Regeneron and Intellia's Gene Therapy Study for Hemophilia B: A Potential Breakthrough

Thursday, Aug 14, 2025 5:58 am ET1min read

Regeneron Pharmaceuticals and Intellia Therapeutics are conducting a clinical study to evaluate the safety and effectiveness of a gene insertion therapy for individuals with hemophilia B. The therapy aims to enable the body to produce clotting factor IX, potentially reducing the need for regular factor replacement therapy. Positive outcomes could impact the stock performance of both companies and position them as leaders in hemophilia treatment.

Regeneron Pharmaceuticals and Intellia Therapeutics are conducting a clinical study to evaluate the safety and effectiveness of a gene insertion therapy for individuals with hemophilia B. The therapy aims to enable the body to produce clotting factor IX, potentially reducing the need for regular factor replacement therapy. Positive outcomes could impact the stock performance of both companies and position them as leaders in hemophilia treatment.

Hemophilia B is an X-linked coagulation disorder characterized by low or dysfunctional Factor IX (FIX). Currently, hemophilia B is treated by FIX replacement therapy with plasma-derived or recombinant products. Gene therapy (GT) has been developed as an alternative treatment, using adeno-associated viral vectors (AAVV) to transfer genetic material into liver cells. Clinical trials have shown that GT is effective in sustaining plasma levels of FIX and reducing bleeding [2].

Regeneron Pharmaceuticals is advancing the hemophilia B program, with Intellia eligible for milestones and royalties. The companies are collaborating to develop this innovative modular platform capability. Positive results from this clinical study could significantly impact their stock prices and market position.

The stock performance of Regeneron Pharmaceuticals has been affected by a recent class action lawsuit alleging that the company inflated Medicare reimbursements by failing to include certain discounts in Eylea’s pricing calculations. The lead plaintiff was appointed on January 7, 2025, and investors are advised to monitor updates and potential recovery options [1].

Investors should closely follow the progress of this clinical trial, as successful outcomes could lead to significant market gains for both Regeneron Pharmaceuticals and Intellia Therapeutics.

References:
[1] https://www.tradingview.com/news/11thestate:540f00ec7094b:0-lead-plaintiff-appointed-in-regeneron-pharmaceuticals-class-action/
[2] https://pubmed.ncbi.nlm.nih.gov/40795181/

Regeneron and Intellia's Gene Therapy Study for Hemophilia B: A Potential Breakthrough

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