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Letybo®’s U.S. Launch: A Provider’s Guide to the Newest Neurotoxin

The neurotoxin market is more crowded than ever. With six FDA‑approved options now available, you might be wondering: do I really need to add another product to my practice? 

The recent U.S. launch of Letybo® (letibotulinumtoxinA‑wlbg), South Korea’s #1 neurotoxin, is making that a critical question for aesthetic providers. 

But beyond its fast onset and competitive price, its clinical data reveals a compelling safety feature that could address long‑term patient outcomes. 

This article will break down what you need to know about Letybo and how it stacks up against the competition, helping you decide if it’s the right fit for your practice and your patients.

What you will learn in this article:

  • How Letybo® stacks up against Botox® and Daxxify®—the established gold standard and the other new competitor—in terms of onset, duration, and cost. 
  • The unique clinical characteristics of Letybo®, including its formulation and diffusion pattern. 
  • Strategic insights on whether to incorporate Letybo® into your practice, based on early provider experiences. 
  • Actionable tips for communicating with patients about this new treatment option.

Table of Contents

Letybo: The “K‑Beauty Botox” Arrives in the U.S.

While new to the U.S., Letybo® has a long track record of success internationally, where it is known as Botulax and other brand names. With over 31 million treatments administered globally across more than 65 countries, it’s a major player in the international aesthetics market. 

Its FDA approval in February 2024 for the treatment of moderate to severe glabellar lines in adults was based on three Phase III trials involving more than 1,000 participants, which demonstrated its safety and efficacy. 

For a detailed overview of Letybo’s FDA approval and clinical trial data, you can read the IAPAM’s initial coverage: Letybo®: A New FDA‑Approved Neurotoxin for Glabellar Lines.

Letybo vs. Botox vs. Daxxify: A Head‑to‑Head Comparison

Let’s break down how Letybo® compares to Botox® and the other new kid on the block, Daxxify®. 

Understanding these newer products helps you make strategic decisions about your neurotoxin portfolio. 

For a comprehensive comparison of all six FDA‑approved neurotoxins, see our complete neurotoxin comparison guide.

Feature Letybo® Botox® Daxxify®
Onset 2–7 days (often visible by day 3–5) 3–7 days 3–7 days
Duration 3–4 months 3–4 months 6–9 months
Formulation LetibotulinumtoxinA (type A, high purity) OnabotulinumtoxinA DaxibotulinumtoxinA with peptide carrier
Diffusion Similar to other toxins (moderate) Moderate Low–moderate (precision‑focused)
Patient Cost* ≈ $9–$13 per unit ≈ $10–$18 per unit Higher per treatment than Botox
Best For Faster onset, natural look, cost‑conscious patients Gold standard, broad applications Longest duration, fewer annual visits

*Typical U.S. practice pricing; actual fees vary by clinic and market.

Letybo®

  • Onset: 2–7 days, often visible by day 3–5
  • Duration: About 3–4 months
  • Formulation: LetibotulinumtoxinA (type A, high‑purity)
  • Diffusion: Similar to other toxins (moderate), designed for precise placement
  • Typical patient cost: Around $9–$13 per unit in many U.S. practices*
  • Best for: Patients who want faster onset, a soft, natural look, and a slightly lower price point

Botox®

  • Onset: Typically 3–7 days
  • Duration: About 3–4 months
  • Formulation: OnabotulinumtoxinA
  • Diffusion: Moderate, with a long track record and predictable results
  • Typical patient cost: Around $10–$18 per unit, depending on market* 
  • Best for: Patients who prefer the long‑standing “gold standard” with broad on‑ and off‑label uses

Daxxify®

  • Onset: Usually within 3–7 days
  • Duration: About 6–9 months for most patients
  • Formulation: DaxibotulinumtoxinA with a proprietary peptide carrier
  • Diffusion: Low–moderate, often chosen for high precision
  • Typical patient cost: Higher per treatment than Botox, though fewer sessions per year
  • Best for: Patients who prioritize longest duration and fewer visits, and are comfortable with a higher upfront cost

*Typical U.S. practice pricing ranges; actual fees vary by clinic and region.

What Makes Letybo® Different?

Beyond the comparison chart, Letybo® has several unique characteristics that are generating buzz among providers.

  • Faster Onset: In clinical studies, patients often noticed improvement within about 2–3 days, with some reporting changes as early as Day 1. 
  • Exceptional Immunogenicity Profile: In the pivotal BLESS Phase 3 trials, which included more than 1,200 subjects, no neutralizing antibodies were detected, even after repeat treatments. This suggests a very low risk of treatment‑induced resistance in the studied population, a critical factor for long‑term patient care. 
  • Precise Diffusion: Many providers report that Letybo® has a controlled, predictable spread, which can make it appealing for precision work in areas like the glabellar complex. 
  • The “K‑Beauty” Appeal: Originating from South Korea, where letibotulinumtoxinA is widely used and often framed as a top Korean neurotoxin, Letybo® taps into the strong global interest in K‑Beauty and can be a compelling marketing story for patients seeking the latest aesthetic innovations.

