Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 2025
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Coya Therapeutics (COYA) Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 2025 summary

Event summary combining transcript, slides, and related documents.

Logotype for Coya Therapeutics Inc

Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 2025 summary

8 Jul, 2026

Strategic focus and pipeline overview

  • Focus on innovative therapies for neurodegenerative diseases by targeting regulatory T cells to reduce neuroinflammation.

  • Pipeline includes COYA 301 (recombinant IL-2), COYA 302 (IL-2 + CTLA4), and COYA 303 (IL-2 + GLP-1 agonist).

  • COYA 302 is being advanced in ALS and frontotemporal dementia, with plans for Alzheimer's and Parkinson's indications.

  • Strategic partnership with Dr. Reddy's Laboratories for COYA 302 in ALS, covering most global markets and up to $700 million in milestone payments.

  • Cash position of $40 million as of October 31, 2023, supporting operations into 2026.

Clinical data and upcoming milestones

  • Proof-of-concept trials showed COYA 302 halted ALS progression at six months and stabilized cognitive decline in Alzheimer's.

  • Additional data from Alzheimer's trials showed positive impact on inflammatory markers and cytokines.

  • Phase 2B ALS trial to initiate later in 2024, with IND submission planned for Q2 2025.

  • Top-line results from frontotemporal dementia trial expected early in the second half of 2025, with IND submission by year-end.

  • Data on COYA 301 and GLP-1 synergy to be published in the coming months.

Scientific rationale and trial design

  • Approach centers on restoring Treg function to address neuroinflammation, a key driver in neurodegenerative diseases.

  • COYA 302 combines IL-2 and CTLA4 to increase Treg durability and suppressive function, providing synergistic neuroprotection.

  • ALS phase 2B trial will enroll 120 patients, placebo-controlled, with a six-month ALSFRS endpoint and crossover design.

  • All ALS genetic subtypes included; trial designed to balance standard-of-care therapies across arms.

  • NfL and other biomarkers will be key secondary endpoints, with potential for accelerated approval discussions.

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