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Search / Trial NCT06126380

Long-Term Safety and Efficacy of Tegoprubart in Kidney Transplant Recipients

Launched by ELEDON PHARMACEUTICALS · Nov 6, 2023

Trial Information

Current as of June 26, 2025

Enrolling by invitation

Keywords

Kidney Transplant At 1501 Renal Allograft Rejection Prophylaxis Cd40 L Inhibitor Humanized Blocking Antibody To Cd40 L Monoclonal Antibody Renal, Transplant Esrd Tegoprubart

ClinConnect Summary

This is a multicenter, open-label, active control extension study to assess the long-term safety and efficacy of AT-1501 (tegoprubart) compared with tacrolimus in the preservation of allograft function after kidney transplantation.

The number of patients enrolled for OLE study will depend on the enrollment in the Parent studies. To be eligible for participation in this study, participants must have completed a designated Parent study.

Participants in this study will continue the treatment regimen they were receiving in the Parent study. Dose regimens will include either AT-1501 (tegopruba...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Successfully completed qualifying Parent study, where entry into the OLE was offered;
  • Continue to be able to understand the key components of the study as described in the written ICF, and is willing and able to provide written informed consent;
  • Agree not to participate in another interventional study while on treatment;
  • If female, is surgically sterile or 2 years postmenopausal. Women of childbearing potential may be enrolled if a pregnancy test is negative at baseline. Women of childbearing potential and men with partners that are of childbearing potential must agree to use highly effective methods of contraception from baseline, through 90 days after the last administration of the study drug. Examples of acceptable methods of contraception are described in Table 6.
  • If male, agree to use a medically accepted highly effective method of contraception and agree to use this method for 90 days after last administration of the study drug and agree to not donate sperm for 90 days after last administration of the study drug.
  • Exclusion Criteria:
  • Unwilling or unlikely to comply with the study requirements, in the opinion of the Investigator;
  • Met any of the stopping criteria or discontinued study drug in the Parent study;
  • Pregnant or breastfeeding.

About Eledon Pharmaceuticals

Eledon Pharmaceuticals is a biopharmaceutical company focused on developing innovative therapies for severe autoimmune and neurodegenerative diseases. With a commitment to advancing patient care, Eledon leverages cutting-edge science and technology to create targeted treatments that address unmet medical needs. The company's pipeline includes novel drug candidates designed to modulate the immune system and promote neuroprotection, underscoring its dedication to improving the quality of life for patients suffering from debilitating conditions. Through rigorous clinical trials and a collaborative approach, Eledon Pharmaceuticals aims to bring transformative solutions to market, fostering hope and resilience in the communities it serves.

Locations

Rochester, Minnesota, United States

Kansas City, Kansas, United States

Durham, North Carolina, United States

Maywood, Illinois, United States

Adelaide, South Australia, Australia

Detroit, Michigan, United States

Washington, District Of Columbia, United States

Saint Louis, Missouri, United States

Richmond, Virginia, United States

Atlanta, Georgia, United States

Los Angeles, California, United States

Cincinnati, Ohio, United States

Barcelona, , Spain

St. Louis, Missouri, United States

Barcelona, , Spain

Barcelona, , Spain

Baltimore, Maryland, United States

Dallas, Texas, United States

Berlin, , Germany

Bordeaux, , France

Los Angeles, California, United States

Barcelona, , Spain

Montréal, Quebec, Canada

Oxford, , United Kingdom

Harrisburg, Pennsylvania, United States

Vancouver, British Columbia, Canada

Grenoble, , France

Toulouse, , France

São Paulo, , Brazil

São Paulo, , Brazil

Limoges, , France

Barcelona, , Spain

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported