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NCT01820299 · ClinicalTrials.gov registry record · Phase 1

Phase I Assay-guided Trial of Anti-inflammatory Phytochemicals in Patients With Advanced Cancer

A Phase 1 study, sponsored by Medical University of South Carolina.

Completed
Registry status
Phase 1
Development phase
22
Enrollment target

NCT01820299: Completed Phase 1 study, sponsored by Medical University of South Carolina.

NCT01820299 is a Phase 1 study that has completed, run by Medical University of South Carolina. The registered enrollment target is 22 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01820299, a Phase 1 study, has completed, sponsored by Medical University of South Carolina.

COMPLETED
Registry status
Phase 1
Development phase
22 participants
Enrollment target

Study Summary

This study is for subjects with solid cancers (gastrointestinal, lung, breast, prostate, lymphoma or cancer of the lymph nodes). The overall goal of this study is to identify plant-derived phytochemicals that can safely reduce systemic inflammation (inflammation throughout the entire body) in subjects with advanced cancer.

Primary Outcome

Decisions to escalate or expand a dose level will be based only on the GSE-only treatment period (day 1-21). To be evaluable for toxicity, a patient must receive at least 3 weeks of GSE treatment, or have experienced dose-limiting toxicity (DLT). All patients enrolled are to be fully followed for toxicity, but any patients who are not evaluable for toxicity will be replaced.

Interventions

  • DRUG Vitamin D
  • DRUG Grape Seed Extract

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2013-03
Est. Completion 2016-05
Phase Phase 1

What the finished NCT01820299 record still lists

NCT01820299 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower).

The record links to 0 conditions, and to 2 interventions - of which Vitamin D is the first listed.

NCT01820299 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01820299 about?

NCT01820299 is a clinical study titled "Phase I Assay-guided Trial of Anti-inflammatory Phytochemicals in Patients With Advanced Cancer". This study is for subjects with solid cancers (gastrointestinal, lung, breast, prostate, lymphoma or cancer of the lymph nodes). The overall goal of this study is to identify plant-derived phytochemicals that can safely reduce systemic inflammation (inflammation throughout the entire body) in subjec...

What is the current status of trial NCT01820299?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2013-03. Estimated completion is 2016-05.

What interventions are being tested in trial NCT01820299?

The interventions under investigation include: Vitamin D (DRUG), Grape Seed Extract (DRUG).

Who is sponsoring clinical trial NCT01820299?

This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01820299's enrollment target sits among peer trials

22 1601st of 2000 higher than 386 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01820299, the US trial registry maintained by the National Library of Medicine. NCT01820299 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.