Theratechnologies Addresses EGRIFTA SV Shortage Concerns

Understanding the EGRIFTA SV® Supply Shortage

As concerns mount regarding the availability of EGRIFTA SV® (tesamorelin for injection), Theratechnologies Inc. has provided an essential update about the situation. This biopharmaceutical company focuses on developing and commercializing innovative therapies, particularly for those affected by unmet medical needs. The anticipated shortage of EGRIFTA SV® is set to impact patients by mid-January due to an unexpected shutdown of the contract manufacturing facility in the preceding year. Although some pharmacies across the United States still have limited supplies available, numerous clinics and pharmacies are already facing stock shortages.

Regulatory Updates from Theratechnologies

In response to the anticipated shortage, Theratechnologies promptly filed a Prior Approval Supplement (PAS) with the U.S. Food and Drug Administration (FDA) on December 18. This filing signifies their commitment to obtaining quick resolution and regulatory approval for new batches of EGRIFTA SV®. Additionally, the company has taken proactive steps by requesting a Type D meeting to clarify the manufacturing status of their latest production. The FDA has assured that they will respond to the inquiries regarding these batches by early February.

Commitment to Patients

Theratechnologies' dedication to patients relying on EGRIFTA SV® is unwavering. As the only FDA-approved treatment of its type, the company emphasizes the importance of this therapy for individuals living with HIV. Dr. Christian Marsolais, the Senior Vice President and Chief Medical Officer of Theratechnologies, has publicly reiterated the company’s commitment to collaborating with the FDA to expedite the release of new medication batches. Their intent is to ensure that patients receive the vital treatment they need without unnecessary delays.

Preparedness for Future Developments

While addressing the immediate supply concerns, Theratechnologies also communicated their intent to keep the market informed about any significant developments. The current situation highlights not only the challenges of drug manufacturing and supply but also Theratechnologies' proactive stance to mitigate these impacts. Consistent updates will ensure that healthcare providers and patients remain informed as the situation unfolds.

The Importance of EGRIFTA SV®

EGRIFTA SV® is crucial for managing abdominal fat in people living with HIV, addressing a crucial aspect of their health and quality of life. This situation underscores the importance of efficient drug delivery and continuous availability of critical medications to support patients’ long-term health goals. Recognizing this, Theratechnologies is working diligently to restore the necessary supply levels.

Looking Ahead

The journey of navigating regulatory processes amidst a supply challenge can be complex. However, Theratechnologies is prioritizing clear communication with stakeholders including patients, healthcare providers, and investors about the status of EGRIFTA SV®. The company is aware of the potential implications of this shortage not only for those directly affected but also for its overall business and financial standing.

As the FDA's response deadline approaches, anticipation builds around the next steps the company will be able to take regarding the PAS and the EGRIFTA SV® batches. Theratechnologies is confident in its strategy and efforts to remedy the challenges at hand while staying true to its mission of enhancing the lives of those impacted by HIV.

Frequently Asked Questions

What caused the shortage of EGRIFTA SV®?

The shortage is primarily due to a voluntary shutdown of the manufacturing facility that produced EGRIFTA SV®.

When is the anticipated impact of the shortage expected to be felt?

The supply shortage is expected to impact patients by mid-January as pharmacies begin reporting stockouts.

What steps is Theratechnologies taking to address the shortage?

The company filed a Prior Approval Supplement with the FDA and has requested a Type D meeting to expedite the review of new batches.

How does EGRIFTA SV® benefit patients with HIV?

EGRIFTA SV® is the only FDA-approved therapy that helps manage abdominal fat in people living with HIV, which is often a significant health concern.

What future updates can we expect from Theratechnologies?

Theratechnologies intends to keep the market informed with consistent updates regarding the status of EGRIFTA SV® and any related developments.

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