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NCT02030067 · ClinicalTrials.gov registry record · Phase 1
Dose-Finding and Safety Study for Oral Single-Agent to Treat Advanced Malignancies
A Phase 1 study of Solid Tumor and Metastatic Bladder Cancer, sponsored by Processa Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 127
- Enrollment target
- 12
- Study locations
NCT02030067 is a Phase 1 study of Solid Tumor and Metastatic Bladder Cancer that has completed, run by Processa Pharmaceuticals. The registered enrollment target is 127 participants, below the 221-participant average among 196 other Solid Tumor trials with a reported enrollment target (43% lower). The trial reports 12 study locations across 11 states.
The verdict
NCT02030067, a Phase 1 study of Solid Tumor and Metastatic Bladder Cancer, has completed, sponsored by Processa Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 127 participants
- Enrollment target
- 12
- Study locations
Study Summary
The purpose of this study is to determine the maximum tolerated dose of RX-3117 in subjects with advanced or metastatic solid tumors (Phase 1). The purpose of the Phase 2 portion is to estimate anti-tumor activity in subjects with advanced malignancies (relapsed or refractory pancreatic or advanced bladder cancer).
Conditions Studied
Interventions
- DRUG RX-3117
Study Locations (12)
Florida
- Rexahn Site - Miami
- Rexahn Site - Miami Lakes
Alabama
- Rexahn Site - Birmingham
Arizona
- Rexahn Site - Tucson
California
- Rexahn Site - Duarte
Illinois
- Rexahn Site - Skokie
Missouri
- Rexahn Site - St Louis
Nevada
- Rexahn Site - Las Vegas
New York
- Rexahn Site - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 127 participants |
| Start Date | 2013-12 |
| Est. Completion | 2019-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02030067
The ClinicalTrials.gov registry entry for NCT02030067 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 127 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 221-participant average among 196 other Solid Tumor trials with a reported enrollment target (43% lower). The listed sponsor is Processa Pharmaceuticals, which has 9 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which RX-3117 is the first listed.
NCT02030067 reports 12 study locations spanning 11 distinct geographic areas - top geographies include Florida, Alabama, Arizona.
Frequently Asked Questions
What is clinical trial NCT02030067 about?
NCT02030067 is a clinical study titled "Dose-Finding and Safety Study for Oral Single-Agent to Treat Advanced Malignancies". The purpose of this study is to determine the maximum tolerated dose of RX-3117 in subjects with advanced or metastatic solid tumors (Phase 1). The purpose of the Phase 2 portion is to estimate anti-tumor activity in subjects with advanced malignancies (relapsed or refractory pancreatic or advanced ...
What is the current status of trial NCT02030067?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 127 participants. The study started on 2013-12. Estimated completion is 2019-12.
What conditions does trial NCT02030067 study?
This clinical trial studies the following conditions: Solid Tumor, Metastatic Bladder Cancer.
What interventions are being tested in trial NCT02030067?
The interventions under investigation include: RX-3117 (DRUG).
Who is sponsoring clinical trial NCT02030067?
This trial is sponsored by Processa Pharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02030067 being conducted?
This trial has 12 study locations across Alabama, Arizona, California, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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