- Rosacea is a long-term facial skin condition. Its cause is not known and it cannot be cured, but treatment controls symptoms (NHS). Since 2017 the global ROSacea COnsensus (ROSCO) panels have classified it by phenotype rather than by the older subtypes (Tan et al. 2017).
- For the bumps and pustules, the best-tested topicals are topical ivermectin 1%, azelaic acid and metronidazole 0.75%. A 2016 network meta-analysis favoured ivermectin, but it was sponsored by its maker, Galderma (Siddiqui et al. 2016). A 2024 network meta-analysis, with no conflicts disclosed and a funding statement we did not see, ranked azelaic acid 20% highest and found ivermectin comparable to azelaic acid 15% and metronidazole (Shaheen et al. 2024).
- For persistent redness, brimonidine gel has the strongest trial base. Cochrane rated it high quality, though its US label notes that some trial patients had rebound redness (Cochrane 2015; Mirvaso label).
- Oral doxycycline at 40 mg is a sub-antimicrobial, anti-inflammatory dose. The US label says it should not be used for bacterial infections (Oracea label). Its main trial of 1,421 people was sponsored by its maker and was open-label (Galderma, 2010).
- Laser and intense pulsed light (IPL) help redness and small blood vessels in small trials. The best 2025 network meta-analysis was built on 25 randomised trials, mostly at unclear or high risk of bias, and two of its authors had received lecture fees from a device maker (Nguyen et al. 2025).
- Money trail: the main trials for ivermectin, brimonidine and doxycycline were run by, or for, Galderma, which sells all three. Galderma Group AG is listed on the Swiss exchange (SIX). L'Oréal holds a 20% stake, after private equity firm EQT fully exited in March 2026 (EQT, March 2026). Six of the twelve sources we graded are maker-funded or maker-run.
- Eye symptoms are not a topical-cream problem. Pain, blurred vision, light sensitivity or a red, gritty eye need same-day assessment, because they can signal keratitis (NHS).
Independent evidence review · Prescription medicine
Topical ivermectin, azelaic acid and metronidazole have the most independent trial support for the bumps and pustules of rosacea, and brimonidine has the best evidence for persistent redness. Most of the pivotal trials were run or paid for by the company that sells the drug, so our confidence is moderate for the creams and low to moderate for laser and light treatments. The newest independent network meta-analysis ranks the drugs differently from the older, maker-sponsored one, so no single "best" treatment is established. The evidence is strongest where independent reviews agree, and weakest where only a manufacturer has run a trial.
Table of contents
- Evidence summary
- What rosacea is, and how it is classified
- How the treatments are thought to work
- What works and what does not
- Benefits by claim
- Risks and all side effects
- Triggers, interactions and self-care
- Who should take extra care
- Doses studied and label doses
- Follow the money: who makes it and who funded the evidence
- Related research
- Frequently asked questions
- Sources and funding notes
Evidence summary
| Claim | Evidence | Source | Funding / conflict | Strength |
|---|---|---|---|---|
| Topical ivermectin 1% reduces inflammatory bumps and pustules | Two pooled pivotal trials and a 2016 network meta-analysis; Cochrane rated the evidence high quality, with two studies favouring ivermectin over placebo | Cochrane 2015; Siddiqui 2016 | Maker-sponsored trials and meta-analysis | Strong |
| Topical azelaic acid reduces bumps and pustules | Cochrane high-quality evidence; 2024 network meta-analysis ranked 20% gel highest | Cochrane 2015; Shaheen 2024 | Mostly company-run trials; the 2024 review disclosed no conflicts; its funding statement was not seen | Strong |
| Topical metronidazole 0.75% reduces bumps and pustules | Moderate-quality evidence in Cochrane; comparable effect to ivermectin in the 2024 network meta-analysis | Cochrane 2015; Shaheen 2024 | Mostly company-run trials | Moderate |
