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NCT02453191 · ClinicalTrials.gov registry record · Phase 1
TVEC and Preop Radiation for Sarcoma (4 ml Dose)
A Phase 1 study of Soft Tissue Sarcoma, sponsored by University of Iowa.
- Completed
- Registry status
- Phase 1
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT02453191 is a Phase 1 study of Soft Tissue Sarcoma that has completed, run by University of Iowa. The registered enrollment target is 30 participants, below the 78-participant average among 55 other Soft Tissue Sarcoma trials with a reported enrollment target (62% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02453191, a Phase 1 study of Soft Tissue Sarcoma, has completed, sponsored by University of Iowa.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research study is to determine the safety and tolerability of talimogene laherparepvec when combined with radiation therapy. Approximately 30 people will take part in this study conducted by investigators at the University of Iowa.
Conditions Studied
Interventions
- RADIATION Radiotherapy
- DRUG Talimogene Laherparepvec
Study Locations (1)
Iowa
- University of Iowa Hospitals and Clinics - Iowa City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2015-07-13 |
| Est. Completion | 2023-03-10 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02453191
The ClinicalTrials.gov registry entry for NCT02453191 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 78-participant average among 55 other Soft Tissue Sarcoma trials with a reported enrollment target (62% lower). The listed sponsor is University of Iowa, which has 228 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Soft Tissue Sarcoma appearing as the primary indexed condition, and to 2 interventions - of which Radiotherapy is the first listed.
NCT02453191 reports 1 study location spanning 1 distinct geographic area - top geographies include Iowa.
Frequently Asked Questions
What is clinical trial NCT02453191 about?
NCT02453191 is a clinical study titled "TVEC and Preop Radiation for Sarcoma (4 ml Dose)". The purpose of this research study is to determine the safety and tolerability of talimogene laherparepvec when combined with radiation therapy. Approximately 30 people will take part in this study conducted by investigators at the University of Iowa.
What is the current status of trial NCT02453191?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2015-07-13. Estimated completion is 2023-03-10.
What conditions does trial NCT02453191 study?
This clinical trial studies the following conditions: Soft Tissue Sarcoma.
What interventions are being tested in trial NCT02453191?
The interventions under investigation include: Radiotherapy (RADIATION), Talimogene Laherparepvec (DRUG).
Who is sponsoring clinical trial NCT02453191?
This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02453191 being conducted?
This trial has 1 study location across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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