Wells Fargo 21st Annual Healthcare Conference
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Altimmune (ALT) Wells Fargo 21st Annual Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Altimmune Inc

Wells Fargo 21st Annual Healthcare Conference summary

22 Sep, 2026

Strategic focus and clinical progress

  • Transitioned to a late-stage development company with a primary focus on liver diseases, especially MASH, using the balanced glucagon/GLP-1 agonist pemvidutide.

  • Phase III PERFORMA trial for MASH is actively enrolling, following positive phase II data and strengthened financials to support execution.

  • Positive phase II results in alcohol use disorder (AUD) highlight pemvidutide's potential across multiple liver-related indications.

  • Emphasis on differentiation through dual action on liver and metabolic pathways, aiming for better adherence and patient outcomes.

  • Ongoing efforts to expand into additional indications, including alcohol-related liver disease (ALD), with phase II trials fully enrolled.

Clinical trial design and differentiation

  • PERFORMA phase III uses biopsy endpoints and innovative AI-assisted biopsy reading to reduce variability and facilitate enrollment.

  • Study includes two cohorts and tests both 1.8 mg and 2.4 mg doses, with simple titration and strong tolerability.

  • Focus on classic efficacy markers, adherence rates, and muscle mass preservation, with MRI used for body composition analysis.

  • Data readout for PERFORMA expected in 2029, with accelerated approval data at 52 weeks.

  • Differentiation from competitors highlighted by lower discontinuation rates and balanced dual agonism.

Market opportunity and regulatory strategy

  • Addressing high unmet needs in MASH, AUD, and ALD, with a U.S. target population of 12 million for moderate to severe AUD and 6 million for ALD.

  • Planning phase III for AUD, targeting both typical AUD and those with overlapping ALD, with regulatory engagement underway.

  • RESTORE phase II ALD trial uses FibroScan as a primary endpoint, with 12-month data readout planned.

  • Regulatory strategy includes end-of-phase II meetings with FDA and European agencies for both MASH and AUD.

  • Strong financial position with $519 million in cash, supporting operations through MASH readout in 2029; additional funding options considered for AUD phase III.

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