Welcome to our dedicated page for Madrigal Pharmac news (Ticker: MDGL), a resource for investors and traders seeking the latest updates and insights on Madrigal Pharmac stock.
Madrigal Pharmaceuticals, Inc. (MDGL) is a clinical-stage biopharmaceutical company pioneering treatments for metabolic dysfunction-associated steatohepatitis (MASH), including its FDA-approved therapy Rezdiffra. This page provides investors and healthcare professionals with timely updates on corporate milestones, clinical research, and regulatory developments.
Access the latest press releases, earnings reports, and scientific announcements in one centralized location. Key updates include Rezdiffra's commercialization progress, new clinical data analyses, and strategic partnerships advancing MASH treatment innovation. Our curated news collection ensures you stay informed about material events without speculative commentary.
Regular updates cover regulatory submissions, trial expansions, financial disclosures, and patient access initiatives. Content is rigorously verified to provide accurate, actionable information for investment and therapeutic decision-making. Bookmark this page to monitor Madrigal's progress in addressing critical unmet needs in liver disease therapeutics.
Madrigal Pharmaceuticals (Nasdaq: MDGL) has announced its participation in the H.C. Wainwright 8th Annual MASH Virtual Investor Conference. The event will feature a fireside chat scheduled for 2:00 P.M. ET on Monday, Oct. 7, 2024. The session will be webcast live and can be accessed through a provided link or via Madrigal's Investor Relations Events page. A replay of the webcast will be available after the event.
Madrigal Pharmaceuticals (Nasdaq: MDGL) has appointed Dr. Michael R. Charlton as Senior Vice President, Clinical Development, effective October 1, 2024. Dr. Charlton brings over 30 years of leadership experience in hepatology, gastroenterology, and liver transplantation, with particular expertise in NASH. He has held academic leadership roles at Mayo Clinic, University of Chicago, and Intermountain Medical Center.
Dr. Charlton's extensive research in NASH has resulted in over 200 publications, including authoring guidelines for the American Association for the Study of Liver Diseases. His appointment reflects Madrigal's commitment to innovation in NASH R&D, following the development of their breakthrough therapy, Rezdiffra (resmetirom).
Madrigal Pharmaceuticals (NASDAQ:MDGL) has announced the publication of positive patient-reported outcomes data from the Phase 3 MAESTRO-NASH trial of Rezdiffra™ (resmetirom) in Hepatology. The study showed that Rezdiffra, the first FDA-approved medication for NASH, improved health-related quality of life (HRQL) in patients with moderate to advanced fibrosis.
Key findings include:
- Clinically meaningful and statistically significant improvements in emotional well-being and health distress
- Positive tolerability profile of Rezdiffra
- Improvements in multiple HRQL domains, including Worry, Health Distress, and Stigma
- No worsening of HRQL related to potential side effects
Rezdiffra is a once-daily, oral, liver-directed thyroid hormone receptor (THR)-β agonist indicated for treating adults with noncirrhotic NASH with moderate to advanced liver fibrosis.
Madrigal Pharmaceuticals (Nasdaq: MDGL) has announced its participation in the Morgan Stanley 22nd Annual Global Healthcare Conference. The event is scheduled for Thursday, September 5, 2024, at 10:45 A.M. ET. Investors and interested parties can access the live webcast of Madrigal's presentation through a provided link or by visiting the company's Investor Relations Events page.
This conference participation offers an opportunity for Madrigal to showcase its latest developments and engage with the investment community. The company's involvement in such a prestigious healthcare event highlights its commitment to transparency and shareholder communication. For those unable to attend the live presentation, a replay of the webcast will be made available after the event, ensuring widespread access to the information shared during the conference.
