotin shows potential in treating different types of cancer, offering hope for better outcomes.678910
Who Is on the Research Team?
Medical Director
Principal Investigator
Astellas Pharma Global Development, Inc.
Are You a Good Fit for This Trial?
Adults with various advanced or metastatic cancers (like breast, lung, gastric, and head & neck cancer) who have measurable disease and are in good physical condition (ECOG 0-1). They must have normal organ function tests, no recent second malignancies or severe neuropathy, not be on active infection treatment, and without HIV or hepatitis B/C. Prior treatments should be completed at least 2 weeks before the trial.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive enfortumab vedotin on days 1, 8, and 15 every 28-day cycle for cohorts 1 to 8, and enfortumab vedotin on days 1, 8, and pembrolizumab on day 1 every 21-day cycle for cohort 9
Follow-up
Participants are monitored for safety and effectiveness after treatment with imaging scans every 8 weeks for cohorts 1-8 and every 6 weeks for cohort 9 until disease progression or other criteria are met
Long-term Follow-up
Participants are contacted every 12 weeks for survival status after disease progression or initiation of new therapy
What Are the Treatments Tested in This Trial?
Interventions
- Enfortumab Vedotin
Enfortumab Vedotin is already approved in United States, European Union for the following indications:
- Locally advanced or metastatic urothelial cancer
- Locally advanced or metastatic urothelial cancer
Find a Clinic Near You
Who Is Running the Clinical Trial?
Astellas Pharma Global Development, Inc.
Lead Sponsor
Tadaaki Taniguchi
Astellas Pharma Global Development, Inc.
Chief Medical Officer
M.D., Ph.D.
Naoki Okamura
Astellas Pharma Global Development, Inc.
Chief Executive Officer
Not available
Merck Sharp & Dohme LLC
Industry Sponsor
Chirfi Guindo
Merck Sharp & Dohme LLC
Chief Marketing Officer since 2022
Degree in Engineering from Ecole Centrale de Paris, MBA from New York University Stern School of Business
Robert M. Davis
Merck Sharp & Dohme LLC
Chief Executive Officer since 2021
JD from Northwestern University Pritzker School of Law, MBA from Northwestern University Kellogg Graduate School of Management, Bachelor's in Finance from Miami University
Seagen Inc.
Industry Sponsor
Dr. Roger Dansey
Seagen Inc.
Chief Medical Officer since 2018
MD from University of Witwatersrand
David R. Epstein
Seagen Inc.
Chief Executive Officer since 2022
BSc in Pharmacy from Rutgers University, MBA from Columbia University