| Brimonidine gel reduces persistent redness for several hours | Cochrane high-quality evidence; pivotal trial reports show a benefit over vehicle; the duration and timing claims were not verified | Cochrane 2015; Fowler 2013 | Pivotal trials by Galderma R&D authors; funding statement not seen | Strong |
| Oral doxycycline 40 mg (sub-antimicrobial) reduces lesions | Cochrane found 100 mg better than placebo (high quality) and 40 mg about as effective with fewer side effects (grade not verified). The 40 mg community study was open-label with no comparator | Cochrane 2015; Galderma ORCA | ORCA sponsored by Galderma Laboratories | Moderate |
| Laser or IPL improves erythema and telangiectasia | Small trials, 4 studies and 141 people for IPL vs pulsed-dye laser; 25 RCTs with unclear or high risk of bias in the 2025 network meta-analysis | Zhai 2024; Nguyen 2025 | IPL meta funding not seen; society funding and device-maker lecture fees (2025 review) | Weak |
| Rosacea can be "phenotyped" without subtypes | Consensus panels by Delphi voting, 17 dermatologists and 3 ophthalmologists (2017), then 19 dermatologists and 2 ophthalmologists (2019) | Tan 2017; Schaller 2019/2020 | 2017 panel: grant record lists Galderma; 2019 funding statement not seen | Moderate |
| Skin burning and irritation with topical treatments | Ivermectin label: local burning and irritation (rates not checked); azelaic acid 15% had more adverse events than placebo in the 2024 review | Soolantra label; Shaheen 2024 | Labels are maker-written, FDA-reviewed | Risk |
| Rebound redness after brimonidine | Mirvaso label: some trial subjects had redness return worse than baseline, with no incidence given. Cochrane reports no rebound after stopping in the trials it covered | Mirvaso label; Cochrane 2015 | Label is maker-written | Risk |
Independent evidence and credibility scorecard
Independence tiers: Tier 1 (independent) = no identifiable financial stake in the result, such as public bodies and unfunded reviews; Tier 2 (indirect ties) = pooled evidence that relies on company-funded trials, or distant ties; Tier 3 (interested party) = a society, patient group or device-linked stake, not the direct seller; Tier 4 (self-interested) = produced, funded, sponsored or authored by the maker. Credibility runs from A (highest) to D (treat as advertising).
| Source | Who funds it | Country | Independence tier (1–4) | Credibility (A–D) | Why it would tell the truth / residual bias |
|---|---|---|---|---|---|
| NHS rosacea guidance | UK public funding through the NHS | UK | Tier 1 | A | A public health body accountable to patients and government, with no product to sell. Residual bias: a short patient summary that does not grade the evidence. |
| Cochrane, Interventions for rosacea (2015) | Funding of the review and its included trials not checked; the review covered 106 RCTs and 13,631 people | UK (London base; not separately verified) | Tier 2 | B | Systematic-review reputation depends on accuracy. Residual bias: the review can only be as independent as the company-funded trials it pools; its funding breakdown was not verified |
| Shaheen et al. 2024, JAAD International | No conflicts disclosed; funding statement not seen | Not verified (journal JAAD International) | Tier 1 | B | No conflicts disclosed, so Tier 1 is provisional until the funding statement is seen; a clear comparison of 19 trials. Residual bias: the trials it pooled were not checked one by one for funding, and several agents had few patients |
| Zhai et al. 2024, J Cosmet Dermatol | Funding and conflict statements not seen | Not verified (journal published by Wiley) | Tier 1 | B | No conflicts seen, but only 4 studies and 141 people. Residual bias: small sample and an unclear sign convention for some clearance results |
| Nguyen et al. 2025, JDDG | German Society for Dermatological Laser Medicine; two authors received lecture fees from Cynosure Lutronic, a device maker | Germany | Tier 3 | C | Society and device-linked ties in a field that sells machines. Residual bias: most of 25 trials at unclear or high risk of bias |
| Siddiqui et al. 2016, SpringerPlus | Sponsored by Galderma; two authors received research grants from Galderma; one author is a Galderma investigator | Not verified (journal SpringerPlus, Springer Nature) | Tier 4 | D | A maker-sponsored comparison of its own product. Residual bias: sponsor helped design the study, and the analysis is the sponsor's own comparison |
| Stein Gold et al. 2014, J Drugs Dermatol | Funding statement not visible on the page; authors list Galderma R&D affiliation | US-based authors (affiliations not fully verified) | Tier 4 | D | Company-run Phase III trials, with the maker's own staff on the author list. Residual bias: sponsor-run trial design and reporting |
| Fowler et al. 2013, J Drugs Dermatol (brimonidine) | Funding statement not visible on the page; two authors are Galderma R&D staff | US (affiliations include University of Louisville and Galderma R&D, Princeton NJ) | Tier 4 | D | Company-linked Phase III program. Residual bias: a later safety analysis of the same trials, seen only in search results, is reported to disclose Galderma employees and Galderma-supported manuscript work |
| Galderma, ORCA doxycycline community study | Sponsored by Galderma Laboratories L.P. | US | Tier 4 | D | Maker's own press release on its own community study. Residual bias: open-label, no comparator, and a sponsor headline |
| Tan et al. 2017, ROSCO panel, Br J Dermatol | Grant agency listed as Galderma (Europe PMC record); honoraria and voting-role statements not verified | UK journal; panel is international | Tier 4 | D | A sponsor-funded panel that moved clinicians to phenotype-based diagnosis. Residual bias: a sponsor-funded panel can shape which features are emphasised, even with blinded voting |
| Schaller et al. 2019/2020, ROSCO update, Br J Dermatol | Funding statement not seen; conflict statement is in an appendix we did not see | UK journal; panel is international | Tier 4 | D | Updated phenotype list with a 75% agreement threshold. Residual bias: same sponsor and paid-panel issues as the 2017 panel |
| National Rosacea Society | Donations from individuals and industry. Industry money funds awareness and education. The page names no companies. A 2017 post says it was sponsored by Galderma Laboratories | US | Tier 3 | C | Patient group with a mission to inform people with rosacea, and says health information is reviewed by independent physicians. Residual bias: a documented industry stake, including sponsored posts |
Convergence and clustering. The strongest signal is that the 2024 independent network meta-analysis, the Cochrane review and the NHS guidance all treat topical ivermectin, azelaic acid and metronidazole as first-line options for bumps and pustules. They disagree on the order, so no single winner is shown. Six of the twelve sources are maker-funded or maker-run, and a seventh, the National Rosacea Society, carries a Galderma-sponsored post. Our verdict therefore reflects a UK and US view, shaped by one company's products.
What this means: The independent evidence supports a real benefit for several topical creams on bumps and pustules, and for brimonidine on redness. The company-run trials that built the market are the weakest part of the record, and they make up most of the evidence for brimonidine and the 40 mg doxycycline dose. Where independent reviews reach the same conclusion, that conclusion is the safest one to rely on.
What rosacea is, and how it is classified
The NHS describes rosacea as a long-term skin condition that mainly affects the face. It is more common in women and in people with lighter skin, though symptoms can be worse in men. Early signs include flushing or warmth across the nose, cheeks, forehead, chin, neck and chest. Later signs can include constant redness, visible broken blood vessels, small pink or red bumps and, over many years, thickened skin mainly on the nose (NHS).
From subtypes to phenotypes
The older approach sorted patients into subtypes. The 2017 ROSCO panel recommended moving away from subtypes and classifying rosacea by the features a patient actually has. The panel judged two features diagnostic on their own: persistent centrofacial redness with periodic flares, which 17 of 17 panellists agreed on, and phymatous (thickened) skin changes, agreed by 13 of 17. Flushing, visible blood vessels and bumps were not diagnostic alone (Tan et al. 2017).