“As a physician, I welcome the introduction of newer toxins with newer manufacturing processes that can deliver a highly purified product with an excellent safety profile,” Ava Shamban, MD, a board‑certified dermatologist and clinical investigator on the FDA trials for Letybo told Allure Magazine.

Common Treatment Areas and Dosing Considerations

While Letybo® is FDA‑approved for treating moderate to severe glabellar lines (the “11s”), experienced providers are also using it for common off‑label applications. 

Dosing should always be tailored to the individual, but here are some typical starting points for discussion, based on the pivotal trials and common practice patterns:

  • Glabellar Lines: 20 units is the standard FDA‑approved dose
  • Forehead Lines: 10–20 units are often used for horizontal forehead lines
  • Crow’s Feet: 10–12 units per side is a common starting point for lateral canthal line
It is critical to remember that while dosing may seem similar to other neurotoxins, Letybo units are not directly interchangeable, and injection techniques may require adjustment.

Ideal Patients for Letybo®

Taken together, these qualities make Letybo® a strong option for patients who want a softer, natural aesthetic, faster visible results, and better value, especially those who are newer to injectables or excited by K‑Beauty–inspired treatments.

  • Patients seeking natural‑looking results: Many practices highlight Letybo’s “soft, natural finish” and “ultra‑smooth, natural results,” with less risk of a stereotypical “frozen” look, which appeals to patients who want to look refreshed rather than overdone. 
  • Cost‑conscious patients who still prioritize quality: Clinics frequently price Letybo® about 10–20% below Botox® per treatment while reporting comparable clinical outcomes, making it attractive for patients who want high‑quality results at a more accessible price point. 
  • Patients who value faster onset: Many providers note that Letybo often begins working within about 2–3 days, with some patients seeing changes as early as day 1–2, which is appealing for those seeking quicker visible improvement before events or photos. 
  • Neurotoxin‑naïve or “toxin‑curious” patients: Several practices report that first‑time neurotoxin users gravitate to Letybo® because it’s perceived as a gentler introduction, with subtle, natural results and a less intimidating “feel” than more established brands. 
  • Patients drawn to K‑Beauty and Korean aesthetics: As a Korean‑developed neurotoxin frequently marketed as part of the K‑Beauty movement, Letybo® resonates with patients who follow Korean skincare and aesthetic trends and want to try “the latest K‑Beauty injectable.”

What to Expect: The Letybo® Treatment Journey

For providers setting patient expectations, the Letybo® treatment process is straightforward and similar to other neurotoxin treatments. Here is a concise overview you can share with patients:

  • The Consultation: The first step is always a thorough consultation to discuss aesthetic goals, assess muscle movement, and determine if Letybo is the right choice. 
  • The Treatment: The injection process itself is quick, typically lasting only 5–10 minutes. A fine needle is used to administer the product with minimal discomfort. 
  • The Results: Patients can expect to see initial results within 2–3 days, with the full effect visible at around 1–2 weeks. 
  • The Aftercare: Post‑treatment care is simple: avoid strenuous exercise, excessive heat, and rubbing the treated area for the first 24 hours to ensure the product settles correctly.
For a more detailed guide you can provide to your patients, stay tuned for our comprehensive patient‑facing article on the Letybo experience.

Strategic Considerations for Your Practice

The decision to add a new neurotoxin to your practice is a strategic one. Here are some key factors to consider.

The Provider Perspective

Early provider experiences with Letybo® highlight the importance of technique adaptation. 

According to published reports and clinical commentary, while Letybo® shares similarities with Botox®, injectors note that dosing strategies and injection patterns may require adjustment to achieve optimal results. 

Provider training materials emphasize that Letybo units are not interchangeable with Botox®, and practitioners report that understanding these differences is key to patient satisfaction.

The Business Case

From a business perspective, Letybo®’s lower price point—often estimated at roughly 10–25% less than Botox® per unit in many U.S. practices—can be a compelling advantage. 

This may allow you to offer more competitive pricing to cost‑conscious patients without compromising on treatment quality, as long as you invest in patient education and marketing to build awareness for a newer brand.

Patient Communication

When introducing a new product, patient communication is key. Here are some tips for talking to your patients about Letybo®:

  • Leverage the K‑Beauty Connection: For patients familiar with K‑Beauty, highlighting Letybo®’s status as a leading Korean neurotoxin can be a powerful endorsement. 
  • Focus on the Benefits: Emphasize the faster onset and natural‑looking results that many patients desire. 
  • Offer it as an Option: Instead of positioning Letybo® as a replacement for Botox®, present it as another excellent option in your toolkit, allowing you to customize treatments to each patient’s unique needs and goals.

