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COMPLETED Phase 1

Dose-Finding and Safety Study for Oral Single-Agent to Treat Advanced Malignancies

NCT02030067 · View on ClinicalTrials.gov ↗

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).

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

FieldValue
Enrollment Target 127 participants
Start Date 2013-12
Est. Completion 2019-12
Phase Phase 1

Sponsor

Processa Pharmaceuticals

3 total trials

Interested in This Trial?

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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. 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 127 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Processa Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. 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: NCT02030067 reports 12 study locations spanning 11 distinct geographic areas — top geographies include Florida, Alabama, Arizona. 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 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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02030067?

The interventions under investigation include: RX-3117 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02030067?

This trial is sponsored by Processa Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial