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A Study in Participants With Advanced Cancers Associated With Expression of DLL3 (MK-6070-001/HPN328-4001)
NCT04471727 · View on ClinicalTrials.gov ↗
Study Summary
This study will investigate the maximum tolerated dose, the recommended dose for expansion (RDE), safety, efficacy, and pharmacokinetics of gocatamig alone, gocatamig with Atezolizumab and gocatamig with I-DXd in participants with advanced cancers associated with expression of Delta-like Canonical Notch Ligand 3 (DLL3).
Conditions Studied
Interventions
- BIOLOGICAL Atezolizumab
- BIOLOGICAL Gocatamig
- BIOLOGICAL Ifinatamab Deruxtecan (I-DXd)
Study Locations (11)
California
- Cedar-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute — Los Angeles
- University of California San Francisco — San Francisco
New York
- Roswell Park Comprehensive Cancer Center — Buffalo
- Memorial Sloan Kettering Cancer Center — New York
Colorado
- University of Colorado — Aurora
Massachusetts
- Dana Farber Cancer Institute — Boston
Michigan
- Karmanos Cancer Center — Detroit
Ohio
- University Hospitals Cleveland Medical Center — Cleveland
Oregon
- Providence — Portland
Tennessee
- Tennessee Oncology — Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 232 participants |
| Start Date | 2020-12-14 |
| Est. Completion | 2028-01-28 |
| Phase | Phase 1 |
Sponsor
Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)2 total trials
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04471727
The ClinicalTrials.gov registry entry for NCT04471727 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 232 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Neuroendocrine Carcinoma appearing as the primary indexed condition, and to 3 interventions — of which Atezolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04471727 reports 11 study locations spanning 9 distinct geographic areas — top geographies include California, New York, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04471727 about?
NCT04471727 is a clinical study titled "A Study in Participants With Advanced Cancers Associated With Expression of DLL3 (MK-6070-001/HPN328-4001)". This study will investigate the maximum tolerated dose, the recommended dose for expansion (RDE), safety, efficacy, and pharmacokinetics of gocatamig alone, gocatamig with Atezolizumab and gocatamig with I-DXd in participants with advanced cancers associated with expression of Delta-like Canonical N...
What is the current status of trial NCT04471727?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 232 participants. The study started on 2020-12-14. Estimated completion is 2028-01-28.
What conditions does trial NCT04471727 study?
This clinical trial studies the following conditions: Neuroendocrine Carcinoma, Small-Cell Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04471727?
The interventions under investigation include: Atezolizumab (BIOLOGICAL), Gocatamig (BIOLOGICAL), Ifinatamab Deruxtecan (I-DXd) (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04471727?
This trial is sponsored by Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04471727 being conducted?
This trial has 11 study locations across California, Colorado, Massachusetts, Michigan, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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