Skip to content

What is Corifollitropin A? Understanding this Long-Acting Fertility Medication

4 min read

A single injection of corifollitropin alfa can replace seven days of daily FSH shots in fertility treatment protocols, offering a more convenient patient experience. What is Corifollitropin A? It is a long-acting recombinant hormone primarily used for controlled ovarian stimulation (COS) during assisted reproductive technologies (ART), such as in vitro fertilization (IVF).

Quick Summary

Corifollitropin alfa (Elonva) is a long-acting injectable hormone that stimulates follicle growth, simplifying the first week of ovarian stimulation in IVF cycles by reducing injection frequency.

Key Points

  • Long-Acting FSH: Corifollitropin A is a recombinant FSH with a prolonged half-life, allowing for less frequent dosing.

  • Single Injection Protocol: One subcutaneous injection can replace seven daily FSH shots for the first week of controlled ovarian stimulation.

  • Improved Patient Convenience: Reduced injection frequency lowers patient burden and psychological stress during fertility treatments like IVF.

  • Equivalent Efficacy: Clinical studies show that corifollitropin alfa offers similar ongoing pregnancy rates to daily FSH regimens in normal responders.

  • Requires Patient Monitoring: Close monitoring for ovarian response and risk of Ovarian Hyperstimulation Syndrome (OHSS) is necessary, especially in high-risk patients.

  • Dosage Considerations: The appropriate dosage is determined by a healthcare professional based on individual patient characteristics.

  • Not FDA Approved (As of 2014): While available in many countries under the brand name Elonva, a 2014 FDA Complete Response Letter indicates it may not be approved in the U.S..

In This Article

Before discussing Corifollitropin A, it is important to note that information provided here is for general knowledge only and should not be taken as medical advice. Always consult with a healthcare provider before starting any new medication or treatment.

What Exactly is Corifollitropin A?

Corifollitropin A, also known by its active substance name corifollitropin alfa (brand name Elonva), is a cutting-edge recombinant follicle-stimulating hormone (FSH) agonist. Unlike conventional FSH, which has a short half-life and requires daily injections, corifollitropin alfa is engineered to have a prolonged effect in the body. This is achieved through a genetic modification process using recombinant DNA technology. A specialized C-terminal peptide (CTP) from the beta-subunit of human chorionic gonadotropin (hCG) is fused to the beta-subunit of human FSH. This structural change increases its circulating lifetime significantly, leading to a much longer half-life of approximately 65–69 hours compared to traditional FSH preparations.

How Does Corifollitropin A Work?

Corifollitropin A's primary function is to stimulate the ovaries to produce multiple follicles, a necessary step for successful IVF and other ART treatments. Its mechanism of action centers on its unique pharmacokinetic properties, which allow it to provide sustained FSH activity from a single injection. The medication binds to the same FSH receptors as endogenous FSH, but its extended half-life ensures that serum FSH levels remain above the threshold required for sustained follicular growth for a full seven days.

The Mechanism of Action in Detail

  • Long-acting nature: The addition of the CTP to the FSH molecule is the key to its prolonged action. This modification slows down the rate of metabolic clearance, meaning the drug stays in the bloodstream longer than conventional FSH.
  • Rapid peak, slow decline: Following a single subcutaneous injection, the serum concentration of corifollitropin alfa peaks within 1–2 days and then slowly declines, maintaining therapeutic levels of FSH for a week.
  • Targeted stimulation: Corifollitropin alfa interacts exclusively with the FSH receptor and lacks any luteinizing hormone (LH) activity, ensuring a focused and controlled stimulation of the follicles.

Primary Uses in Fertility Treatment

Corifollitropin A is used in specific protocols for patients undergoing ART procedures. It is most commonly administered as part of a gonadotropin-releasing hormone (GnRH) antagonist protocol, which is designed to prevent premature ovulation. This allows for the synchronized growth of multiple follicles before the eggs are retrieved.

Key applications include:

  • Controlled Ovarian Stimulation (COS): In women participating in ART programs, a single injection of corifollitropin alfa can initiate and sustain multifollicular development for the first seven days of treatment.
  • Hypogonadotropic Hypogonadism in Adolescent Males: In combination with human chorionic gonadotropin (hCG), corifollitropin alfa can be used in adolescent males aged 14 and older with delayed puberty due to hypogonadotropic hypogonadism, to stimulate testicular growth.

