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Rollover Study in Participants With Metastatic Solid Tumors Benefiting From Therapy With Sacituzumab Govitecan-hziy
NCT04319198 · View on ClinicalTrials.gov ↗
Study Summary
The goal of this clinical study is to learn more about the study drug, sacituzumab govitecan-hziy (SG), and how safe it is in participants with metastatic cancer (cancer that has spread).
Conditions Studied
Interventions
- DRUG Sacituzumab Govitecan-hiy
Study Locations (20)
Texas
- Next Oncology — Austin
- Oncology Consultants,P.A. — Houston
- The University of Texas M.D. Anderson Cancer Center — Houston
- NEXT Oncology — San Antonio
Other
- Institut Jules Bordet — Brussels
- CHU UCL NAMUR - Sainte Elisabeth — Namur
- Institut Bergonie — Bordeaux
- Centre Leon Berard — Lyon
Florida
- Florida Cancer Specialists & Research Institute — Fort Myers
- Baptist Health - Miami Cancer Institute — Miami
Illinois
- Illinois Cancer Specialists — Arlington Heights
- University of Chicago — Chicago
Massachusetts
- Massachusetts General Hospital — Boston
- Dana Farber Cancer Institute — Boston
California
- University of California San Francisco — San Francisco
Colorado
- Rocky Mountain Cancer Center — Aurora
Delaware
- Christiana Care Health Services, Christiana Hospital — Newark
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2020-08-04 |
| Est. Completion | 2024-10-18 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04319198
The ClinicalTrials.gov registry entry for NCT04319198 describes a study currently listed as completed. It is categorized as Phase 4, 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 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gilead Sciences, which has 190 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Metastatic Solid Tumors appearing as the primary indexed condition, and to 1 intervention — of which Sacituzumab Govitecan-hiy 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: NCT04319198 reports 20 study locations spanning 11 distinct geographic areas — top geographies include Texas, Other, Florida. 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 NCT04319198 about?
NCT04319198 is a clinical study titled "Rollover Study in Participants With Metastatic Solid Tumors Benefiting From Therapy With Sacituzumab Govitecan-hziy". The goal of this clinical study is to learn more about the study drug, sacituzumab govitecan-hziy (SG), and how safe it is in participants with metastatic cancer (cancer that has spread).
What is the current status of trial NCT04319198?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 25 participants. The study started on 2020-08-04. Estimated completion is 2024-10-18.
What conditions does trial NCT04319198 study?
This clinical trial studies the following conditions: Metastatic Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04319198?
The interventions under investigation include: Sacituzumab Govitecan-hiy (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04319198?
This trial is sponsored by Gilead Sciences, which has 190 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04319198 being conducted?
This trial has 20 study locations across California, Colorado, Delaware, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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