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A Phase II/III, Multicentre, 8-week Run-in Phase Followed by a 12-week, Prospective, Parallel-group, Double-blind, Randomized Withdrawal, Placebo-controlled Study, with a 52 Week Open Label Extension, to Evaluate the Efficacy and Safety of Daily 1.5 to 3.5 Mg Basimglurant in Patients with Pain Associated with Trigeminal Neuralgia with Suboptimal Response to Their Current Anti-pain Therapy.

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Trial Profile

A Phase II/III, Multicentre, 8-week Run-in Phase Followed by a 12-week, Prospective, Parallel-group, Double-blind, Randomized Withdrawal, Placebo-controlled Study, with a 52 Week Open Label Extension, to Evaluate the Efficacy and Safety of Daily 1.5 to 3.5 Mg Basimglurant in Patients with Pain Associated with Trigeminal Neuralgia with Suboptimal Response to Their Current Anti-pain Therapy.

Status: Active, no longer recruiting
Phase of Trial: Phase II/III

Latest Information Update: 23 Jul 2025

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At a glance

  • Drugs Basimglurant (Primary)
  • Indications Facial pain; Pain; Trigeminal neuralgia
  • Focus Adverse reactions; Registrational; Therapeutic Use
  • Acronyms LibraTN
  • Sponsors Noema Pharma

Most Recent Events

  • 11 Jul 2025 Planned primary completion date changed from 31 Oct 2025 to 31 Dec 2025.
  • 11 Jul 2025 Status changed from recruiting to active, no longer recruiting.
  • 25 Apr 2025 Planned End Date changed from 31 Jan 2026 to 1 Feb 2027.

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