CHAMGAP
APPROVEDReviewed and approved by the Chamgap Editorial Team (2026-07-13). The draft was written by AI, the existence of all 3 cited sources was verified at the original page, and the verdict passed blind grading and adversarial audit. Methodology v0.6.
Verdict No. 247 · Search date 2026-07-13 · Methodology v0.6

Andrographis,
does it really help with Reduction of common-cold symptoms and duration?

30-Second Summary
B
Evidence Grade B · 60 · Safety caution
There are signals of improvement in common-cold symptoms and time to resolution, but formulation heterogeneity and study-quality limitations are substantial
What the
research shows
An independent meta-analysis of 33 RCTs and 7,175 participants found symptom-relief signals for cough at SMD -0.39 and sore throat at SMD -1.13, supporting B for relief. However, only four trials were placebo comparisons, 73% were unblinded, and combination products such as Kan Jang were included. Duration is C because I² was 96% to 98% and a manufacturer-sponsored 300-person trial was positive only on day 3. The overall grade is B with 60 points.
What the
ads claim
Marketed products use expressions such as 'immune support,' 'natural antiviral,' 'cold prevention,' and 'faster recovery.' The research scope is symptom scores and time to resolution over several days after a cold begins, which is distinct from evidence for preventing infection, clearing viruses, or preventing severe complications.
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Useful facts when choosing a product

  • Clinical trials include both single extracts standardized to andrographolides and fixed combinations containing Eleutherococcus.
  • The 2023 single-extract trial used AP-Bio 200 mg/day and 400 mg/day for 7 days.
  • Main outcomes included WURSS-21, cough, sore throat, overall symptom scores, and time to symptom resolution.
  • Gastrointestinal symptoms and skin reactions were the main nonserious adverse events reported with oral preparations.
Gap Measurement · Verdict 247 · B 60
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

The independent Hu 2017 systematic review included 33 RCTs with 7,175 participants and reported cough at SMD -0.39 and sore throat at SMD -1.13. However, only four studies were placebo comparisons, 73% were unblinded, and combination products such as Kan Jang were included. Heterogeneity for symptom duration was I² 96% to 98%. The manufacturer-sponsored Raj 2023 RCT of 300 participants found a WURSS-21 difference only on day 3, with no difference on days 5 and 7.

02

Why this is classified as B (60)

Symptom relief is B on the independent cough and sore-throat meta-analysis, limited by only four placebo comparisons, 73% unblinded trials, and inclusion of combinations such as Kan Jang. Duration is C because I² was 96% to 98% and the manufacturer-sponsored 300-person trial was positive only on day 3. The overall result is B with 60 points.

Counterpoint. A short-term early symptom-relief signal, particularly for cough and sore throat, remains across several studies. This judgment does not generalize results from specific extracts to every andrographis product or to infection prevention.

Rejudgment record. Reassessment (cross-check reflected) — Symptom relief is B based on an independent meta-analysis of 33 RCTs and 7,175 participants, limited by four placebo comparisons, 73% unblinded trials, and combination products; duration is C because I² was 96% to 98% and the manufacturer-sponsored 300-person trial was positive only on day 3

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
Relief of common-cold symptomsBAn independent meta-analysis and several RCTs show signals of improvement in cough, sore throat, and overall symptoms, but study quality and formulation heterogeneity are substantial.
Shortening symptom durationCDuration analyses had I² of 96% to 98%, and the manufacturer-sponsored 300-person trial differed only on day 3.

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
Hu XY et al. 2017Independent systematic review and meta-analysis7,175Independent UK NIHR SPCR fundingCough, sore throat, overall symptoms, time to symptom resolution, and adverse eventsSignals of improved cough and sore throat and shorter time to resolution versus placebo; overall methodological quality of included trials was poor.Key
Melchior J et al. 2000Randomized double-blind placebo-controlled pilot and phase III trials179Unknown; commercial fixed-combination productPatient symptom scores and physician diagnostic scoresImproved total symptom and diagnostic scores in the phase III trial; evidence came from an andrographis-Eleutherococcus fixed combination.Supportive
Raj JP et al. 2023Phase III double-blind randomized placebo-controlled trial300Sponsored by Natural Remedies Private LimitedWURSS-21, nasal mucus weight, mucociliary clearance, and IL-8WURSS-21 was positive on day 3 but showed no between-group difference on days 5 and 7, and objective measures were not significant.Key
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Receipt — 3 References

All 3 cited sources were verified for existence at the original page (as of 2026-07-13).

Hu XY, Wu RH, Logue M, Blondel C, Lai LYW, Stuart B, Flower A, Fei YT, Moore M, Shepherd J, Liu JP, Lewith G. Andrographis paniculata (Chuān Xīn Lián) for symptomatic relief of acute respiratory tract infections in adults and children: A systematic review and meta-analysis. PLoS One. 2017;12(8):e0181780. PMID: 28783743. DOI: 10.1371/journal.pone.0181780.
checked
Melchior J, Spasov AA, Ostrovskij OV, Bulanov AE, Wikman G. Double-blind, placebo-controlled pilot and phase III study of activity of standardized Andrographis paniculata Herba Nees extract fixed combination (Kan jang) in the treatment of uncomplicated upper-respiratory tract infection. Phytomedicine. 2000;7(5):341-350. PMID: 11081985. DOI: 10.1016/S0944-7113(00)80053-7.
checked
Raj JP, Maurya MR, Nair N, Marfatia H, Hadaye R, Gogtay NJ. Efficacy and safety of AP-Bio®(KalmCold®) in participants with uncomplicated upper respiratory tract viral infection (common cold) - A phase III, double-blind, parallel group, randomized placebo-controlled trial. Complement Ther Med. 2023;73:102934. PMID: 36842634. DOI: 10.1016/j.ctim.2023.102934.
checked
Draft and rewrite: Codex (AI) · Verification: Codex blind grading and adversarial audit · Final adjudication: Claude
Reviewed and approved: Chamgap Editorial Team · Approval date: 2026-07-13 · Corrections: none

Cite this verdict

Andrographis (Andrographis paniculata) x reduction of common-cold symptoms and duration Evidence Grade B card
[Chamgap] Andrographis (Andrographis paniculata) x reduction of common-cold symptoms and duration — Evidence Grade B·60. 3 cited sources checked. Source: https://health-receipt.pages.dev/en/verdicts/immunity/andrographis-common-cold-symptoms-duration/ · 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.