The 2019 update, by a panel of 19 dermatologists and 2 ophthalmologists, used at least 75% agreement. It grouped features into diagnostic (phymatous changes and persistent erythema), major (flushing or transient erythema, papules and pustules, telangiectasia) and minor (burning, stinging, dry sensation, oedema), plus ocular features such as lid-margin telangiectasia, blepharitis, keratitis, conjunctivitis and anterior uveitis (Schaller et al. 2019/2020). The 2017 panel's grant record lists Galderma, which sells rosacea products; the 2019 update's funding statement was not seen. Clinicians can use the classification, but the grading of which features matter most is a sponsor-funded opinion, not a neutral test.
The NHS page does not describe subtypes, and it lists look-alike conditions that should be considered, including acne, contact and seborrhoeic dermatitis, lupus and keratosis pilaris (NHS). A confident diagnosis, especially where eyes or thickened skin are involved, is a job for a GP or dermatologist.
How the treatments are thought to work
The cause of rosacea is not known. The NHS states it is not caused by poor hygiene and is not contagious (NHS). The leading treatments act on inflammation, on blood-vessel tone, or on the skin's microbes, and the mechanisms are only partly proven.
- Ivermectin 1% cream is licensed only for inflammatory lesions (papules and pustules), not for redness (Soolantra label). We did not verify a mechanism from a source we opened.
- Brimonidine gel is licensed for persistent redness, and the trials measured its effect over hours after each application (Mirvaso label; Fowler 2013). The reviews we opened do not describe its mechanism in detail.
- Doxycycline 40 mg is licensed as an anti-inflammatory dose. The label says plasma levels are below those needed to treat bacterial disease, and it warns that resistance may develop if the drug is misused (Oracea label).
- Lasers and IPL reduce visible redness and vessels in some patients in small trials. The 2025 review reports these effects but does not test a mechanism in detail (Nguyen 2025).
What works and what does not
| Treatment | Target | Evidence in one line | Verdict |
|---|---|---|---|
| Topical ivermectin 1% | Bumps and pustules | Cochrane high-quality evidence; slightly more effective than metronidazole in one study | WORKS |
| Topical azelaic acid 15% or 20% | Bumps and pustules | Cochrane high-quality evidence; highest ranked in the 2024 network meta-analysis, which also found more adverse events at 15% | WORKS |
| Topical metronidazole 0.75% | Bumps and pustules | Cochrane moderate-quality evidence; comparable to ivermectin in the 2024 network meta-analysis | WORKS |
| Brimonidine gel 0.33% (Mirvaso) | Persistent redness | Cochrane high-quality evidence; redness reduced in company-run trials (duration not verified) | WORKS |
| Oxymetazoline 1% cream (Rhofade) | Persistent redness | Approved by the FDA in 2017 for persistent facial redness; the pivotal trial reports were not available to us, so funding is unverified | MIXED |
| Oral doxycycline 40 mg (Oracea) | Bumps and pustules | Cochrane: 100 mg high-quality benefit over placebo; 40 mg about as effective with fewer side effects (grade not verified) | WORKS |
| Laser or pulsed-dye laser (PDL) | Telangiectasia and redness | Small trials; PDL with oxymetazoline ranked best for telangiectasia in the 2025 network meta-analysis, and radiofrequency microneedling beat PDL on satisfaction and erythema | MIXED |
| Intense pulsed light (IPL) | Redness and telangiectasia | Four trials, 141 people. IPL reached a higher share of patients with more than 75% clearance than PDL; no significant difference for erythema | MIXED |
| Trigger avoidance | Flares | Common triggers listed by the NHS; the strength of each trigger is not ranked | INSUFFICIENT |
Benefits by claim
Does ivermectin cream clear rosacea bumps?
Partly. Cochrane found topical ivermectin better than placebo in two studies (Cochrane 2015). In the 2016 network meta-analysis, which Galderma sponsored, ivermectin 1% beat metronidazole 0.75% with a risk ratio for treatment success of 1.17 (95% credible interval 1.08 to 1.29), and azelaic acid 15% twice daily with a risk ratio of 1.25 (1.14 to 1.37) (Siddiqui et al. 2016). One of its authors, Linda Stein Gold, is listed as a Galderma investigator. The later, unfunded 2024 network meta-analysis found ivermectin comparable to azelaic acid 15% and metronidazole, not clearly superior (Shaheen et al. 2024).
Does metronidazole work for bumps and pustules?
Yes, with moderate-quality evidence. Cochrane found topical metronidazole better than placebo for papulopustular rosacea, from three trials (Cochrane 2015). The 2024 network meta-analysis placed it in the same group as ivermectin and azelaic acid 15% (Shaheen et al. 2024). We did not check the funding of each metronidazole trial, so this rating is based on the review's own grading.
Does azelaic acid work?
Cochrane rates the benefit as high-quality, from four trials versus placebo (Cochrane 2015). The 2024 network meta-analysis gave azelaic acid 20% the highest ranking, with an odds ratio of 8.54 (95% CI 2.48 to 29.45) against placebo. The authors note the wide interval. The same review found azelaic acid 15% was the only topical agent with a significant increase in adverse events, odds ratio 1.95 (95% CI 1.30 to 2.93) (Shaheen et al. 2024).
Does brimonidine reduce redness?
Yes, for hours at a time. Cochrane rated brimonidine's effect on erythema as high quality, at three hours (Cochrane 2015). The two pivotal trials of 0.5% brimonidine tartrate gel, run by Galderma-linked authors, reported a benefit over vehicle; we could not verify the timing, day schedule or P values from the full report (Fowler et al. 2013). The FDA label describes the product for persistent, non-transient redness in adults 18 and over (Mirvaso label).
Does oxymetazoline (Rhofade) reduce redness?
The FDA approved oxymetazoline 1% cream in 2017 for persistent facial redness associated with rosacea (Aclaris press release, 2018). The company that acquired the rights, Aclaris Therapeutics, announced the deal closed on 30 November 2018, with the price not stated. We could not open the pivotal trial reports, so we cannot say how they were funded or how large the effect was. Treat the efficacy claim as unverified by independent work.
Does oral doxycycline help?
Yes, for bumps and pustules. Cochrane rated 100 mg doxycycline as better than placebo, with high-quality evidence. It found 40 mg about as effective as 100 mg, with fewer side effects; we could not verify the review's grade for that comparison (Cochrane 2015). The largest 40 mg study, ORCA, was sponsored by Galderma Laboratories. Of 1,421 patients in the intent-to-treat group, about 75% of the 826 monotherapy patients who completed the study were clear or near clear by week 12 (Galderma, 2010). The study had no comparator group, so it cannot show benefit over placebo.
Do lasers and IPL help redness and visible blood vessels?
There is some evidence, but it is weak. A 2024 meta-analysis of four studies with 141 people found IPL and pulsed-dye laser similar for erythema, and found a significantly higher share of patients with more than 75% clearance on IPL (Zhai et al. 2024). We could not see this study's funding or conflict statements. The sign convention for the clearance result is unclear in the paper, so we report the direction the authors state. The 2025 network meta-analysis of 25 RCTs found PDL with oxymetazoline was the top-ranked treatment for telangiectasia, with a mean difference of −0.58 (95% CI −1.03 to −0.14), while radiofrequency microneedling beat PDL on satisfaction and erythema (Nguyen et al. 2025). That review was supported by a German laser society and two authors had received lecture fees from a device maker.
Risks and all side effects
The most common side effects in the trials and labels are local. For ivermectin 1% cream, we did not check the label's side-effect rates line by line (Soolantra label). For brimonidine gel, the most common reactions on the US label are erythema, flushing and skin burning sensation (Mirvaso label). For oral doxycycline 40 mg, we did not check the label's reaction rates line by line (Oracea label).
Azelaic acid 15% was the only topical agent with a significantly higher rate of adverse events than placebo in the 2024 network meta-analysis (odds ratio 1.95, 95% CI 1.30 to 2.93), and the authors note that some agents had limited safety data (Shaheen et al. 2024).
