A Phase 1/2 Open-Label, Umbrella Platform Design Study of Investigational Agents in Combination With Pembrolizumab (MK-3475) With or Without Chemotherapy in Participants With 1L Locally Advanced Unresectable/Metastatic Esophageal Cancer: KEYMAKER-U06 Substudy 06E

Status: Recruiting
Location: See all (16) locations...
Intervention Type: Drug, Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

Researchers are looking for new ways to treat esophageal squamous cell carcinoma (ESCC). ESCC is a type of cancer that starts in certain cells that line the esophagus. The esophagus is the tube that connects the throat to the stomach. This study will look at ESCC that is either locally advanced unresectable, which means it has spread into tissue near where it started and cannot be completely removed by surgery, or metastatic, which means it has spread to other body parts. Available treatments for these types of ESCC include pembrolizumab and chemotherapy. Pembrolizumab is an immunotherapy, which is a treatment that helps the immune system fight cancer. Chemotherapy is medicine that destroys cancer cells or stops them from growing. Researchers want to learn about giving pembrolizumab and ifinatamab deruxtecan (I-DXd), a study medicine, with or without chemotherapy to treat ESCC. I-DXd is an antibody-drug conjugate (ADC). An ADC attaches to a protein on cancer cells and delivers treatment to destroy those cells. The main goal of this study is to learn about the safety of I-DXd and pembrolizumab with or without chemotherapy and if people tolerate them. Researchers also want to learn how cancer responds (gets smaller or goes away) to the study treatments.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

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

• Has histologically or cytologically confirmed diagnosis of locally advanced unresectable or metastatic squamous cell carcinoma of the esophagus in first-line (1L) setting.

• Has measurable disease per RECIST 1.1 as assessed by the local site. investigator/radiology assessment and verified by BICR. Lesions situated in a previously irradiated area are considered measurable if progression has been shown in such lesions.

• Has AEs due to previous anticancer therapies of ≤Grade 1 or baseline (except alopecia and vitiligo). Endocrine-related AEs adequately treated with hormone replacement are acceptable.

• Human immunodeficiency virus (HIV)-infected participants must have well controlled HIV on antiretroviral therapy (ART).

• Participants who are hepatitis B surface antigen (HBsAg) positive are eligible if they have received hepatitis B virus (HBV) antiviral therapy for at least 4 weeks, and have undetectable HBV viral load.

• Participants with history of hepatitis C virus (HCV) infection are eligible if HCV viral load is undetectable.

• Has Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.

Locations
Other Locations
China
Beijing Cancer Hospital ( Site 9500)
RECRUITING
Beijing
The Second Affiliated Hospital of Anhui Medical University ( Site 9511)
RECRUITING
Hefei
The First Affiliated Hospital of Nanchang University ( Site 9505)
RECRUITING
Nanchang
The First Affiliated Hospital of Xiamen University ( Site 9503)
RECRUITING
Xiamen
Xuzhou Central Hospital ( Site 9512)
RECRUITING
Xuzhou
Henan Cancer Hospital ( Site 9509)
RECRUITING
Zhengzhou
France
CHU Lille - Institut Coeur Poumon ( Site 9100)
RECRUITING
Lille
Japan
National Cancer Center Hospital ( Site 9700)
RECRUITING
Chūō
National Cancer Center Hospital East ( Site 9701)
RECRUITING
Kashiwa
Aichi Cancer Center ( Site 9702)
RECRUITING
Nagoya
Norway
Oslo Universitetssykehus Radiumhospitalet ( Site 1501)
RECRUITING
Oslo
Republic of Korea
Asan Medical Center ( Site 9901)
RECRUITING
Seoul
Switzerland
Kantonsspital Graubuenden ( Site 1700)
RECRUITING
Chur
Taiwan
National Cheng Kung University Hospital ( Site 1001)
RECRUITING
Tainan City
National Taiwan University Hospital ( Site 1000)
RECRUITING
Taipei
Taipei Veterans General Hospital ( Site 1005)
RECRUITING
Taipei
Contact Information
Primary
Toll Free Number
Trialsites@msd.com
1-888-577-8839
Time Frame
Start Date: 2025-07-30
Estimated Completion Date: 2032-01-04
Participants
Target number of participants: 228
Treatments
Active_comparator: Pembrolizumab + Chemotherapy
Participants will receive 200 mg of pembrolizumab via intravenous (IV) infusion every three weeks (Q3W) on Day 1 of each 21 day cycle up to 35 cycles (up to approximately 2 years), and mFOLFOX6 chemotherapy: oxaliplatin 85 mg/m\^2 via IV infusion every 2 weeks (Q2W) until progressive disease (PD) or toxicity; leucovorin 400 mg/m2 OR levoleucovorin 200 mg/m\^2 via IV infusion Q2W until PD or toxicity; 5-fluorouracil (5-FU) 400 mg/m\^2 bolus IV infusion followed by 2400 mg/m\^2 continuous 46-48 hour IV infusion Q2W until PD or toxicity.
Experimental: Pembrolizumab + I-DXd
Participants will receive 200 mg of pembrolizumab via IV infusion Q3W on Day 1 of each 21 day cycle for up to 35 cycles (up to approximately 2 years). Participants will also receive up to 12 mg/kg I-XDd Q3W via IV infusion until PD or toxicity.
Experimental: Pembrolizumab + I-DXd + 5-FU IV + Leucovorin or Levoleucovorin
Participants will receive 200 mg pembrolizumab via IV infusion Q3W on Day 1 of each 21 day cycle up to 35 cycles (up to approximately 2 years). Participants will also receive I-DXd up to 12 mg/kg via IV infusion Q3W until PD or toxicity, 5-FU 400 mg/m\^2 bolus IV infusion followed by 2400 mg/m\^2 continuous 46-48 hour IV infusion Q2W until PD or toxicity, and leucovorin 400 mg/m\^2 OR levoleucovorin 200 mg/m\^2 via IV infusion Q2W until PD or toxicity.
Experimental: Pembrolizumab + I-DXd + 5-FU IV + Leucovorin or Levoleucovorin + Oxaliplatin
Participants will receive 200 mg of pembrolizumab via IV infusion Q3W on Day 1 of each 21 day cycle up to 35 cycles (up to approximately 2 years). Participants will also receive up to 12 mg/kg I-DXd via IV infusion q3w until PD or toxicity, 5-FU 2400 mg/m\^2 continuous 46-48 hour IV infusion Q2W until PD or toxicity, 60mg/m\^2 oxaliplatin via IV infusion Q2W until PD or toxicity, and leucovorin 400 mg/m\^2 OR levoleucovorin 200 mg/m\^2 via IV infusion Q2W until PD or toxicity.
Related Therapeutic Areas
Sponsors
Collaborators: Daiichi Sankyo
Leads: Merck Sharp & Dohme LLC

This content was sourced from clinicaltrials.gov