Breaking News: Theratechnologies Takes Major Step Towards FDA Approval for EGRIFTA-SV Manufacturing Environment!

Breaking News: Theratechnologies Takes Major Step Towards FDA Approval for EGRIFTA-SV Manufacturing Environment!

MONTREAL, Dec. 18, 2024 (GLOBE NEWSWIRE) —

Theratechnologies Inc. (“Theratechnologies” or the “Company”) (TSX: TH) (NASDAQ: THTX), a biopharmaceutical company focused on the development and commercialization of innovative therapies, today announced that the Company has submitted a Prior Approval Supplement (PAS) to the U.S. Food and Drug Administration (FDA) describing the changes made to the manufacturing environment of the facility where EGRIFTA SV ® is produced. A PAS is reviewed by the FDA within four months of receipt and an approval is needed prior to the distribution of the recently manufactured batches of EGRIFTA SV ®.

Impact on Individuals:

This major step towards FDA approval for EGRIFTA-SV manufacturing environment can have a significant impact on individuals who are in need of innovative therapies such as EGRIFTA-SV. With FDA approval, individuals can gain access to a high-quality product that has met the stringent standards set by the regulatory body, ensuring efficacy and safety.

Impact on the World:

On a larger scale, the approval of EGRIFTA-SV manufacturing environment by the FDA can have a positive impact on the world. It signifies a step forward in the development and commercialization of innovative therapies, paving the way for advancements in the biopharmaceutical industry. The availability of FDA-approved treatments can benefit global healthcare systems and contribute to the overall well-being of society.

Conclusion:

Theratechnologies’ submission of a Prior Approval Supplement to the FDA for EGRIFTA-SV manufacturing environment marks a significant milestone in the Company’s journey towards FDA approval. This development not only has the potential to benefit individuals in need of innovative therapies but also has a broader impact on the world by contributing to advancements in the biopharmaceutical industry. As the FDA reviews the PAS and potentially approves the manufacturing environment changes, we can expect to see positive outcomes for both individuals and society as a whole.

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