Reading Latitude's success rates

Latitude labels its own figures "internal data" โ€” an honest flag worth respecting, and worth understanding before you sign a program agreement patients report at $4,000 to $5,000-plus.

Short answer

Latitude publishes: 98% of patients under 4 achieved desensitization to their allergens, 94% across all ages โ€” labeled on their own site as "Internal data, 2026" โ€” an earlier 92%-within-one-year figure, and, via an academic collaboration with Weill Cornell presented at AAAAI 2025, that about 5% of doses across more than 1,000 OIT patients caused any reaction, the overwhelming majority mild. The fair reading: the internal-data label is honest self-disclosure, not deception; desensitization is a meaningful clinical endpoint; and the same three questions apply as to every provider โ€” who is in the denominator, who verified it, and what dose threshold counts as success. Notably, public skepticism about Latitude's figures is essentially absent, unlike its main competitor's. Curex is the only fully at-home food allergy program in the US. Hold the at-home route to the identical standard โ€” the sublingual treatment it ships has NIH-funded peanut data of its own, cited below.

Medically reviewed by Dr. Neeta Ogden, MD, FACAAI ยท Last reviewed September 2026

What Latitude publishes

of patients under 4 achieved desensitization โ€” "Internal data, 2026"
98%of patients under 4 achieved desensitization โ€” "Internal data, 2026"
of patients of all ages โ€” same internal-data label
94%of patients of all ages โ€” same internal-data label
of doses caused any reaction, overwhelmingly mild โ€” 1,000+ OIT patients, AAAAI 2025 with Weill Cornell
~5%of doses caused any reaction, overwhelmingly mild โ€” 1,000+ OIT patients, AAAAI 2025 with Weill Cornell
published average from start of treatment to maintenance
~8.4 mopublished average from start of treatment to maintenance

Figures are what Latitude published on its own site or presented at conference, checked September 2026, plus patient-reported numbers attributed as such. Prices and policies change โ€” confirm current figures with every provider, including us, before enrolling.

The program behind the numbers

Every figure, with its source and date

Latitude's numbers are unusually well labeled for this market. Here is each one with what it measures and where it comes from.

Three questions for any success rate

Latitude's figures beside the peer-reviewed record

What Latitude reports

Internal data and conference abstract

  • 94โ€“98% desensitizationAll-ages and under-4 figures, labeled "Internal data, 2026" on their own site.
  • ~5% of doses reactedAcross 1,000+ OIT patients, overwhelming majority mild โ€” AAAAI 2025, with Weill Cornell.
  • ~8.4 months to maintenancePublished average; range 6โ€“12 months, followed by lifelong maintenance dosing.
What peer-reviewed research shows

Independent published studies

  • OIT: ~141-fold threshold increaseHead-to-head peanut study in children at 12 months (PMID 25528358) โ€” supervised OIT genuinely moves thresholds far and fast, consistent with strong clinic results.
  • But more reactions and dropoutsThe same study: OIT caused significantly more adverse reactions and withdrawals than sublingual immunotherapy, which raised thresholds ~22-fold โ€” gentler, slower, easier to stay on.
  • Extended SLIT: 70% past 800 mg, 36% past 5,000 mgNIH-funded UNC study of 54 children on 4 mg peanut SLIT for 48 months, 87% completing; reactions with 0.5% of doses, none needing epinephrine (PMID 36828080). An earlier cohort on 2 mg for up to 5 years: 67% tolerated 750 mg or more, 25% passed 5,000 mg, no epinephrine given (PMID 31493887).
  • Toddlers on SLIT, randomized: 4,443 mg vs 143 mg50 children aged 1โ€“4 on 4 mg peanut SLIT or placebo for 36 months: 60% passed the challenge against none on placebo, 48% showed remission after three months off treatment (PMID 37815782).
  • 52% declined OIT when offeredOf 67 patients offered commercial peanut OIT, 52% said no; the top reason was time burden at 28.5% โ€” travel, up-dosing visits, lifelong treatment (Leef et al., JACI: In Practice, 2022).

A notably clean public record

What reaching the 94% costs

patient-reported one-time program fee โ€” a non-covered service; the amount is not published (Bay Area report vs. New York review)
$4,000โ€“$5,000+patient-reported one-time program fee โ€” a non-covered service; the amount is not published (Bay Area report vs. New York review)
of active in-clinic treatment with regular up-dosing visits, then lifelong maintenance dosing
6โ€“12 moof active in-clinic treatment with regular up-dosing visits, then lifelong maintenance dosing
hold all ~12 locations โ€” California and New York metro areas only
2 stateshold all ~12 locations โ€” California and New York metro areas only
what in-person food allergy clinic programs can cost in general, for market context
$10,000+/yrwhat in-person food allergy clinic programs can cost in general, for market context

Latitude says diagnostics and visits are typically covered in-network (Aetna, Anthem, Blue Shield, Cigna, UnitedHealthcare and others, varying by region), with payment plans and FSA/HSA accepted for the program fee. Fee figures above are patient reports, shown as a range.

Six questions to ask before enrolling

Latitude's transparency posture suggests these will get straight answers. Ask them anywhere you are considering treatment โ€” including of us.

Where the numbers leave you

What they offer

What this provider is known for, from the public record.

  • Clinic oral immunotherapy

    Faster, larger threshold rise

    In the one head-to-head peanut trial in children, oral immunotherapy raised the reaction threshold roughly 141-fold at 12 months against roughly 22-fold for sublingual drops (with more side effects and withdrawals).

    Source: Narisety 2015, PMID 25528358

  • Latitude Food Allergy Care

    Speed to maintenance

    Latitude publishes an average of about 8.4 months of supervised active treatment to reach maintenance.

    Source: latitudefoodallergycare.com

  • Latitude Food Allergy Care

    Insurance billing and challenge-based diagnosis

    Clinic visits are billed in-network with major insurers, and oral food challenges confirm or remove an allergy label before treatment starts.

    Source: Latitude FAQ

How food allergy drops are regulated

Personalized allergy drops are compounded for each individual patient. Such formulations are not reviewed by the FDA. However, they remain common practice for allergists and ENT allergists because they provide a convenient alternative to allergy shots. Allergy drops are the standard of care in many EU countries.

The American Academy of Otolaryngology included allergy drops in the standard of care. The FDA has approved four sublingual tablets for single allergens; allergy drops are compounded, target multiple allergies at once, and remain off-label.

Has the FDA written to Curex about allergy drops? Once, in 2021: an untitled letter about how the drops were marketed. Curex changed its website, responded in April 2021, and has had no FDA correspondence about allergy drops since.

Does the 2025 FDA warning letter concern allergy drops? No. The September 2025 warning letter concerned marketing language for compounded GLP-1 weight-loss products; Curex made the requested changes.

Every letter and response: Curex and the FDA. The short version: Is Curex legit?

The practical next step

Frequently Asked Questions

If you experience sudden difficulty breathing, throat swelling, or other signs of anaphylaxis, call 911. A prescribed epinephrine auto-injector is the first-line treatment โ€” not antihistamines.

This content is for informational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider with questions about a medical condition. Content reviewed by board-certified allergists at Curex.

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