AMT-130

Product

Last mentioned: Mar 3, 2026

Timeline

  1. Type B FDA Meeting Target

    Planned follow-up to define Phase III and regulatory path for AMT-130.

  2. AMT-260 Data Readout

    Expected clinical data from Phase I/IIa epilepsy study in H1 2026.

  3. Type A FDA Meeting

    Discussed AMT-130 approval pathway; alignment not yet reached.

  4. Fiscal Year End

    Closed 2025 with $622.5 million in liquidity.

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