Press Releases September 2, 2026 08:00 AM

Madrigal Pharmaceuticals to Participate in the  2026 Cantor Global Healthcare Conference

Madrigal Pharmaceuticals to present at the 2026 Cantor Global Healthcare Conference

By Derek Hwang
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MDGL

Madrigal Pharmaceuticals announced its participation in the 2026 Cantor Global Healthcare Conference where it will present its progress and pipeline advancements. The company specializes in treatments for metabolic dysfunction-associated steatohepatitis (MASH), highlighting its drug Rezdiffra, the first FDA and European Commission approved medication for MASH with moderate to advanced fibrosis.

Madrigal Pharmaceuticals to Participate in the  2026 Cantor Global Healthcare Conference
MDGL
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Key Points

  • Madrigal Pharmaceuticals will present at a prominent healthcare investor conference on Sept. 10, 2026.
  • Their lead drug, Rezdiffra (resmetirom), is FDA and European Commission approved for treating MASH with moderate to advanced fibrosis.
  • An ongoing Phase 3 outcomes trial is assessing Rezdiffra’s effectiveness for compensated MASH cirrhosis.
  • The announcement impacts the biotechnology and pharmaceutical sectors focused on liver disease treatments.

CONSHOHOCKEN, Pa., Sept. 02, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) announced today that the company will participate in the 2026 Cantor Global Healthcare Conference on Thursday, Sept. 10, 2026 at 1:00 P.M. EDT.

The presentation will be webcast live and may be accessed here or by visiting Madrigal’s Investor Relations Events and Presentations page. A replay of the webcast will be available after the event.

About Madrigal Pharmaceuticals
Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]


Risks

  • The Phase 3 outcomes trial results remain pending, and unfavorable results could impact future approval and sales.
  • Competition in the biotechnology sector for liver disease therapeutics may affect Madrigal’s market share.
  • Regulatory or market reception risks exist despite prior approvals, influencing commercialization potential.

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