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Trial · NCT00277355

Pilot Study of Minocycline in Huntington's Disease

NCT00277355, Phase 2, Phase 3, Completed, Merit Cudkowicz; results first posted 2013-04-19

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pilot Study of Minocycline in Huntington's Disease. Trials, record NCT00277355. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00277355

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Pilot Study of Minocycline in Huntington's Disease
NCT number
NCT00277355
Status
Completed
Phases
Phase 2, Phase 3
Enrollment
114 participants, actual
Lead sponsor
Merit Cudkowicz
Conditions
Huntington Disease
Interventions
minocycline, Matching placebo
First posted
2006-01-16
Last updated
2013-04-19
Results first posted
2013-04-19

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [LOCF Imputation Method]Baseline to 18 months
Establish preliminary estimate of minocycline's impact on progression of HD (measured by the change in Total Functional Capacity (TFC) score of Unified Huntington's Disease Rating Scale \[UHDRS\] between baseline \& Month 18), and to assess futility of further study of minocycline. TFC consists of five ordinally scaled items assessing a person's capacity with: 1. occupation 2. financial affairs 3. domestic responsibilities 4. activities of daily living and 5. independent living. Total score ranges from zero (worst) to 13 (best).
SecondaryChange From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [Regression Based Multiple Imputation Method]Baseline to 18 months
TFC consists of five ordinally scaled items assessing a person's capacity with: (1) occupation; (2) financial affairs; (3) domestic responsibilities; (4) activities of daily living; and (5) independent living. Total score ranges from zero (worst) to 13 (best). Regression based imputation was used to impute missing values.

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [LOCF Imputation Method]Baseline to 18 months
The primary analyses were performed according to the intent to treat principle and included all randomized subjects. Two strategies were used to address missing data: 1. Last observation carried forward (LOCF) was used to impute missing values and 2. A secondary method of regression-based multiple imputation was also used.
units on a scaleMEAN
SECONDARYChange From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [Regression Based Multiple Imputation Method]Baseline to 18 months
The primary analyses were performed according to the intent to treat principle and included all randomized subjects. Two strategies were used to address missing data: 1. Last observation carried forward (LOCF) was used to impute missing values and 2. A secondary method of regression-based multiple imputation was also used.
units on a scaleMEAN

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [LOCF Imputation Method]Minocycline 100 mg Twice Daily1.55Standard Deviation 1.85units on a scale
Change From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [LOCF Imputation Method]Matching Placebo Twice Daily1.15Standard Deviation 1.70units on a scale
Change From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [Regression Based Multiple Imputation Method]Minocycline 100 mg Twice Daily1.71Standard Deviation 1.96units on a scale
Change From Baseline to Month 18 in the Total Functional Capacity (TFC) Scale [Regression Based Multiple Imputation Method]Matching Placebo Twice Daily1.15Standard Deviation 1.70units on a scale

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMinocycline 100 mg Twice Daily87
Overall StudySTARTEDMatching Placebo Twice Daily27
Overall StudyCOMPLETEDMinocycline 100 mg Twice Daily73
Overall StudyCOMPLETEDMatching Placebo Twice Daily22
Overall StudyNOT COMPLETEDMinocycline 100 mg Twice Daily14
Overall StudyNOT COMPLETEDMatching Placebo Twice Daily5

Adverse events92

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherDysphagiaGastrointestinal disordersMinocycline 100 mg Twice Daily487
otherDysphagiaGastrointestinal disordersMatching Placebo Twice Daily227
otherNauseaGastrointestinal disordersMinocycline 100 mg Twice Daily787
otherNauseaGastrointestinal disordersMatching Placebo Twice Daily027
otherIrritabilityGeneral disordersMinocycline 100 mg Twice Daily587
otherIrritabilityGeneral disordersMatching Placebo Twice Daily127
otherBronchitisInfections and infestationsMinocycline 100 mg Twice Daily087
otherBronchitisInfections and infestationsMatching Placebo Twice Daily227
otherGatrointestional viralInfections and infestationsMinocycline 100 mg Twice Daily287
otherGatrointestional viralInfections and infestationsMatching Placebo Twice Daily227

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMinocycline 100 mg Twice Daily
Total, all-cause mortalityMatching Placebo Twice Daily
Total, other adverse eventsMinocycline 100 mg Twice Daily7487
Total, other adverse eventsMatching Placebo Twice Daily2327
Total, serious adverse eventsMinocycline 100 mg Twice Daily1187
Total, serious adverse eventsMatching Placebo Twice Daily127

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
15304592BACKGROUND

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Minocycline 100 mg Twice Daily vs Matching Placebo Twice Daily: serious adverse events

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00277355

GET https://conductscience.org/api/trials/v1/NCT00277355/events?page=2