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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported