Study in End-stage Renal Disease Patients Awaiting Kidney Transplant to Investigate the Potential Effect of IVIG Treatment on the Pharmacokinetics and Pharmacodynamics of LFG316

Completed · Phase 1

Conditions studied: Kidney Transplantation

In brief

Investigate whether concomitant treatment with intravenous immunoglobulin (IVIG) can alter the pharmacokinetics and pharmacodynamics of LFG316 to an extent which would necessitate dose adaptation for LFG316 in pre-sensitized end-stage renal disease patients awaiting kidney transplantation

Key facts

Study ID

NCT02878616

Run by

Novartis Pharmaceuticals

People needed

8

Starts

2016-08-26

Expected to finish

2017-07-19

Last updated by the study team

2020-12-11

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult men or women 18-70 years of age suffering from end-stage renal disease and who are on chronic dialysis therapy.
• Candidates for kidney transplantation who are pre-sensitized and will be undergoing desensitization therapy.
• Written informed consent must be obtained before any assessment is performed.
• Able to communicate well with the investigator, to understand and comply with the requirements of the study.
• Recipients who are ABO compatible with donor allograft.
• Patients awaiting kidney allograft from a living or deceased donor. For patients awaiting transplant from a living donor, kidney transplantation must only occur after 28 days post-LFG316 infusion.
• History of vaccination with meningococcus and pneumococcus between 2 weeks and 36 months prior to dosing. Documentation is required. If patients have not been vaccinated, they must be vaccinated at least 2 weeks prior to dosing. The choice of vaccine(s) should take into account the serotypes prevalent in the geographic areas in which study patients will be enrolled.

You may not qualify if…

• Patients requiring or undergoing peritoneal dialysis.
• Patients with a known contraindication to treatment with blood products.
• Patients with a known pro-thrombotic disorder and/or history of thrombosis or hyper-coagulable state, excluding hemodialysis venous access clotting.
• Patients who have positive PCR results for hepatitis B and/or hepatitis C, and/or history of immunodeficiency diseases, including a positive HIV (ELISA and Western blot) test result.
• Patients at risk for tuberculosis (TB)
• Patients with any severe, progressive or uncontrolled acute or chronic medical condition not related to end-stage renal disease (such as uncontrolled infectious disease or sepsis), clinical laboratory abnormalities at screening or baseline that in the investigator's opinion would make the patient inappropriate for entry into this study, or known active presence of malignancies.
• Pregnant or nursing (lactating) women.
• Women of child-bearing potential, unless highly effective methods of contraception are used during dosing and for 50 days after the last dose of LFG316, or sexually active males unwilling to use a condom during intercourse while taking investigational drug and for 50 days after the last dose of LFG316.
• Other protocol-defined inclusion/exclusion criteria may apply.

Where it is running

• Novartis Investigative Site — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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