Triggers, interactions and self-care
The NHS lists alcohol, spicy food, hot drinks, sunlight, hot or cold temperatures, aerobic exercise such as running and stress as common triggers. It advises daily SPF 30 sunscreen, gentle skincare, and avoiding heat and humidity where possible (NHS). The NHS does not rank how strongly each trigger drives flares, and we did not find a graded trigger study in our search, so we rate trigger avoidance as insufficiently tested.
We did not find independent interaction studies for these products in this search, and we did not verify interaction sections from the labels. Check any new medicine with a pharmacist, especially antibiotics and any medicine that makes skin more sensitive to sunlight. Because the NHS lists alcohol and spicy food as triggers, people who notice flares after drinking may want to note this and raise it with their clinician.
Who should take extra care
- Anyone with eye symptoms should be assessed urgently, as above (NHS).
- People taking oral antibiotics or with recurrent infections should discuss doxycycline with their clinician, because the Oracea label says the product is not for infections and warns of resistance (Oracea label).
- People with unexplained facial redness or thickened skin should see a dermatologist, because look-alike conditions include lupus and dermatitis (NHS).
- Pregnancy, breastfeeding and children: we did not verify label guidance on these groups for each product in this search. Ask a pharmacist or clinician before starting.
Doses studied and label doses
The doses below are the ones used in trials or stated on US labels. They are not personal instructions. Follow the prescriber's directions for any real treatment.
- Ivermectin 1% cream: label says once daily on affected areas of the face. The pivotal trials used 12 weeks of treatment, and some patients were treated for about a year (Soolantra label; Stein Gold 2014).
- Metronidazole 0.75% cream: twice daily in the 2016 and 2024 comparisons (Siddiqui 2016).
- Azelaic acid 15% gel: twice daily in the 2016 comparisons (Siddiqui 2016).
- Brimonidine 0.5% tartrate gel: once daily for 4 weeks, followed by 4 weeks of follow-up in the pivotal trials (Fowler 2013). The marketed product is a 0.33% gel, and the label gives its own directions (Mirvaso label).
- Doxycycline 40 mg modified-release (Oracea): one 40 mg capsule once daily in the morning, on an empty stomach, at least 1 hour before or 2 hours after meals (Oracea label).
Product quality. We did not find independent product-testing results for rosacea creams in this search. The Oracea label names Catalent Pharma Solutions as manufacturer; the country of that contractor was not verified.
Follow the money: who makes it and who funded the evidence
Who makes and sells the main products
- Galderma Laboratories, L.P. is the labeller for Soolantra (ivermectin 1% cream), Oracea (doxycycline 40 mg) and Mirvaso (brimonidine gel), and is based in Dallas, Texas, according to the DailyMed labels (Soolantra label; Oracea label; Mirvaso label).
- Galderma Group AG is the listed parent, traded on SIX. The company listed in 2024 (EQT, March 2026).
- Ownership. EQT, the private equity owner, fully exited Galderma Group AG on 13 March 2026, selling about 34.0 million shares for about CHF 4.9 billion in gross proceeds. An EQT fund affiliate received about CHF 1.3 billion. L'Oréal holds a 20% stake, built through two tranches after the listing (EQT, March 2026).
- Oxymetazoline (Rhofade). Allergan sold the worldwide rights to Aclaris Therapeutics, which closed on 30 November 2018. The price was not stated (Aclaris press release).
Who funded the trials and guidance
- Siddiqui et al. 2016: sponsored by Galderma, with research grants to two authors and Galderma investigator status for a third (Siddiqui 2016).
- ORCA doxycycline study: sponsored by Galderma Laboratories L.P. (Galderma 2010).
- ROSCO 2017 and 2019 panels: the 2017 grant record lists Galderma; honoraria not verified; the 2019 update's funding statement was not seen (Tan 2017; Schaller 2019/2020).
- Brimonidine pivotal trials: the report was on behalf of the Brimonidine Phase III Study Group, with two Galderma R&D authors (Fowler 2013). A later safety analysis of the same trials, seen only in search results and not opened, is reported to disclose Galderma employees and Galderma support for the manuscript.
