CHAMGAP
APPROVEDReviewed and approved by the Chamgap Editorial Team (2026-08-15). The draft was written by AI, the existence of all 1 cited sources was verified at the original page, and the verdict passed blind grading and adversarial audit. Methodology v0.7.
Verdict No. 2693 · Search date 2026-08-15 · Methodology v0.7

Long-term add-on azithromycin,
does it really help with Reduced moderate and severe asthma exacerbations over 48 weeks?

30-Second Summary
B
Evidence Grade B · 76 · Safety caution
Long-term add-on azithromycin reduced asthma exacerbations in adults uncontrolled on inhaled maintenance therapy
Diarrhea was more common, and QT prolongation, hearing effects, drug interactions, and antimicrobial resistance require specialist screening and monitoring.
What the
research shows
The grade is B with 76 points. In 420 AMAZES participants, exacerbation rates were 1.07 versus 1.86 per person-year, IRR 0.59 (95% CI 0.47 to 0.74).
What the
ads claim
Benefit was shown under specialist conditions after QT and hearing screening while background inhaled therapy continued for 48 weeks.
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Useful facts when choosing a product

  • The tested regimen was azithromycin 500 mg three times weekly for 48 weeks.
  • People with hearing impairment or abnormal QTc prolongation were excluded.
  • The registration is ACTRN12609000197235.
Gap Measurement · Verdict 2693 · B 76
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

The paper reports central concealed allocation from a computer-generated table with permuted blocks of 4 or 6, placebo masking of participants and investigators, and agreement between registered and published coprimary outcomes. The exacerbation-rate primary outcome included all 420 participants in their assigned groups, but the paper did not report how missing 48-week AQLQ data for the coprimary quality-of-life outcome were handled. Follow-up lasted 48 weeks and both coprimary outcomes succeeded. The Australian NHMRC and John Hunter Hospital Charitable Trust funded the trial. Author pharmaceutical relationships were disclosed separately from trial funding.

02

Why this is classified as B (76)

A large publicly funded double-blind trial succeeded on both coprimary outcomes, but handling of missing 48-week AQLQ data was not reported and one confirmatory trial gives B with 76 points.

Counterpoint. Resistance, QT prolongation, hearing effects, gastrointestinal adverse events, and interactions require specialist selection and monitoring.

Rejudgment record. Cross-check applied — The Lancet paper and ACTRN12609000197235 establish both coprimary outcomes, central concealed allocation, participant and investigator masking, assigned-group analysis for exacerbations, unreported AQLQ missing-data handling, 48-week follow-up, and public-charitable funding

Scoring profile behind this grade
EndpointHHard endpoint - actual events such as death
ReplicationR1Single confirmatory trial
IndependenceI2Decisive evidence is publicly or non-profit funded
Effect sizeE+Meets the clinically important threshold

The scoring table and the verdict agree (B).

Sub-claim grades by effect

This ingredient is marketed for several effects. A single overall grade blends strong and weak claims together, so each effect is graded separately here. The overall grade reflects the strongest disconfirming or core claim.

Effect (sub-claim)GradeBasis
Reduced moderate and severe asthma exacerbationsBThe IRR was 0.59 (0.47 to 0.74).

Cross-check — Codex and Claude

This verdict was drafted by Codex through literature review and source-existence checks, cross-checked through blind grading and adversarial audit, and settled by reapplying the methodology boundary rules. Cases with split grades were resolved through rejudgment.
03

Evidence Table

StudyDesignSampleFundingEndpointResultWeight
Gibson PG, Yang IA, Upham JW, Reynolds PN, Hodge S, James AL, Jenkins C, Peters MJ, Marks GB, Baraket M, Powell H, Taylor SL, Leong LEX, Rogers GB, Simpson JL. 2017Multicenter double-blind placebo-controlled randomized trial207Australian NHMRC and John Hunter Hospital Charitable TrustCoprimary 48-week moderate/severe exacerbation rate and AQLQExacerbation rates 1.07 versus 1.86 per person-year; IRR 0.59 (95% CI 0.47 to 0.74), P<.0001; AQLQ difference 0.36 (0.21 to 0.52)Pivotal single independently funded confirmatory trial
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Receipt — 1 References

All 1 cited sources were verified for existence at the original page (as of 2026-08-15).

Gibson PG, Yang IA, Upham JW, Reynolds PN, Hodge S, James AL, Jenkins C, Peters MJ, Marks GB, Baraket M, Powell H, Taylor SL, Leong LEX, Rogers GB, Simpson JL. Effect of azithromycin on asthma exacerbations and quality of life in adults with persistent uncontrolled asthma (AMAZES). Lancet. 2017;390(10095):659-668. PMID: 28687413. DOI: 10.1016/S0140-6736(17)31281-3. ACTRN12609000197235.
checked
Draft and rewrite: Codex (AI) · Verification: Codex blind grading and adversarial audit · Final adjudication: Claude
Reviewed and approved: Chamgap Editorial Team · Approval date: 2026-08-15 · Corrections: none

Cite this verdict

Long-term add-on azithromycin x fewer exacerbations in uncontrolled asthma Evidence Grade B card
[Chamgap] Long-term add-on azithromycin x fewer exacerbations in uncontrolled asthma — Evidence Grade B·76. 1 cited sources checked. Source: https://chamgap.com/en/verdicts/immunity/long-term-azithromycin-uncontrolled-asthma-exacerbations/ · CC BY 4.0

CC BY 4.0 — free to use with attribution; do not distort grades, numbers, or verdict meaning.

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What this document does and does not do

Chamgap is an information source. It reports what research has and has not confirmed; it does not tell readers what to take or buy. That decision belongs to readers and, when needed, medical or legal professionals. This verdict reflects literature available up to the search date and may change as new research appears. Nothing here is medical advice.