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A Phase 1b/2 Open-label Study Evaluating Different MK-6070 and Ifinatamab Deruxtecan (MK-2400)-Based Regimens in First-line Extensive Stage Small Cell Lung Cancer

Status: Recruiting
Location: See all (13) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

Researchers are looking for new ways to treat extensive-stage small cell lung cancer (ES-SCLC). ES-SCLC is a type of lung cancer that has spread throughout the lung, to the other lung, or to other parts of the body. A standard (usual) treatment for ES-SCLC uses both chemotherapy and immunotherapy. * Chemotherapy is a treatment that works to destroy cancer cells or stop them from growing. * Immunotherapy is a treatment that helps the immune system fight cancer. Gocatamig and I-DXd (short for ifinatamab deruxtecan) are study medicines. Researchers want to know if giving gocatamig and I-DXd together can treat ES-SCLC. Researchers will also look at giving the study medicines with standard treatment. Gocatamig is a T-cell engager therapy. I-DXd is an antibody drug conjugate. * T-cell engager therapy is a certain type of immunotherapy that uses T-cells to find and destroy cancer cells. * A T-cell is a type of white blood cell, which are cells that help the body fight infection. * An antibody drug conjugate (ADC) is a treatment that attaches to a protein on cancer cells and delivers treatment to destroy those cells. The goals of this study are to learn: * About the safety of combining gocatamig and I-DXd and if people tolerate them together * If people who receive gocatamig and I-DXd have ES-SCLC respond, which means the cancer gets smaller or goes away

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 a histologically or cytologically confirmed diagnosis of extensive-stage small cell lung cancer (ES-SCLC)

• For participants receiving gocatamig + ifinatamab deruxtecan (I-DXd) in maintenance only:

‣ Completed 3 to 4 cycles of platinum + etoposide chemotherapy with concurrent approved anti-programmed cell death 1/Ligand 1 (anti PD-1/L1) as first line (1L) treatment of ES-SCLC within 6 weeks prior to enrollment

⁃ No radiological disease progression per Response Evaluation Criteria In Solid Tumors version 1.1 (RECIST 1.1)

⁃ No other prior systemic ES-SCLC therapy allowed

⁃ Rechallenge therapy counts as an additional line and leads to exclusion

• For participants receiving gocatamig + I-DXd in induction and maintenance, or gocatamig + I-DXd in induction followed by gocatamig + atezolizumab in maintenance, or carboplatin + etoposide + atezolizumab in induction followed by atezolizumab in maintenance: No prior systemic ES-SCLC treatment allowed

• Applicable to all participants: prior limited-stage small cell lung cancer (SCLC) is allowed if \> 6 months have passed since the end of previous therapy and progression

• Must be able to provide a pretreatment archival tumor tissue sample or newly obtained core, incisional, or excisional biopsy of a tumor lesion not previously irradiated

• Measurable disease by RECIST 1.1 as assessed by the local site investigator/radiology. Lesions situated in a previously irradiated area are considered measurable if growth has been shown in such lesions since the completion of radiation

Locations
United States
Florida
Orlando Health Cancer Institute ( Site 0108)
RECRUITING
Orlando
Kentucky
Saint Elizabeth Medical Center Edgewood ( Site 0112)
RECRUITING
Edgewood
New Jersey
John Theurer Cancer Center at Hackensack University Medical Center ( Site 0101)
RECRUITING
Hackensack
Tennessee
The University of Tennessee Medical Center ( Site 0120)
RECRUITING
Knoxville
SCRI Oncology Partners ( Site 7000)
RECRUITING
Nashville
Other Locations
China
Beijing Cancer Hospital ( Site 1604)
RECRUITING
Beijing
Shanghai East Hospital ( Site 1600)
RECRUITING
Shanghai
Taizhou Hospital of Zhejiang Province ( Site 1601)
RECRUITING
Taizhou
Israel
Rambam Health Care Campus ( Site 0602)
RECRUITING
Haifa
Sheba Medical Center ( Site 0601)
RECRUITING
Ramat Gan
Republic of Korea
Asan Medical Center ( Site 1404)
RECRUITING
Seoul
Samsung Medical Center ( Site 1401)
RECRUITING
Seoul
Seoul National University Hospital ( Site 1402)
RECRUITING
Seoul
Contact Information
Primary
Toll Free Number
Trialsites@msd.com
1-888-577-8839
Time Frame
Start Date: 2026-01-29
Estimated Completion Date: 2030-12-30
Participants
Target number of participants: 170
Treatments
Experimental: Arm 1, Parts A and B: Gocataming + I-DXd
Participants who completed standard of care (SOC) induction chemotherapy with concurrent approved anti-programmed cell death 1/ligand 1 protein (anti-PD-1/L1) treatment for ES-SCLC and did not have disease progression per investigator discretion, will receive gocatamig and I-DXd in the maintenance phase, until documented disease progression or meeting other study discontinuation criteria.
Experimental: Arm 2, Parts A and B: Gocataming + I-DXd
Participants who did not receive prior systemic treatment for ES-SCLC will receive gocatamig and I-DXd during induction and maintenance phases, until documented disease progression or meeting other study discontinuation criteria.
Experimental: Arm 3, Part B: Gocataming + I-DXd → gocatamig + atezolizumab
Participants who did not receive prior systemic treatment for ES-SCLC will receive gocatamig and I-DXd in the induction phase, followed by gocatamig and atezolizumab in the maintenance phase, until documented disease progression or meeting other study discontinuation criteria.
Active_comparator: Arm 4, Part B: Carboplatin + etoposide + atezolizumab → atezolizumab
Participants who did not receive prior systemic treatment for ES-SCLC will receive SOC (carboplatin + etoposide + atezolizumab) in the induction phase, followed by atezolizumab in the maintenance phase, until documented disease progression or meeting other study discontinuation criteria.
Sponsors
Collaborators: Daiichi Sankyo
Leads: Merck Sharp & Dohme LLC

This content was sourced from clinicaltrials.gov

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