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COMPLETED Phase 1

A Study to Assess the Safety, Pharmacokinetics and Effectiveness of AGS-16C3F Monotherapy in Subjects With Renal Cell Carcinoma (RCC) of Clear Cell or Papillary Histology

NCT01672775 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety and pharmacokinetics and assess the immunogenicity and effectiveness of AGS-16C3F in subjects with renal cell cancer (RCC).

Interventions

  • DRUG AGS-16C3F

Study Locations (9)

Michigan

  • Site US00005 University of Michigan Medical Center — Ann Arbor
  • Site US00003 Karmanos Cancer Institute — Detroit

New York

  • Site US00004 Roswell Park Cancer Institute — Buffalo
  • Site US00002 Memorial Sloan-Kettering Cancer Center — New York

Washington

  • Site US00001 Seattle Cancer Care Alliance — Seattle

Alberta

  • Site CA00006 Cross Cancer Institute — Edmonton

British Columbia

  • Site CA00008 British Columbia Cancer Agency — Vancouver

Ontario

  • Site CA00009 London Health Sciences Centre — London

Quebec

  • Site CA00007 Jewish General Hospital — Montreal

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2012-07-18
Est. Completion 2017-02-21
Phase Phase 1

Sponsor

Agensys

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01672775

The ClinicalTrials.gov registry entry for NCT01672775 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 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Agensys, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Carcinoma, Renal Cell appearing as the primary indexed condition, and to 1 intervention — of which AGS-16C3F 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: NCT01672775 reports 9 study locations spanning 7 distinct geographic areas — top geographies include Michigan, New York, Washington. 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 NCT01672775 about?

NCT01672775 is a clinical study titled "A Study to Assess the Safety, Pharmacokinetics and Effectiveness of AGS-16C3F Monotherapy in Subjects With Renal Cell Carcinoma (RCC) of Clear Cell or Papillary Histology". The purpose of this study is to evaluate the safety and pharmacokinetics and assess the immunogenicity and effectiveness of AGS-16C3F in subjects with renal cell cancer (RCC).

What is the current status of trial NCT01672775?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2012-07-18. Estimated completion is 2017-02-21.

What conditions does trial NCT01672775 study?

This clinical trial studies the following conditions: Carcinoma, Renal Cell, Renal Cell Carcinoma of Papillary Histology, Renal Cell Carcinoma With Clear Cell Histology, Renal Cell Carcinoma With Non-Clear Cell Histology. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01672775?

The interventions under investigation include: AGS-16C3F (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01672775?

This trial is sponsored by Agensys, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01672775 being conducted?

This trial has 9 study locations across Michigan, New York, Washington, Alberta, British Columbia. 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