CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 51 enrolled
Drug / intervention
Minocycline +2 moredrug
Likely dose
Minocycline 100 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01636934
NCT01636934Phase 2Completed

A Randomized, Placebo Controlled-Double Blind Study of Minocycline for Reducing the Symptom Burden Produced by Chemoradiation Treatment for Non Small Cell Lung Cancer

M.D. Anderson Cancer Center·interventional·Posted Jul 10, 2012·Updated Jul 17, 2020

In Brief

A Phase 2 clinical trial evaluating Minocycline, Placebo, and 1 other intervention for Lung Cancer. Completed, enrolled 51 participants across 1 site.

Detailed Summary

The goal of this clinical research study is to learn if minocycline can reduce the side effects reported by patients with NSCLC who are receiving chemoradiation therapy. In this study, minocycline will be compared to a placebo. Minocycline is an antibiotic that may help to reduce side effects of chemoradiation therapy. A placebo is not a drug. It looks like the study drug but is not designed to treat any disease or illness. It is designed to be compared with a study drug to learn if the study drug has any real effect.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLung Cancer
CountriesUnited States

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJul 10, 2012
Enrollment StartJul 1, 2012
Primary CompletionSep 23, 2019
TodayJul 2, 2026
Enrollment to primary: 7.2 yearsPosted 14.0 years ago

Interventions

Minocyclinedrug

100 mg by mouth two times a day (200 mg/day) every day for 7 weeks, starting on the first week of chemoradiation therapy.

Placeboother

1 capsule by mouth two times a day every day for 7 weeks, starting on the first week of chemoradiation therapy.

Questionnairesbehavioral

Questionnaires at baseline, timepoints during chemoradiation, and at treatment completion for 12 weeks.