Clinical Trials in Italy / NCT06483334
Active, not recruiting
Phase 1/2
A Study of Efficacy and Safety of Sacituzumab Tirumotecan (MK-2870) Plus Enfortumab Vedotin (EV) With and Without Pembrolizumab in Advanced Urothelial Carcinoma (MK-3475-04C/KEYMAKER-U04)
NCT06483334 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Metastatic Urothelial CarcinomaLocally Advanced Urothelial Carcinoma
Investigational drug(s) / intervention(s)
Sacituzumab tirumotecan: IV infusion at different dose levels
Enfortumab Vedotin: IV infusion at different dose levels
Pembrolizumab: 200 mg IV infusion
Supportive care measures: Participants are allowed to take supportive care measures at the discretion of the investigator. Prophylactic supportive care measures may include but are not limited to antiemetic agents, antidiarrheal agents, granulocyte and erythroid growth factors, and blood transfusions.
Study summary
This study is a substudy being conducted under one pembrolizumab umbrella master study KEYMAKER-U04. The substudy will consist of 2 parts. Part 1 will evaluate the safety and preliminary efficacy of sacituzumab tirumotecan plus enfortumab vedotin (EV). Part 2 will be based on Part 1 results and will evaluate the efficacy, pharmacokinetics, and safety of sacituzumab tirumotecan plus EV in combination with pembrolizumab in participants with advanced urothelial carcinoma.
Eligibility
Inclusion Criteria:
The main inclusion criteria include but are not limited to the following:
* Must have histologically documented, locally advanced/metastatic urothelial carcinoma (la/mUC).
* Must provide an archival tumor tissue sample or newly obtained core or excisional biopsy of a tumor lesion demonstrating UC, not previously irradiated, and adequate for biomarker evaluation. A newly obtained biopsy is strongly preferred, but not required if archival tissue is evaluable.
* Any AEs due to previous anticancer therapies must have recovered to ≤Grade 1 or baseline. Endocrine-related AEs adequately treated with hormone replacement are eligible.
* PART 1 ONLY: Participants must have received platinum-based chemotherapy for treatment of la/mUC.
* PART 1 ONLY: Participants must not have received \>2 lines of therapy for la/mUC. Platinum-based chemotherapy followed by avelumab maintenance is considered 2 lines of therapy.
* PART 2 ONLY: Participants must not have received prior systemic therapy for la/mUC.
Exclusion Criteria:
The main exclusion criteria include but are not limited to the following:
* Known additional malignancy that is progressing or has required active treatment within the past 3 years.
* Known active central nervous system metastases and/or carcinomatous meningitis.
* Has Grade ≥2 peripheral neuropathy.
* Has history of documented severe dry eye syndrome, severe Meibomian gland disease and/or blepharitis, or severe corneal disease that prevents/delays corneal healing.
* Has active inflammatory bowel disease requiring immunosuppressive medication or previous history of inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis, or chronic diarrhea).
* Has uncontrolled, significant cardiovascular disease or cerebrovascular disease and/or serious cardiovascular and cerebrovascular diseases within the 6 months preceding study intervention.
* Has active keratitis or corneal ulcerations. Superficial punctate keratitis is allowed if the disorder is being adequately treated in the opinion of the investigator.
* Has a history of uncontrolled diabetes.
* Has received an investigational agent or has used an investigational device within 4 weeks prior to study intervention administration.
* Has received a live or live-attenuated vaccine within 30 days prior to the first dose of study intervention.
* PART 2 ONLY: Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days before the first dose of study intervention. Inhaled or topical steroids are permitted in the absence of active autoimmune disease. Physiologic replacement doses of corticosteroids are permitted for participants with adrenal insufficiency.
* PART 2 ONLY: Has an active autoimmune disease that has required systemic treatment in past 2 years except replacement therapy.
* Is human immunodeficiency virus (HIV)-infected and has a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease.
* Has active Hepatitis B or Hepatitis C virus infection.
* Has a history of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease.
* Has an active infection requiring systemic therapy.
* PART 2 ONLY: History of allogeneic tissue/solid organ transplant.
* Has not adequately recovered from major surgery or has ongoing surgical complications.
