A Phase II Study to Evaluate the Efficacy of IdeS to Desensitize Transplant Patients With a Positive Crossmatch Test

Completed · Phase 2

Conditions studied: Kidney Failure, Chronic

In brief

The purpose of this study is to evaluate the effectiveness of the study drug IdeS in patients who are on the waiting list for kidney transplant and have previously undergone desensitization unsuccessfully or in whom effective desensitization will be highly unlikely. At study entry, the patients will have an available deceased or live donor with a positive crossmatch test. The study will assess IdeS efficacy and safety in removing Donor Specific Antibodies (DSAs) and thereby convert a positive crossmatch test to negative.

Key facts

Study ID

NCT02790437

Run by

Hansa Biopharma AB

People needed

19

Starts

2016-06-01

Expected to finish

2018-07-03

Last updated by the study team

2021-05-20

Who can join

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

You may qualify if…

• Patients on the kidney transplant waitlist who have previously undergone desensitization unsuccessfully or in whom effective desensitization will be highly unlikely. The breadth and strength of sensitization will predict an extremely low likelihood of successful desensitization or kidney paired donation.
• Patients with a live or deceased donor with a positive crossmatch test.

You may not qualify if…

• Previous treatment with IdeS
• Previous high dose IVIg treatment (2 g/kg BW) within 28 days prior to IdeS treatment
• Lactating or pregnant females
• Women of child-bearing age who are not willing or able to practice FDA-approved forms of contraception
• HIV-positive patients
• Patients with clinical signs of HBV or HCV infection
• Patients with active tuberculosis
• A significantly abnormal general serum screening lab result according to the investigator's judgement. Hgb cannot be < 6.0 g/dL
• Severe other conditions requiring treatment and close monitoring, e.g. cardiac failure > NYHA (New York Heart Association) grade 3, unstable coronary disease or oxygen dependent COPD
• Individuals deemed unable to comply with the protocol
• Patients with clinical signs of CMV or EBV infection
• Patients with a history of major thrombotic events, patients with active peripheral vascular disease or patients with proven hypercoagulable conditions
• Patients should not have received investigational drugs within 4 half-lives (or similar)
• Known allergy/sensitivity to IdeS infusions
• Patients who have a live donor and test positive for ImmunoCap anti-IdeS IgE

Where it is running

• Cedars-Sinai Medical Center — Los Angeles, California, United States
• The Johns Hopkins Hospital — Baltimore, Maryland, United States
• New York University School of Medicine — New York, New York, United States
• Necker Hospital — Paris, France
• Uppsala University Hospital — Uppsala, Sweden

Full record on ClinicalTrials.gov

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