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Comparison · NCT02207556-sae

Doxycycline (Localized Disease) vs Doxycycline (Systemic Disease): serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Doxycycline (Localized Disease) vs Doxycycline (Systemic Disease): serious adverse events. Trial comparisons, record NCT02207556-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02207556-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.20.03620.624wilson
Risk in group 20.520.3350.7wilson
Risk difference, group 1 minus group 2-0.32-0.5630.143newcombe hybrid score
Risk ratio, group 1 over group 20.3850.0642.31log
Odds ratio, group 1 over group 20.2310.02252.37log
Number needed to treat, for one fewer participant with a serious adverse event on Doxycycline (Localized Disease) than on Doxycycline (Systemic Disease)3.13from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Doxycycline (Localized Disease)
Doxycycline will be administered at dose of 100mg orally twice daily for 1 year.~Doxycycline: Doxycycline will be continued until one of the following criteria is met:~* Patient has completed 1 year of doxycycline therapy~* Patient develops any grade 3-4 toxicity related to doxycycline use.
15EG000
Group 2Doxycycline (Systemic Disease)
Doxycycline will be administered at dose of 100mg orally twice daily for 1 year.~Doxycycline: Doxycycline will be continued until one of the following criteria is met:~* Patient has completed 1 year of doxycycline therapy~* Patient develops any grade 3-4 toxicity related to doxycycline use.
1325EG001

Harm

What it counts
Total, serious adverse events
Time frame
1 year

Source ClinicalTrials.gov

Trial

Title
Doxycycline to Upgrade Organ Response in Light Chain (AL) Amyloidosis Trial
NCT number
NCT02207556
Phases
PHASE2
Conditions
Primary Systemic Amyloidosis
Interventions
Doxycycline
Lead sponsor
Medical College of Wisconsin
Results first posted
2020-01-07

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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