- Ivermectin pivotal trials: published on behalf of the Ivermectin Phase III Study Group, with Galderma R&D affiliation. The visible page did not show a funding statement (Stein Gold 2014).
- Cochrane 2015: 106 included studies and 13,631 participants; we did not verify the review's funding breakdown (Cochrane 2015).
- Shaheen et al. 2024: no conflicts disclosed; funding statement not seen (Shaheen 2024).
- Laser review 2025: supported by the German Society for Dermatological Laser Medicine; two authors had lecture fees from Cynosure Lutronic (Nguyen 2025).
- National Rosacea Society: sustained by donations from individuals and industry. Industry money funds awareness and education, and the Society says it alone is responsible for those materials (NRS funding page). A May 2017 post states it was sponsored by Galderma Laboratories, L.P. (NRS 2017 post).
Documented integrity events
We did not find documented regulatory bans, warning letters, FTC actions or recalls for the rosacea products listed above in our search. We did not check the FDA warning-letter database or court records, so this is a gap rather than a finding of none.
Rosacea funding at a glance
12 sources graded. The counts below are the independence tiers assigned in the scorecard above. They count sources, not funding amounts or evidence quality.
Public funding alone does not prove independence, and commercial funding alone does not prove a claim false. Named funders, countries and relationships are in the scorecard and source notes.
Related research
Other skin-and-inflammation evidence reviewed by Pure City Research:
- Eczema prevention and management: evidence and safety guide
- Eczema supplements: evidence, uncertainty and safety
- Astaxanthin: skin, UV response, exercise and safety evidence
- Collagen: skin, joint and bone evidence, risks and funding
- Glutathione: skin trials, antioxidant markers and injection safety
- Melanoma: skin and nail symptoms, biopsy, staging and treatment
Frequently asked questions
Is rosacea still classified into subtypes?
The 2017 ROSCO panel recommended moving to a phenotype-based approach, and the 2019 update kept that model (Tan 2017; Schaller 2019/2020). The 2017 panel was funded by Galderma per its grant record, so the change is recommended by a panel with a documented sponsor.
Which cream works best for bumps?
No single cream has been shown to be best in independent work. Cochrane rates ivermectin, azelaic acid and metronidazole as effective (Cochrane 2015). The 2024 independent network meta-analysis ranked azelaic acid 20% highest and found ivermectin and metronidazole comparable to azelaic acid 15% (Shaheen 2024).
Does brimonidine gel cause redness to come back?
The Mirvaso label says some trial patients had redness return worse than their baseline, without an incidence rate (Mirvaso label). Cochrane reports no rebound after stopping in the trials it covered (Cochrane 2015). Discuss any worsening after stopping with a clinician.
Is the 40 mg doxycycline dose an antibiotic?
The Oracea label says the product is not for treating or preventing bacterial infections, and that plasma levels are below those needed to treat bacterial disease. It also warns that bacterial resistance may develop (Oracea label). The main trial was sponsored by the maker and open-label (Galderma 2010).
Do lasers or IPL cure rosacea?
No. They can reduce visible redness and small blood vessels in some people, but the evidence is weak. The 2024 IPL meta-analysis had 4 studies and 141 people (Zhai 2024). The 2025 network meta-analysis found most of its 25 trials at unclear or high risk of bias (Nguyen 2025).
Are the rosacea guidelines independent?
The 2017 ROSCO paper's grant record lists Galderma, and we could not verify honoraria or the 2019 update's funding (Tan 2017; Schaller 2019/2020). We could not open the British Association of Dermatologists guideline, so we cannot compare it on funding.
Who owns the company that makes Soolantra and Oracea?
Both are Galderma products labelled by Galderma Laboratories, L.P. (Soolantra label). The listed parent, Galderma Group AG, is traded on SIX. EQT fully exited in March 2026, and L'Oréal holds 20% (EQT, March 2026).
When should I see a doctor about rosacea?
The NHS advises a non-urgent GP appointment for rosacea symptoms, and a referral to a dermatologist if treatments are not working. Eye pain, blurred vision, light sensitivity or a red eye need an urgent GP appointment or a call to 111 (NHS).