Primary outcome measure(s)
- Part 1: Percentage of Participants with Dose-limiting toxicities (DLT) — Up to 21 days
A DLT is defined as an event with toxicity including the type, severity, time of onset, time of resolution, and the probable association with study treatment that are not due to pre-existing conditions as defined by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events, Version 5.0 (CTCAE 5.0). The number of participants who experience a DLT in Part 1 will be reported. - Part 1: Percentage of Participants Who Experienced At Least One Adverse Event (AE) — Up to ~3 years
An AE is defined as any untoward medical occurrence in a participant administered study drug, which does not necessarily have to have a causal relationship with the study drug. The number of participants experiencing an AE in Part 1 will be reported. - Part 1: Percentage of Participants Who Discontinued Study Treatment Due to an AE — Up to ~2 years
An AE is defined as any untoward medical occurrence in a participant administered study drug, which does not necessarily have to have a causal relationship with the study drug. The number of participants who discontinue study treatment due to an AE in Part 1 will be reported. - Part 2: Percentage of Participants with DLT — Up to 21 days
A DLT is defined as an event with toxicity including the type, severity, time of onset, time of resolution, and the probable association with study treatment that are not due to pre-existing conditions as defined by the NCI CTCAE 5.0. The number of participants who experience a DLT in Part 2 will be reported. - Part 2: Percentage of Participants Who Experienced At Least One AE — Up to ~3 years
An AE is defined as any untoward medical occurrence in a participant administered study drug, which does not necessarily have to have a causal relationship with the study drug. The number of participants experiencing an AE in Part 2 will be reported. - Part 2: Percentage of Participants Who Discontinued Study Treatment Due to an AE — Up to ~2 years
An AE is defined as any untoward medical occurrence in a participant administered study drug, which does not necessarily have to have a causal relationship with the study drug. The number of participants who discontinue study treatment due to an AE in Part 2 will be reported. - Part 2: Objective Response Rate (ORR) — Up to ~3 years
ORR is defined as the percentage of participants who achieve a confirmed complete response (CR) (disappearance of all target lesions) or partial response (PR) (at least a 30% decrease in the sum of diameters of target lesions) per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 as assessed by investigator. ORR will be reported for participants in Part 2.
Trial sites (25)
| Facility | City | Region | Status |
|---|---|---|---|
| University of California San Francisco HDFCCC ( Site 4044) | San Francisco | California | |
| University of Chicago Medical Center ( Site 4037) | Chicago | Illinois | |
| Indiana University Melvin and Bren Simon Cancer Center ( Site 4011) | Indianapolis | Indiana | |
| Dana-Farber Cancer Institute ( Site 4047) | Boston | Massachusetts | |
| Siteman Cancer Center ( Site 4038) | St Louis | Missouri | |
| Icahn School of Medicine at Mount Sinai ( Site 4018) | New York | New York | |
| Cleveland Clinic-Taussig Cancer Center ( Site 4036) | Cleveland | Ohio | |
| Huntsman Cancer Institute-HCI Clinical Trials Office ( Site 4041) | Salt Lake City | Utah | |
| The Ottawa Hospital - General Campus ( Site 4105) | Ottawa | Ontario | |
| Princess Margaret Cancer Centre ( Site 4106) | Toronto | Ontario | |
| Centre Hospitalier Lyon Sud ( Site 4606) | Pierre-Bénite | Auvergne-Rhône-Alpes | |
| Rambam Health Care Campus ( Site 4501) | Haifa | Israel | |
| Rabin Medical Center-Oncology ( Site 4504) | Petah Tikva | Israel | |
| Sheba Medical Center-ONCOLOGY ( Site 4503) | Ramat Gan | Israel | |
| Ospedale San Raffaele-Oncologia Medica ( Site 4403) | Milan | Lombardy | |
| Fondazione IRCCS Istituto Nazionale dei Tumori ( Site 4405) | Milan | Italy | |
| Istituto Nazionale Tumori IRCCS Fondazione Pascale ( Site 4406) | Naples | Italy | |
| Nederlands Kanker Instituut - Antoni van Leeuwenhoek - NKI-AVL ( Site 4302) | Amsterdam | North Holland | |
| Severance Hospital, Yonsei University Health System-Medical oncology ( Site 4903) | Seoul | South Korea | |
| Asan Medical Center-Department of Oncology ( Site 4901) | Seoul | South Korea | |
| Samsung Medical Center ( Site 4902) | Seoul | South Korea | |
| Hospital Universitari Vall d'Hebron-Oncology ( Site 4767) | Barcelona | Spain | |
| Hospital Clinico San Carlos ( Site 4765) | Madrid | Spain | |
| National Cheng Kung University Hospital-Clinical Trial Center ( Site 4803) | Tainan | Taiwan | |
| St Bartholomew s Hospital ( Site 4206) | London | London, City of |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06483334 on ClinicalTrials.gov ↗ ← All trials in Italy