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Eledon Pharmaceuticals

HQ: Irvine, CA source · eledon.com ↗ · West Coast

Clinical Phase 3

Eledon Pharmaceuticals develops tegoprubart, a product candidate based on CD40 Ligand biology. Eledon Pharmaceuticals is conducting clinical research on tegoprubart in kidney transplantation, islet cell transplantation and xenotransplantation. From company website Source · checked 2026-10-19

Eledon Pharmaceuticals is listed on ClinicalTrials.gov as the lead sponsor of 6 studies; the most recently updated is “Study of Tegoprubart Efficacy and Safety Compared With Tacrolimus in Kidney Transplantation” (Phase 3, not yet recruiting), in Kidney Transplant Rejection. From public records Source · 2026-10-12

Sources for this description (2)
  • Eledon Pharmaceuticals develops tegoprubart, a product candidate based on CD40 Ligand biology.
    • “Our focus on and deep understanding of the biology and Mechanism of Action of the CD40 Ligand have driven Eledon’s research and development of our lead product candidate tegoprubart.” https://eledon.com/science/pipeline/ (2026-10-19)
  • Eledon Pharmaceuticals is conducting clinical research on tegoprubart in kidney transplantation, islet cell transplantation and xenotransplantation.
    • “Eledon is currently conducting clinical research on the potential benefits of treatment with tegoprubart in kidney transplantation, islet cell transplantation and xenotransplantation.” https://eledon.com/science/pipeline/ (2026-10-19)

Target: CD40 Ligand

Keywords: xenotransplantation neurology immunology neurodegenerative diseases Kidney Transplant Rejection Prevention of Rejection in Kidney Transplant IgA Nephropathy IgAN Brittle Type 1 Diabetes Mellitus AT-1501

Location: Irvine, CA · source · Oct 15, 2026

Profile checked Oct 10, 2026

$135.0MRaised (2 yrs)6Trials (company is sponsor)

Timeline

  1. Trial start Phase 3: Study of Tegoprubart Efficacy and Safety Compared With Tacrolimus in Kidney Transplantation source ↗
  2. Raise Follow-on offering: $50M (total, as published), announced Nov 12, 2025. Source: company release on GlobeNewswire. source ↗
  3. Raise Follow-on offering: $85M (total, as published), announced Oct 29, 2024. Source: SEC filing. source ↗
  4. Trial start Phase 2: Long-Term Safety and Efficacy of Tegoprubart in Kidney Transplant Recipients source ↗
  5. Trial start Phase 2: Safety and Efficacy of Tegoprubart in Patients Undergoing Kidney Transplantation source ↗
  6. Trial start Phase 1/Phase 2: Safety, Tolerability, and Efficacy of Immunomodulation With AT-1501 in Combination With Transplanted Islet Cells in Adults With Brittle T1D source ↗
  7. Trial start Phase 2: Safety and Efficacy of AT-1501 in Patients With IgA Nephropathy (IgAN) source ↗
  8. Trial start Phase 1/Phase 2: Safety, Pharmacokinetics, and Efficacy of AT 1501 in Patients Undergoing Kidney Transplant source ↗

Upcoming milestones

Estimated primary completion per ClinicalTrials.gov. Dates move.

Funding

Raised: $135.0M. Last 2 years.

Clinical trials (lead sponsor) 6

RecordTitlePhaseStatusStartPrimary completion
NCT07835581Study of Tegoprubart Efficacy and Safety Compared With Tacrolimus in Kidney TransplantationPhase 3Not yet recruiting2026-102029-03 (estimated)
NCT05983770Safety and Efficacy of Tegoprubart in Patients Undergoing Kidney TransplantationPhase 2CompletedAug 30, 2023Sep 11, 2025 (actual)
NCT06126380Long-Term Safety and Efficacy of Tegoprubart in Kidney Transplant RecipientsPhase 2Enrolling by invitationOct 25, 20232029-12 (estimated)
NCT05027906Safety, Pharmacokinetics, and Efficacy of AT 1501 in Patients Undergoing Kidney TransplantPhase 1/Phase 2RecruitingFeb 18, 20222027-01 (estimated)
NCT05125068Safety and Efficacy of AT-1501 in Patients With IgA Nephropathy (IgAN)Phase 2TerminatedMar 21, 2022Jul 31, 2023 (actual)
NCT05480657Safety, Tolerability, and Efficacy of Immunomodulation With AT-1501 in Combination With Transplanted Islet Cells in Adults With Brittle T1DPhase 1/Phase 2WithdrawnSep 30, 20222024-08 (estimated)
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