Corifollitropin A vs. Daily FSH: A Comparison

To understand the benefits of corifollitropin A, it's helpful to compare it with the more traditional daily recombinant FSH (rFSH) regimens. The key difference lies in the injection frequency and overall treatment convenience.

Feature Corifollitropin A Daily Recombinant FSH (rFSH)
Injection Frequency Single injection replaces seven daily shots. Requires daily injections for 8–12 days or more.
Half-Life Long, approximately 65–69 hours. Short, requiring frequent dosing to maintain therapeutic levels.
Patient Convenience High, significantly reduces number of injections and patient burden. Lower, multiple daily injections can cause stress and potential for missed doses.
Dosage Adjustment Dose is based on patient characteristics, with limited mid-cycle adjustment in the first 7 days. Flexible daily dosing allows for fine-tuning based on ovarian response.
Efficacy Comparable live birth and ongoing pregnancy rates in normal responders. Well-established efficacy in various patient groups.
Risk of OHSS Risk is comparable to daily FSH, but caution needed in potential hyper-responders due to sustained effect. Managed by adjusting daily doses based on monitoring.

Potential Side Effects and Safety Considerations

As with any fertility medication, corifollitropin alfa carries potential side effects and risks. A crucial aspect of treatment is proper patient selection and careful monitoring by a physician experienced in infertility treatment.

Common Side Effects

  • Injection site reactions (pain, redness, swelling)
  • Headache
  • Nausea and pelvic discomfort
  • Breast tenderness

Serious Adverse Events

  • Ovarian Hyperstimulation Syndrome (OHSS): This is a significant risk with all ovarian stimulation protocols. The sustained nature of corifollitropin alfa's effect requires careful management, particularly in women identified as potential high responders. Severe OHSS can lead to complications such as blood clots or fluid accumulation.
  • Thromboembolism: Blood clot formation has been reported, particularly in women with pre-existing risk factors.
  • Multiple Pregnancy: ART increases the risk of multiple pregnancies, and corifollitropin alfa can contribute to this by stimulating multiple follicles.
  • Contraindications: The drug is not suitable for women with certain conditions, including tumors of reproductive organs or hypothalamus/pituitary, unexplained abnormal vaginal bleeding, primary ovarian failure, or certain risk factors for OHSS.

Patient Experience and Practical Advantages

The primary motivation for developing corifollitropin alfa was to create a more patient-friendly experience. The reduction from daily injections to a single shot for the initial week of stimulation can dramatically decrease the stress and anxiety associated with self-administering medication. This simplified protocol can also minimize the risk of administration errors, which is critical for ensuring consistent hormonal levels. Clinical trials have consistently shown that corifollitropin alfa provides equivalent efficacy to daily rFSH regimens in terms of ongoing pregnancy rates in normal responders, validating its use as a viable and convenient alternative.

Conclusion

Corifollitropin A (alfa) is a highly effective, long-acting recombinant FSH that simplifies the process of ovarian stimulation for women undergoing ART procedures. By condensing the first week of daily injections into a single, subcutaneous dose, it significantly improves patient convenience and comfort without compromising efficacy in well-selected patients. While it offers substantial practical advantages over conventional daily FSH, its use requires careful patient assessment and monitoring, especially regarding the risk of OHSS in high responders. This innovative medication continues to play an important role in modern reproductive medicine by enhancing the patient experience during complex fertility treatments.

For more comprehensive information on corifollitropin alfa, a good resource is the European Medicines Agency's public assessment report on the brand product, Elonva.

Frequently Asked Questions

The brand name for corifollitropin alfa is Elonva.

For controlled ovarian stimulation in IVF, corifollitropin A is typically administered as a single subcutaneous injection, which provides sustained activity for a full seven days.

The main advantage is patient convenience, as a single injection replaces seven days of daily shots, reducing the burden and stress associated with frequent injections.

A significant risk is the development of Ovarian Hyperstimulation Syndrome (OHSS), particularly in women who are predicted to be high responders. Careful patient selection and monitoring are necessary.

Yes, clinical trials have shown that corifollitropin alfa is non-inferior to daily recombinant FSH in terms of achieving comparable ongoing pregnancy rates in appropriate patients.

Yes, in combination with hCG, it is indicated for treating hypogonadotropic hypogonadism in adolescent males (14 years and older).

The appropriate dose of Corifollitropin A is determined by a healthcare professional based on individual patient factors.

In 2014, the U.S. FDA issued a Complete Response Letter for its New Drug Application, and it is primarily marketed in countries in the EU and elsewhere.

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7

Medical Disclaimer

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