Barclays 28th Annual Global Healthcare Conference
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MacroGenics (MGNX) Barclays 28th Annual Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for MacroGenics Inc

Barclays 28th Annual Global Healthcare Conference summary

12 Mar, 2026

Pipeline overview and strategy

  • Focus on next-generation antibody therapeutics for cancer, leveraging ADCs, T-cell engagers, and dual checkpoint inhibitors.

  • Three ADC programs: MGC026 (B7-H3), MGC028 (ADAM9), and MGC030 (undisclosed Topo 1 target), all advancing through clinical or preclinical stages.

  • Broad partnerships, notably with Gilead for T-cell engagers and ongoing openness to further collaborations.

  • Well-capitalized with over $190 million in cash and a history of securing non-dilutive capital and milestone payments.

  • 2026 highlighted as a pivotal year with multiple clinical data readouts and strategic updates expected.

ADC program developments

  • MGC026 (B7-H3 ADC) uses a site-specific linker and potent exatecan payload, showing robust internalization and no ILD observed to date.

  • Early clinical data indicate activity across multiple solid tumor types; two expansion cohorts are enrolling, with specific tumor types undisclosed.

  • MGC028 (ADAM9 ADC) is a second-generation molecule with improved safety, no ocular toxicity, and broad tumor expression; data expected in the second half of 2026.

  • MGC030 is a first-in-class Topo 1 ADC with strong preclinical data, IND planned for Q3 2026, and target not yet disclosed.

  • Strategic focus on less crowded tumor indications and potential for future partnerships to support late-stage development.

Lorigerlimab and dual checkpoint approach

  • Lorigerlimab targets PD-1 and CTLA-4, with over 300 patients dosed and promising early safety and efficacy signals.

  • Recent LINNET study in gynecologic cancers paused due to grade 4/5 adverse events, with ongoing FDA discussions and a partial clinical hold.

  • Mid-2026 update planned to address regulatory status, safety, efficacy, and future development strategy.

  • Considering alternative dosing and enhanced patient screening to mitigate adverse events.

  • Early data suggest full PD-1 receptor occupancy at lower doses, supporting dosing flexibility.

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