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Vesemnogene lantuparvovec - Lantu Biopharma

Drug Profile

Vesemnogene lantuparvovec - Lantu Biopharma

Alternative Names: AAV-hSMN1

Latest Information Update: 29 Jul 2024

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At a glance

  • Originator Lantu Biopharma
  • Class Gene therapies; Spinal muscular atrophy gene therapies
  • Mechanism of Action Gene transference; Survival of motor neuron 1 protein replacements
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity No

Highest Development Phases

  • Phase I/II Spinal muscular atrophy

Most Recent Events

  • 19 Jul 2024 Phase-I/II clinical trials in Spinal muscular atrophy (In children, In adults) in China (IV) (NCT06288230)
  • 01 Mar 2024 Preclinical trials in Spinal muscular atrophy in China (Parenteral)
  • 01 Mar 2024 Lantu Biopharma plans a phase I/II trial for Spinal muscular atrophy (IV) in March 2024 (NCT06288230)

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