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A prospective, randomised, double-blinded, placebo-controlled study investigating the safety and tolerability of STA363 in patients with radiculopathy caused by lumbar disc herniation

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A prospective, randomised, double-blinded, placebo-controlled study investigating the safety and tolerability of STA363 in patients with radiculopathy caused by lumbar disc herniation

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 03 Oct 2024

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At a glance

  • Drugs Lactic acid (Primary)
  • Indications Intervertebral disc displacement
  • Focus Adverse reactions
  • Sponsors Stayble Therapeutics

    • Most Recent Events

    • 03 Oct 2024 Status changed from recruiting to completed.
    • 09 May 2023 According to a Stayble Therapeutics media release, first patient is planned to be treated in Q3 2023.
    • 14 Apr 2023 Status changed from planning to recruiting.

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