Study on MK-6070 for Advanced Cancers with DLL3 Expression
Sponsor: Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Sponsor score: 0
ClinicalTrials ID:NCT04471727
This clinical trial is exploring the safety and effectiveness of a new drug, MK-6070, alone and in combination with other treatments, for patients with advanced cancers that express a protein called DLL3.
Patient Parameters
| Parameter | Options |
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Program Overview
The purpose of this study is to find the best dose and evaluate the safety and effectiveness of MK-6070, a new drug being tested for advanced cancers that have a protein called DLL3. The study will also look at how MK-6070 works when used with other treatments like Atezolizumab and I-DXd.
Eligibility Criteria
Inclusion Criteria
- Have a confirmed diagnosis of cancer that expresses the DLL3 protein.
- Have small cell lung cancer (SCLC) that has returned or not responded to at least one previous treatment, including platinum-based chemotherapy.
- Have Neuroendocrine Prostate Cancer (NEPC) that has returned or not responded to standard treatments.
- Have other high-grade neuroendocrine tumors that:
- Have returned or not responded to standard treatments.
- Do not have a standard treatment available.
- Are not suitable for standard treatment as decided by the doctor.
- Must be able to provide a previous or new tissue sample for testing.
Exclusion Criteria
- Have untreated cancer that has spread to the brain or spinal cord.
- Have a type of brain cancer or other primary brain tumors.
- Have spinal cord compression or uncontrolled disease around the spine.
- Have a history of bleeding in the brain or spinal cord.
- Have active neurological conditions related to cancer.
- Have uncontrolled fluid buildup around the lungs, heart, or abdomen that needs frequent drainage.
- Have a history of autoimmune diseases or immune deficiencies, such as lupus or rheumatoid arthritis.
- Are currently taking medications that suppress the immune system, like high-dose steroids, within two weeks before starting the study.
- Have had significant heart disease or stroke within the last six months.
- Have active hepatitis A, B, or C infections, unless well-controlled.
- Have uncontrolled HIV infection, unless well-controlled.
- Have had a stem cell or organ transplant.
- Have taken immune-boosting drugs like interferon within four weeks before starting the study.
- Have had severe allergic reactions to certain types of antibodies.
- Have a history of lung diseases like pulmonary fibrosis or pneumonitis, unless related to past radiation treatment.
- Have taken another investigational drug within three weeks before starting the study.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Cedar-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute | 90048 | Los Angeles | California |
| University of California San Francisco | 94143 | San Francisco | California |
| University of Colorado | 80045 | Aurora | Colorado |
| Dana Farber Cancer Institute | 02467 | Boston | Massachusetts |
| Karmanos Cancer Center | 48201 | Detroit | Michigan |
| Roswell Park Comprehensive Cancer Center | 14263 | Buffalo | New York |
| Memorial Sloan Kettering Cancer Center | 10021 | New York | New York |
| University Hospitals Cleveland Medical Center | 44106 | Cleveland | Ohio |
| Providence | 97213 | Portland | Oregon |
| Tennessee Oncology | 37203 | Nashville | Tennessee |
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