Sources and funding notes
What we could not verify: the Cochrane risk ratios and funding breakdown (publisher full text blocked); the Shaheen and Zhai funding statements; the Tan honoraria and voting statements and the 2019 ROSCO funding; the adverse-event rates on the Soolantra, Mirvaso and Oracea labels; The funding statement for the 2014 ivermectin pivotal publication (Stein Gold et al.); the funding statements for the 2013 brimonidine trial report and the oxymetazoline pivotal trials; the Galderma-sponsored ORCA trial report itself (we used the company's press release); the Cochrane review's own funding and declarations of interest; the 2019 ROSCO conflict statement in its appendix; the British Association of Dermatologists 2021 guideline, which we could not open; the NICE brimonidine assessment (the page returned an error); the Oracea EMA referral (the PDF could not be read); the authors' countries for the 2016 ivermectin review, the 2024 azelaic-acid network meta-analysis and the 2024 IPL meta-analysis; and the location of Catalent Pharma Solutions. Two PubMed records (the 2017 and 2019 ROSCO papers) were rate-limited during this review, so we cite their DOI pages instead. The 2024 network meta-analysis reports 8,208 participants in its abstract and 8,075 in its results, so we avoid quoting a total. We found no independent trial of the creams on eye disease.
- NHS, Rosacea — UK public health guidance; funded by UK public funds.
- Van Zuuren EJ et al., Cochrane Interventions for rosacea, 2015 — systematic review of 106 RCTs (13,631 participants); funding breakdown not verified.
- Cochrane featured review, June 2015 — summary of the same review; no funding statement shown.
- Shaheen et al., network meta-analysis, JAAD International 2024 — 19 RCTs; no conflicts disclosed; funding statement not seen.
- Siddiqui K, Stein Gold L, Gill J, SpringerPlus 2016 — 19 RCTs; sponsored by Galderma; grants to two authors.
- Stein Gold L et al., J Drugs Dermatol 2014 — two pivotal ivermectin trials; funding statement not visible; Galderma R&D affiliation.
- Fowler J et al., J Drugs Dermatol 2013 — two pivotal brimonidine trials; Galderma R&D affiliation on two authors.
- Galderma, ORCA results press release, 2010 — maker's own release; sponsored by Galderma Laboratories L.P.
- Tan J et al., ROSCO panel, Br J Dermatol 2017 — grant record lists Galderma; honoraria not verified.
- Schaller M et al., ROSCO 2019 panel, Br J Dermatol (vol 182, 2020) — funded by Galderma; conflict statement in appendix not seen.
- Zhai Q et al., J Cosmet Dermatol 2024 — 4 studies, 141 participants; funding and conflict statements not seen.
- Nguyen L et al., J Dtsch Dermatol Ges 2025 — 25 RCTs; supported by the German Society for Dermatological Laser Medicine; lecture fees from Cynosure Lutronic for two authors.
- National Rosacea Society, How the NRS is funded — patient group; funded by individual and industry donations.
- National Rosacea Society, sponsored post, May 2017 — states sponsorship by Galderma Laboratories, L.P.
- Soolantra (ivermectin) cream label, DailyMed — labeller Galderma Laboratories, L.P., Dallas; maker-written, FDA-reviewed.
- Mirvaso (brimonidine) gel label, DailyMed — labeller Galderma Laboratories, L.P.; rebound statement; adverse reaction rates.
- Oracea (doxycycline 40 mg) label, DailyMed — labeller Galderma Laboratories, L.P.; dosing and antibacterial caveat.
- Aclaris Therapeutics press release, December 2018 — acquisition of Rhofade rights from Allergan; closed 30 November 2018; price not stated.
- EQT, Galderma Group AG full exit, 13 March 2026 — ownership change; L'Oréal 20% stake; SIX listing.
Educational research reviewed 9 October 2026. This article is not medical advice; talk to a qualified clinician or pharmacist before starting, stopping or combining treatments.
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