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NCT02174549 · ClinicalTrials.gov registry record · Phase 1

Dose-defining Study of Tirapazamine Combined With Embolization in Liver Cancer

A Phase 1 study of Hepatocellular Carcinoma and Neuroendocrine Tumors, sponsored by Teclison.

Recruiting
Registry status
Phase 1
Development phase
25
Enrollment target
2
Study locations

NCT02174549 is a Phase 1 study of Hepatocellular Carcinoma and Neuroendocrine Tumors that is actively recruiting participants, run by Teclison. The registered enrollment target is 25 participants, below the 257-participant average among 145 other Hepatocellular Carcinoma trials with a reported enrollment target (90% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT02174549, a Phase 1 study of Hepatocellular Carcinoma and Neuroendocrine Tumors, is actively recruiting participants, sponsored by Teclison.

RECRUITING
Registry status
Phase 1
Development phase
25 participants
Enrollment target
2
Study locations

Study Summary

This phase 1 study is to determine the optimal dose and tolerability of a hypoxia-activating agent, tirapazamine, when it is combined with embolization in liver cancer. Liver cancer patients who are Child-Pugh score A, suitable for embolization with tumor no more than 4 nodules are eligible. Tirapazamine will be given by intra-arterial injection before embolization. Treatment effect is evaluated by MRI based on mRECIST criteria. Repeat treatment is necessary only if disease progression. Dose escalation cohort has been completed. Expansion cohort is open for metastatic liver dominant neuroendocrine tumor.

Interventions

  • DRUG Tirapazamine
  • PROCEDURE Conventional Transarterial Embolization (TAE)

Study Locations (2)

California

  • Stanford University - Palo Alto

Pennsylvania

  • University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2014-09
Est. Completion 2025-12-31
Phase Phase 1

Sponsor

Teclison

4 total trials

What the Registry Record Tells You About NCT02174549

The ClinicalTrials.gov registry entry for NCT02174549 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 257-participant average among 145 other Hepatocellular Carcinoma trials with a reported enrollment target (90% lower). The listed sponsor is Teclison, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Hepatocellular Carcinoma appearing as the primary indexed condition, and to 2 interventions - of which Tirapazamine is the first listed.

NCT02174549 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT02174549 about?

NCT02174549 is a clinical study titled "Dose-defining Study of Tirapazamine Combined With Embolization in Liver Cancer". This phase 1 study is to determine the optimal dose and tolerability of a hypoxia-activating agent, tirapazamine, when it is combined with embolization in liver cancer. Liver cancer patients who are Child-Pugh score A, suitable for embolization with tumor no more than 4 nodules are eligible. Tirapaz...

What is the current status of trial NCT02174549?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2014-09. Estimated completion is 2025-12-31.

What conditions does trial NCT02174549 study?

This clinical trial studies the following conditions: Hepatocellular Carcinoma, Neuroendocrine Tumors, Gastrointestinal Cancer Metastatic.

What interventions are being tested in trial NCT02174549?

The interventions under investigation include: Tirapazamine (DRUG), Conventional Transarterial Embolization (TAE) (PROCEDURE).

Who is sponsoring clinical trial NCT02174549?

This trial is sponsored by Teclison, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02174549 being conducted?

This trial has 2 study locations across California, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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