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FDA approves higher dose of Catalyst's LEMS drug

EditorBrando Bricchi
Published 2024-05-30, 02:12 p/m
CPRX
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CORAL GABLES, Fla. - Catalyst Pharmaceuticals, Inc. (NASDAQ: CPRX), a commercial-stage biopharmaceutical company, announced today that the U.S. Food and Drug Administration (FDA) has approved an increased maximum daily dose of FIRDAPSE (amifampridine) for the treatment of Lambert-Eaton myasthenic syndrome (LEMS). The new dosage extends the maximum daily dose for adults and pediatric patients weighing more than 45 kg from 80 mg to 100 mg.

LEMS is a rare autoimmune disorder that leads to muscle weakness and fatigue. FIRDAPSE, the only FDA-approved treatment for LEMS in the United States, functions by boosting acetylcholine release at neuromuscular junctions, which aids in improving muscle function in those affected by the disease. This approval provides healthcare providers and patients with additional flexibility in managing the condition.

Richard J. Daly, President and CEO of Catalyst, expressed the company's commitment to addressing the needs of LEMS patients and healthcare providers, highlighting the approval as a significant step that aligns with their mission to optimize patient outcomes.

The Catalyst Pathways Patient Assistance Program for FIRDAPSE offers support to families throughout their treatment journey, including access to a dedicated team for eligible patients. Healthcare professionals and caregivers can obtain more information by contacting the program or visiting the company's website.

Catalyst Pharmaceuticals continues to focus on developing and commercializing innovative treatments for rare and difficult-to-treat diseases. Alongside FIRDAPSE, the company holds commercial rights to FYCOMPA (perampanel) for epilepsy treatment and has recently launched AGAMREE (vamorolone) for Duchenne Muscular Dystrophy in the United States.

The information in this article is based on a press release statement from Catalyst Pharmaceuticals.

InvestingPro Insights

Catalyst Pharmaceuticals' recent FDA approval for an increased maximum daily dose of FIRDAPSE is a testament to its dedication to enhancing patient care in the treatment of Lambert-Eaton myasthenic syndrome (LEMS). This commitment is also reflected in the company's financial health and growth prospects, as evidenced by data and insights from InvestingPro.

InvestingPro Tips suggest that Catalyst Pharmaceuticals (NASDAQ: CPRX) is expected to see net income growth this year, underscoring the company's potential for increased profitability. Additionally, the company is praised for holding more cash than debt on its balance sheet, which provides financial stability and flexibility. For readers interested in deeper analysis, there are a total of 10 InvestingPro Tips available at https://www.investing.com/pro/CPRX, which could further inform investment decisions.

From the InvestingPro Data, we can see that Catalyst Pharmaceuticals has a market cap of approximately $1.93 billion USD, indicating a solid position in the market. The company's revenue growth over the last twelve months as of Q1 2024 stands at an impressive 60.38%, showcasing its ability to expand in a competitive sector. Furthermore, the company's gross profit margin during the same period is 64.33%, suggesting efficient management and a strong ability to translate sales into profit.

Investors looking to capitalize on the potential of Catalyst Pharmaceuticals can use the coupon code PRONEWS24 to get an additional 10% off a yearly or biyearly Pro and Pro+ subscription, which includes additional tips that could further guide investment strategies.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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