For more guidance on navigating the various neurotoxin options with your patients, refer to the IAPAM’s comprehensive guide: Neurotoxins in your Aesthetic Practice.

Key Takeaways

  • Letybo® is a new FDA‑approved neurotoxin with a faster onset and a price point that is competitive with Botox®. 
  • It has a strong international track record and is widely used in South Korea and other markets. 
  • While similar to other neurotoxins, it may require adjustments in injection technique to achieve optimal results. 
  • Adding Letybo® to your practice can provide a competitive advantage and a cost‑effective treatment option for your patients.

Conclusion

Letybo®’s arrival in the U.S. market represents an important addition to the neurotoxin landscape, offering providers a clinically validated option with a faster onset, competitive pricing, and an exceptional immunogenicity profile. 

While it shares many similarities with established products like Botox®, its unique characteristics—particularly the zero neutralizing antibody rate in clinical trials and its K-Beauty appeal—make it a strategic choice for specific patient populations. 

Whether Letybo® becomes a cornerstone of your practice or a complementary option alongside Botox® and other neurotoxins will depend on your patient demographics, practice positioning, and willingness to invest in provider training and patient education. 

For practices looking to differentiate themselves with cost-effective, natural-looking results and faster patient satisfaction, Letybo® deserves serious consideration.

FAQs

Is Letybo® as safe as Botox®?

Yes, Letybo® underwent rigorous clinical trials to receive FDA approval and has been used safely in millions of treatments worldwide.

Are the units for Letybo® and Botox® interchangeable?

While the dosing is similar, it is crucial to follow the manufacturer’s guidelines for reconstitution and dosing. As many experienced providers note, injection techniques may need to be adjusted for optimal results.

What are the common side effects of Letybo®?

Like other neurotoxins, the most common side effects are temporary and mild, including bruising, swelling, redness at the injection site, and headache. These typically resolve within a few days.

What should I avoid after a Letybo® treatment?

To ensure the best results, patients should avoid strenuous exercise, saunas, and excessive alcohol for 24 hours. It’s also recommended to avoid lying down for at least 4 hours post‑treatment.

How does Letybo® compare to Dysport® or Xeomin®?

Letybo®’s profile is often compared to Botox®. Dysport® is known for having a wider diffusion, which can be beneficial for larger areas like the forehead, while Xeomin® is a “naked” neurotoxin without complexing proteins. For a full breakdown, see our complete neurotoxin comparison guide.

How does Letybo®’s cost compare to other neurotoxins?

Letybo® is generally priced lower than Botox, making it a cost‑effective option for both providers and patients.

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References:

  1. BENEV / Hugel – “BENEV Company, Inc. and Hugel Inc. are pleased to announce that Letybo® (letibotulinumtoxinA‑wlbg) is now fully commercialized in the U.S., marking a significant milestone in the neuromodulator market” – 2025‑03‑25
  2. U.S. Food and Drug Administration – “Drug Trials Snapshots: LETYBO” – 2024‑03‑21 
  3. The Aesthetic Society / Oxford University Press – “Efficacy and Safety of Letibotulinumtoxin A in the Treatment of Glabellar Lines: A Randomized, Double‑Blind, Multicenter, Placebo‑Controlled Phase 3 Study” – 2022‑05‑17
  4. Swissmedic – “Swiss Public Assessment Report – Letybo 50 units powder for solution for injection” – 2023‑12‑06 
  5. HPRA (Ireland) – “Letybo 50 units powder for solution for injection – Summary of Product Characteristics” – 2023‑07‑11 
  6. FDA / CDER – “Drug Trials Snapshots – 2024 (includes LETYBO listing)” – 2024‑12‑30
  7. Dermatology Education Foundation – “Letybo from Hugel is the Newest Botulinum Toxin Approved in US” – 2024 
  8. Oxford University Press (ASJ Open Forum) – “Efficacy and Safety of LetibotulinumtoxinA in the Treatment of Vertical Glabellar Lines: Post Hoc Analyses of Phase 3 Clinical Study Data” – 2024‑01‑03 
  9. Letybo USA – “Letybo HCP” – 2025‑02‑12
  10. Express Med Spa – “Letybo Price 2025: Is It Cheaper Than Botox?” – 2025‑08‑21
  11. Express Med Spa – “Letybo vs Botox: What’s the Difference and Which Is Right for You?” – 2026‑01‑23
  12. Belorens – “Daxxify vs Botox: Differences, Results, Cost & Side Effects” – 2025‑09‑27
  13. Vogue – “The ‘K‑Beauty Botox’ is Here: Everything You Need to Know” – 2025‑10‑13
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