Press Releases August 6, 2026 08:00 AM

Madrigal Pharmaceuticals to Participate in the Canaccord Genuity 45th Annual Growth Conference

Madrigal Pharmaceuticals to present at the Canaccord Genuity 46th Annual Growth Conference on August 11, 2026

By Caleb Monroe
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Madrigal Pharmaceuticals announced its participation in the Canaccord Genuity 46th Annual Growth Conference where it will present its latest developments. The company focuses on developing therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), with its drug Rezdiffra already approved in the US and Europe for treating MASH with moderate to advanced fibrosis. The ongoing Phase 3 trial evaluates Rezdiffra for compensated MASH cirrhosis.

Madrigal Pharmaceuticals to Participate in the Canaccord Genuity 45th Annual Growth Conference
MDGL
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Key Points

  • Madrigal Pharmaceuticals will present at the Canaccord Genuity 46th Annual Growth Conference on August 11, 2026.
  • The company is focused on developing treatments for MASH, a liver disease with high unmet medical need.
  • Rezdiffra (resmetirom) is approved in the US and Europe for MASH with moderate to advanced fibrosis, and a Phase 3 trial is ongoing for cirrhosis treatment.

CONSHOHOCKEN, Pa., Aug. 06, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) announced today that the company will participate in the Canaccord Genuity 46th Annual Growth Conference on Tuesday, Aug. 11, 2026 at 12:00 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

  • Clinical trial outcomes for the ongoing Phase 3 study could be uncertain and impact future approvals and market potential.
  • Regulatory risks related to further expansion of indications for Rezdiffra.
  • Market adoption risks associated with a novel therapeutic in the specialty biopharmaceutical sector.

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