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COMPLETED Phase 1

Clinical Trial of ARQ 761 in Advanced Solid Tumors

NCT01502800 · View on ClinicalTrials.gov ↗

Study Summary

Primary Objective: To determine the safety, tolerability and recommended Phase 2 dose (RP2D) of ARQ 761 administered intravenously. Secondary Objectives: To determine the pharmacokinetic profile of ARQ 761 To assess the preliminary anti-tumor activity of aRQ 761

Conditions Studied

Interventions

  • DRUG ARQ 761
  • DRUG ARQ 761 Weekly Administration
  • DRUG Bi-Weekly Administration of ARQ 761
  • DRUG Two Consecutive Weeks Administration of ARQ 761 with one week of rest

Study Locations (1)

Texas

  • UT Southwestern Medical Center - Simmons Cancer Center — Dallas

Trial Details

FieldValue
Enrollment Target 91 participants
Start Date 2011-12-29
Est. Completion 2019-03
Phase Phase 1

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01502800

The ClinicalTrials.gov registry entry for NCT01502800 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 91 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Texas Southwestern Medical Center, which has 742 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 Solid Tumors appearing as the primary indexed condition, and to 4 interventions — of which ARQ 761 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: NCT01502800 reports 1 study location spanning 1 distinct geographic area — top geographies include 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 NCT01502800 about?

NCT01502800 is a clinical study titled "Clinical Trial of ARQ 761 in Advanced Solid Tumors". Primary Objective: To determine the safety, tolerability and recommended Phase 2 dose (RP2D) of ARQ 761 administered intravenously. Secondary Objectives: To determine the pharmacokinetic profile of ARQ 761 To assess the preliminary anti-tumor activity of aRQ 761

What is the current status of trial NCT01502800?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 91 participants. The study started on 2011-12-29. Estimated completion is 2019-03.

What conditions does trial NCT01502800 study?

This clinical trial studies the following conditions: 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 NCT01502800?

The interventions under investigation include: ARQ 761 (DRUG), ARQ 761 Weekly Administration (DRUG), Bi-Weekly Administration of ARQ 761 (DRUG), Two Consecutive Weeks Administration of ARQ 761 with one week of rest (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01502800?

This trial is sponsored by University of Texas Southwestern Medical Center, which has 742 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01502800 being conducted?

This trial has 1 study location across Texas. 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