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ACTIVE NOT RECRUITING Phase 2

ExIST Study of LY2157299 (Galunisertib) in Rectal Cancer

NCT02688712 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to see how effective and safe LY2157299, in combination with chemotherapy and radiation therapy, might be in treating rectal cancer. Also as part of this study, research will be done on tumor samples to see if it is possible to predict if patients will respond to treatment, and blood samples to look at the immune system response to study treatment. About 50 people will take part in this study. The study treatment will be given over an 8 week period and the investigators will continue to collect your health information for up to 5 years, as part of this study

Conditions Studied

Interventions

  • DRUG Capecitabine
  • DRUG Fluorouracil
  • DRUG LY2157299
  • PROCEDURE Tumor specific mesorectal excision

Study Locations (1)

Oregon

  • Providence Cancer Center — Portland

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2016-03-24
Est. Completion 2025-12
Phase Phase 2

Sponsor

Providence Health & Services

30 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02688712

The ClinicalTrials.gov registry entry for NCT02688712 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Providence Health & Services, which has 30 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 Rectal Adenocarcinoma appearing as the primary indexed condition, and to 4 interventions — of which Capecitabine 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: NCT02688712 reports 1 study location spanning 1 distinct geographic area — top geographies include Oregon. 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 NCT02688712 about?

NCT02688712 is a clinical study titled "ExIST Study of LY2157299 (Galunisertib) in Rectal Cancer". The purpose of this study is to see how effective and safe LY2157299, in combination with chemotherapy and radiation therapy, might be in treating rectal cancer. Also as part of this study, research will be done on tumor samples to see if it is possible to predict if patients will respond to treatme...

What is the current status of trial NCT02688712?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 50 participants. The study started on 2016-03-24. Estimated completion is 2025-12.

What conditions does trial NCT02688712 study?

This clinical trial studies the following conditions: Rectal Adenocarcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02688712?

The interventions under investigation include: Capecitabine (DRUG), Fluorouracil (DRUG), LY2157299 (DRUG), Tumor specific mesorectal excision (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02688712?

This trial is sponsored by Providence Health & Services, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02688712 being conducted?

This trial has 1 study location across Oregon. 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