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Clinical Trial of Lurbinectedin (PM01183) in Selected Advanced Solid Tumors
NCT02454972 · View on ClinicalTrials.gov ↗
Study Summary
Multicenter, open-label, exploratory, phase II clinical trial to evaluate the efficacy and safety of PM01183 in previously treated patients with advanced solid tumors
Conditions Studied
Interventions
- DRUG lurbinectedin (PM01183)
Study Locations (20)
Other
- Institut Jules Bordet — Brussels
- Hôpital Cochin — Paris
- Institut Claudius Regaud — Toulouse
- Institut Gustave Roussy — Villejuif
- Charité Universitätsmedizin Berlin - Campus Benjamin Franklin - Comprehensive Cancer Center — Berlin
- Charité - Universitätsmedizin Berlin — Berlin
- Istituto Ortopedico Rizzoli — Bologna
- lstituto Europeo di Oncologia — Milan
- ASST Monza - Ospedale San Gerardo di Monza Struttura Complessa di Oncologia Medica — Monza
- AUSL Romagna - Ospedale Santa Maria delle Croci — Ravenna
Massachusetts
- Massachussets General Hospital — Boston
- Beth Israel Deaconess Medical Centre — Boston
- Dana Farber Cancer Institute — Boston
Texas
- The University of Texas MD Anderson Cancer Center — Houston
- Institute for Drug Development, Cancer Therapy & Research Center at University of Texas Health Science Center — San Antonio
California
- Sarcoma Oncology Research Center, LLC — Santa Monica
Colorado
- University of Colorado Cancer Center — Aurora
Milan
- Istituto Clinico Humanitas — Rozzano
A Coruña
- Complexo Hospitalario Universitario de Santiago — Santiago de Compostela
Guipúzcoa
- Hopsital Universitario Donostia - Donostia Unibertsitate Ospitalea — San Sebastián
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 345 participants |
| Start Date | 2015-08-25 |
| Est. Completion | 2020-09-18 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02454972
The ClinicalTrials.gov registry entry for NCT02454972 describes a study currently listed as completed. It is categorized as Phase 2, 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 345 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is PharmaMar, which has 36 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 Advanced Solid Tumors appearing as the primary indexed condition, and to 1 intervention — of which lurbinectedin (PM01183) 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: NCT02454972 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Other, Massachusetts, Texas. 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 NCT02454972 about?
NCT02454972 is a clinical study titled "Clinical Trial of Lurbinectedin (PM01183) in Selected Advanced Solid Tumors". Multicenter, open-label, exploratory, phase II clinical trial to evaluate the efficacy and safety of PM01183 in previously treated patients with advanced solid tumors
What is the current status of trial NCT02454972?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 345 participants. The study started on 2015-08-25. Estimated completion is 2020-09-18.
What conditions does trial NCT02454972 study?
This clinical trial studies the following conditions: Advanced 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 NCT02454972?
The interventions under investigation include: lurbinectedin (PM01183) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02454972?
This trial is sponsored by PharmaMar, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02454972 being conducted?
This trial has 20 study locations across California, Colorado, Massachusetts, Texas, Milan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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