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A Study of Emactuzumab and Atezolizumab Administered in Combination in Participants With Advanced Solid Tumors
NCT02323191 · View on ClinicalTrials.gov ↗
Study Summary
This Phase 1, open-label, multicenter, global study will evaluate the safety, pharmacokinetics, and activity of emactuzumab and atezolizumab administered in combination in participants with selected locally advanced or metastatic solid tumors that are not amenable to standard treatment. Participants who receive emactuzumab and atezolizumab will continue to receive study drug as long as they experience clinical benefit in the opinion of the investigator or until unacceptable toxicity or symptomatic deterioration attributed to disease progression as determined by the investigator after an integrated assessment of radiographic data, biopsy results (if available), and clinical status, or withdrawal of consent.
Conditions Studied
Interventions
- DRUG Atezolizumab
- DRUG Emactuzumab
Study Locations (12)
Other
- Cliniques Universitaires St-Luc — Brussels
- Centre Leon Berard; Departement Oncologie Medicale — Lyon
- Institut Claudius Regaud; Departement Oncologie Medicale — Toulouse
- Institut Gustave Roussy; Departement Oncologie Medicale — Villejuif
- Hospital del Mar; Servicio de Oncologia — Barcelona
- Centro Integral Oncológico Clara Campal Ensayos Clínicos START — Madrid
Massachusetts
- Massachusetts General Hospital. — Boston
- Beth Israel Deaconess Medical Center — Boston
- Dana Farber - Harvard — Boston
Connecticut
- Yale Cancer Center; Medical Oncology — New Haven
New York
- Memorial Sloan-Kettering Cancer Center Breast & Imaging Center — New York
Navarre
- Clinica Universitaria de Navarra; Servicio de Oncologia — Pamplona
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 221 participants |
| Start Date | 2015-01-19 |
| Est. Completion | 2020-08-21 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02323191
The ClinicalTrials.gov registry entry for NCT02323191 describes a study currently listed as completed. 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 221 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hoffmann-La Roche, which has 758 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 Solid Cancers appearing as the primary indexed condition, and to 2 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: NCT02323191 reports 12 study locations spanning 5 distinct geographic areas — top geographies include Other, Massachusetts, Connecticut. 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 NCT02323191 about?
NCT02323191 is a clinical study titled "A Study of Emactuzumab and Atezolizumab Administered in Combination in Participants With Advanced Solid Tumors". This Phase 1, open-label, multicenter, global study will evaluate the safety, pharmacokinetics, and activity of emactuzumab and atezolizumab administered in combination in participants with selected locally advanced or metastatic solid tumors that are not amenable to standard treatment. Participant...
What is the current status of trial NCT02323191?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 221 participants. The study started on 2015-01-19. Estimated completion is 2020-08-21.
What conditions does trial NCT02323191 study?
This clinical trial studies the following conditions: Solid Cancers. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02323191?
The interventions under investigation include: Atezolizumab (DRUG), Emactuzumab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02323191?
This trial is sponsored by Hoffmann-La Roche, which has 758 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02323191 being conducted?
This trial has 12 study locations across Connecticut, Massachusetts, New York, Navarre. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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