Madrigal Pharmaceuticals (NASDAQ:MDGL) reported Q2 2024 financial results and corporate updates. Key highlights include:
- Net sales of $14.6 million for Rezdiffra™ (resmetirom)
- Rezdiffra coverage for over 50% of commercial lives; less than 5% require biopsy
- Expert guidelines recommend Rezdiffra as first-line therapy for F2/F3 NASH/MASH patients
- Plans to directly commercialize resmetirom in Europe following expected EMA decision mid-2025
- Cash, cash equivalents, restricted cash, and marketable securities of $1.1 billion as of June 30, 2024
The company reported strong initial U.S. launch progress for Rezdiffra, with high enthusiasm from physicians and patients. New data presented at EASL Congress showed 91% efficacy in halting or improving liver stiffness at three years. Madrigal aims to expand its global leadership in NASH treatment.
Madrigal Pharmaceuticals (NASDAQ:MDGL) has appointed Shannon Kelley as General Counsel, effective August 5, 2024. Kelley, who joined Madrigal in 2024 as Chief Compliance Officer, brings over 20 years of healthcare legal and compliance experience. Previously, she held senior roles at Sanofi and Boston Scientific , and worked in enforcement roles with the U.S. Federal Government.
CEO Bill Sibold praised Kelley's leadership and expertise, highlighting her instrumental role in guiding the company through rapid growth. Kelley expressed enthusiasm about Madrigal's opportunity to deliver groundbreaking therapy for nonalcoholic steatohepatitis (NASH), the leading cause of liver transplantation in women in the U.S. She aims to be a strategic partner in building an industry-leading company with a strong culture of ethics and integrity.
Madrigal Pharmaceuticals (Nasdaq: MDGL) has announced the release date for its second-quarter 2024 financial results. The company will disclose the results on Wednesday, August 7, 2024, before the U.S. financial markets open. Following this, Madrigal's management will host a live webcast at 8 a.m. Eastern Time to review the financial and operating results.
Investors and interested parties can access the webcast through the Investor Relations section of Madrigal Pharmaceuticals' website. To ensure a smooth connection, participants are advised to register at least 15 minutes before the scheduled start. The webcast will remain available for approximately two hours after the live event concludes.
Madrigal Pharmaceuticals announced new data from the Phase 3 MAESTRO-NASH study of Rezdiffra™ (resmetirom) at the EASL Congress.
The study showed Rezdiffra improved key fibrotic features predictive of cirrhosis. AI-driven analysis revealed that 80% of patients treated with Rezdiffra experienced fibrosis improvement or stabilization. In noninvasive tests over three years, 91% showed improved or stable liver stiffness.
Health-related quality of life metrics also improved, including reductions in worry, health distress, and stigma. Additionally, Rezdiffra had positive outcomes in patients with Metabolic Dysfunction and Alcohol-Associated Liver Disease (MetALD).
The data supports Rezdiffra as a foundational therapy in NASH, demonstrating durable responses and broad treatment benefits.
Madrigal Pharmaceuticals (Nasdaq: MDGL) will participate in the Goldman Sachs 45th Annual Global Healthcare Conference on June 11, 2024. The company will present at 8:40 A.M. ET, with the presentation webcast live on Madrigal’s Investor Relations Events page. A replay of the webcast will be available post-event. This participation reflects Madrigal's engagement with key industry stakeholders and potential investors.
Madrigal Pharmaceuticals, a biopharma company specializing in NASH treatment, will present ten data abstracts at the EASL Congress from June 5-8, 2024, in Milan.
The presentations will focus on Rezdiffra™ (resmetirom), a novel THR-β agonist and the first approved NASH therapy. Highlights include new Phase 3 MAESTRO data on quality of life, noninvasive test results, and Rezdiffra's efficacy in MetALD patients.
Additionally, Madrigal will showcase real-world data on NASH's human and economic impact, noting faster progression to severe liver conditions than previously thought.
Rezdiffra has shown significant efficacy in improving or stabilizing fibrosis in 80% of patients and is indicated for noncirrhotic NASH with moderate to advanced fibrosis. Continued approval hinges on ongoing confirmatory trials.
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