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Understanding: What is the generic for cantharidin?

3 min read

First approved by the FDA in 2023, Ycanth (cantharidin) is a brand-name prescription medication, and there is currently no generic product available in the United States. This means that while cantharidin is the active ingredient, patients cannot obtain a therapeutically equivalent, generic version on the U.S. market.

Quick Summary

The generic name for the active ingredient in the brand-name drug Ycanth is cantharidin. There is currently no generic version of Ycanth available in the U.S.

Key Points

  • Generic vs. Brand Name: Cantharidin is the generic name for the active ingredient, while Ycanth is the brand name of the first FDA-approved product.

  • No Generic Product Available: As of now, there is no therapeutically equivalent generic product of Ycanth available in the United States.

  • Used for Molluscum Contagiosum: Ycanth was approved in 2023 for the topical treatment of molluscum contagiosum in patients aged 2 and older.

  • Vesicant Action: Cantharidin works by causing the skin to blister, which helps to separate and remove the affected lesions from healthy skin.

  • Administered by a Healthcare Provider: Due to safety risks, cantharidin must be applied by a medical professional in a clinical setting.

  • Compounding History: Prior to Ycanth's approval, cantharidin was available through compounding pharmacies for treating warts and molluscum.

  • Risk of Oral Toxicity: Cantharidin is highly toxic if ingested and must be used with extreme caution to prevent accidental swallowing.

In This Article

What is Cantharidin?

Cantharidin is a colorless, odorless fatty substance derived from beetles belonging to the family Meloidae, commonly known as blister beetles. Historically, it was a component of folk remedies and was notoriously used as an aphrodisiac under the name "Spanish fly". Medically, cantharidin is classified as a vesicant, a substance that causes blistering of the skin. When applied topically, it triggers the release of certain enzymes that lead to the separation of epidermal cells. This process, known as acantholysis, causes a blister to form underneath the skin lesion. As the blister heals, the lesion is removed along with the fluid. This unique mechanism makes it an effective tool in dermatology for treating certain skin growths.

Cantharidin vs. Brand-Name Ycanth

For many years, cantharidin was not an FDA-approved drug in the United States and was only available through specialty compounding pharmacies for off-label uses. This changed in July 2023 when the FDA approved the brand-name product Ycanth, which contains a proprietary formulation of cantharidin. The approval marked the first official, FDA-sanctioned treatment for molluscum contagiosum. It's important to understand the distinction:

  • Generic Name (Cantharidin): Refers to the active chemical compound itself.
  • Brand Name (Ycanth): Refers to the FDA-approved product containing cantharidin, developed and marketed by Verrica Pharmaceuticals.
  • Generic Availability: A generic product is a therapeutically equivalent, typically less expensive version of a brand-name drug that becomes available after the brand's patent expires. For cantharidin, there is no generic product available on the market yet.

The Role of Compounded Cantharidin

Before the FDA approval of Ycanth, dermatologists often relied on compounded cantharidin preparations to treat warts and molluscum contagiosum. Compounding pharmacists would create custom formulations, sometimes combining cantharidin with other agents like salicylic acid and podophyllotoxin. While these compounded formulations were used successfully for decades, their use was considered off-label and not subject to the same rigorous testing and FDA oversight as Ycanth. Ycanth's approval provides a standardized, FDA-regulated product for healthcare providers to use.

Comparing Ycanth (Brand) and Compounded Cantharidin

Feature Ycanth (Brand) Compounded Cantharidin
FDA Approved Yes, in July 2023 for molluscum contagiosum. No, historically used off-label based on physician discretion.
Availability Prescription-only brand-name product. Prepared by specialty compounding pharmacies upon prescription.
Formulation Standardized 0.7% solution delivered via a single-use applicator. Customizable concentration, often mixed with other agents.
Purpose Specifically indicated for molluscum contagiosum. Used for various dermatological conditions, including warts and molluscum.
Regulation Regulated by the FDA for safety and efficacy. Not subject to FDA approval for the compounded product itself.

Who Can Administer Cantharidin?

Due to its potential toxicity and vesicant properties, cantharidin must be administered by a qualified healthcare professional, such as a dermatologist. The product is not dispensed to the patient for at-home use. During an in-office visit, the healthcare provider carefully applies a small amount of the solution directly to each lesion. The patient is then typically instructed to wash off the medication with soap and water after a specific period, usually 24 hours.

Potential Side Effects

As with any medication, cantharidin use can cause side effects. The most common adverse reactions occur at the application site and may include:

  • Blistering
  • Pain and itching
  • Redness (erythema)
  • Scabbing or crusting
  • Discoloration
  • Dryness or erosion of the skin

Severe complications, including life-threatening toxicity, can occur if cantharidin is accidentally ingested. It is also highly toxic to the eyes, and accidental exposure can lead to severe injury, and in rare cases, blindness. For these reasons, strict protocols are followed during and after application to ensure safety.

Conclusion

In summary, the generic name for the active ingredient in the FDA-approved brand-name drug Ycanth is cantharidin. As of today, there is no generic product available in the U.S. market that is a therapeutically equivalent alternative to Ycanth. Ycanth is the first and only FDA-approved formulation, specifically for molluscum contagiosum. Before its approval, cantharidin was available through compounding pharmacies for the treatment of warts and molluscum, but these preparations were not subject to the same level of FDA oversight. Patients seeking cantharidin treatment must receive it from a healthcare professional, who will determine the appropriate brand or compounded option based on the condition being treated and local availability.

For more information on the FDA approval of Ycanth, please refer to the official FDA announcement from 2023.

Frequently Asked Questions

Cantharidin is the generic name for the active ingredient found in the brand-name medication Ycanth. Ycanth is a specific, FDA-approved formulation of cantharidin, whereas cantharidin itself is the chemical compound.

A generic version of a drug becomes available after the brand's patent expires. Since Ycanth was just approved by the FDA in 2023, its patent is still active, and a therapeutically equivalent generic product is not yet permitted to be manufactured in the U.S..

No, cantharidin is a prescription-only medication that must be applied by a healthcare provider. It is not available for purchase over the counter due to its vesicant properties and risk of serious harm if used improperly.

Ycanth (cantharidin) is FDA-approved for the topical treatment of molluscum contagiosum in adults and children aged two and older.

Historically, compounded versions of cantharidin have been used by dermatologists to treat common warts, plantar warts, and periungual warts. However, the brand-name product Ycanth is currently only FDA-approved for molluscum contagiosum.

The most common side effects are local skin reactions at the application site, including blistering, pain, itching, redness, scabbing, and discoloration.

Some healthcare providers may still use compounded cantharidin formulations, particularly for conditions like warts. However, Ycanth is the only FDA-regulated and standardized option for molluscum contagiosum.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.