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COMPANY

Intrinsic Therapeutics

HQ: Woburn, MA source · barricaid.com ↗

FDA-cleared device company Clinical Phase 3

Location: Woburn, MA · source · Dec 8, 2023

Profile checked Oct 10, 2026

Keywords: Lumbar Disc Herniation Annular Tear of Lumbar Disc Lumbar Disc Herniation Surgery Disc Herniation Annular Disc Tear Lumbar Spine Disc Herniation Anular Tear of Lumbar Disc Barricaid Annular closure

9Trials (company is sponsor)

Timeline

  1. Trial start Phase 4: Return to Activity After Surgery for Lumbar Disc Herniation source ↗
  2. Trial start —: PMCFU of an Annular Closure System source ↗
  3. Trial start —: Incidence of Large Annular Defects in Primary Lumbar Discectomy Patients source ↗
  4. Trial start Not phased (device or behavioral study): Study of Lumbar Discectomy With Annular Closure source ↗
  5. Trial start Phase 4: A Post Marketing Surveillance Study source ↗
  6. Trial start —: Post-Marketing Clinical Follow-Up of a Spine Implant source ↗
  7. Trial start —: Lumbar Discectomy Control Study, Risk Factors for Reherniation source ↗
  8. Trial start Phase 4: A Prospective, Randomized, Multicenter Study to Demonstrate the Superiority of the Barricaid to Discectomy for Primary Lumbar Disc Herniation source ↗
  9. Trial start Not phased (device or behavioral study): Barricaid EU Post Market Study for Primary Lumbar Disc Herniation source ↗

Upcoming milestones

Estimated primary completion per ClinicalTrials.gov. Dates move.

Clinical trials (lead sponsor) 9

RecordTitlePhaseStatusStartPrimary completion
NCT07667348Return to Activity After Surgery for Lumbar Disc HerniationPhase 4Not yet recruitingJun 30, 2026Oct 1, 2027 (estimated)
NCT03366779A Post Marketing Surveillance StudyPhase 4Unknown status (ClinicalTrials.gov)Jan 16, 20182024-06 (estimated)
NCT05467072PMCFU of an Annular Closure SystemNot listedUnknown status (ClinicalTrials.gov)Sep 27, 20232024-10 (estimated)
NCT03180749Post-Marketing Clinical Follow-Up of a Spine ImplantNot listedUnknown status (ClinicalTrials.gov)Mar 2, 20172024-06 (estimated)
NCT03986580Study of Lumbar Discectomy With Annular ClosureNot phased (device or behavioral study)Unknown status (ClinicalTrials.gov)May 1, 20202024-06 (estimated)
NCT01283438A Prospective, Randomized, Multicenter Study to Demonstrate the Superiority of the Barricaid to Discectomy for Primary Lumbar Disc HerniationPhase 4Unknown status (ClinicalTrials.gov)Dec 17, 20102016-10 (actual)
NCT02477176Lumbar Discectomy Control Study, Risk Factors for ReherniationNot listedUnknown status (ClinicalTrials.gov)Feb 17, 20162024-03 (estimated)
NCT01534065Barricaid EU Post Market Study for Primary Lumbar Disc HerniationNot phased (device or behavioral study)Completed2009-042013-03 (actual)
NCT03252691Incidence of Large Annular Defects in Primary Lumbar Discectomy PatientsNot listedWithdrawn2020-092021-04 (estimated)
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