Graft Acute Kidney Injury: Vitamin B3 to Facilitate Renal Recovery In the Early Life of a Transplant (GABRIEL)
Primary Purpose
Delayed Graft Function
Status
Not yet recruiting
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Nicotinamide treatment
Placebo treatment
Sponsored by
About this trial
This is an interventional treatment trial for Delayed Graft Function focused on measuring Kidney Transplantation, Delayed Graft Function, Niacinamide, Acute Kidney Injury, Acute Tubular Necrosis, creatinine reduction ratio, Nicotinamide Adenine Dinucleotide, Quinolinate, urinary quinolinate / tryptophane
Eligibility Criteria
Inclusion Criteria:
- Age ≥18 years,
- Patients in end stage renal disease (ESRD) requiring dialysis (hemodialysis or peritoneal dialysis),
- Kidney transplant with deceased donor (brain death or cardiac death Maastricht 3),
- Affiliation to French social security ("AME" excepted),
- Written informed consent
Exclusion Criteria:
- Preemptive transplant,
- Pregnancy,
- Liver disease defined by the necessity for a specialized follow-up by an hepatologist or by elevated liver enzymes > 3N (ALAT, gammaGT) on the day of transplantation,
- Transplantation of multiple organs,
- Hypersensitivity to nicotinamide or one of excipients,
- Participation to another interventional study (RIPH1),
- Patient under legal protection measure (tutorship or curatorship) and patient deprived of freedom.
Sites / Locations
- Department of Renal Transplantation - Hospital Pitié Salpétrière
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Nicotinamide
Placebo
Arm Description
Outcomes
Primary Outcome Measures
Efficacy of 3 doses of NAM given orally at 1g/dose immediately pre transplant and during the first 2 post-operative days of renal transplantation versus placebo, on the early graft function, assessed by CRR2.
The primary endpoint is based on creatinine reduction ratio between days 1 and 2 (CRR2, calculated by the following formula: CRR2 (%) = ([Cr1-Cr2]×100)/Cr1, where Cr1 and Cr2 are the morning serum creatinine on post-operative day 1 and day 2 respectively.
Secondary Outcome Measures
Verify the safety profile of NAM (liver toxicity and tacrolimus trough levels to detect an interaction)
Proportion of patients with at least one increase of ALAT concentrations > 2N between V0 and POD7 (mild and reversible liver toxicity has been described with high dose NAM treatment ; and proportion of patients with inadequately high tacrolimus trough levels (> 15 ng/mL) at POD2, and POD7.
Evaluate the effect of NAM on the rate of delayed graft function defined conventionally as the need for dialysis before POD7
Rate of DGF (Delayed Graft Function), as defined by the need of at least one dialysis between engraftment and POD7
Evaluate the effect of NAM on renal graft function 3 months after transplantation
Correlation between CRR2 and :
eGFR 3 months after transplantation among patients with no renal event such as, rejection, pyelonephritis and obstruction.
Urinary quinolinate/tryptophan ratio measured by mass spectrometry at 3 months after transplantation among patients with no renal event such as, rejection, pyelonephritis and obstruction
Evaluate the effect of NAM on serum NAM levels (difference between NAM at POD2 and NAM at baseline)
Comparison of NAM concentration variation from baseline to POD2.
Evaluate the effect of NAM on the biopsy-proven rejection rate within three months after transplantation.
Proportion of patients with at least one episode of biopsy-proven rejection (T-cell or antibody mediated) as per the Banff's 2017 classification criteria (48) within 3 months after transplantation
Measurement accuracy, and positive predictive value of the urinary quinolinate / tryptophane ratio measured early after transplantation (at POD2) for CRR2, DGF, and graft function estimated by MDRD at 3 months
Urinary quinolinate/tryptophan ratio measured by mass spectrometry at POD2 where we expect an increase in patients with DGF and also at M3, to determine the reversibility of the metabolic abnormalities.
Evaluate the effect of NAM serum concentration at baseline on the level of risk of DGF
Serum concentration of NAM at baseline (before pre transplant NAM dose), measured by mass spectrometry
Cost-effectiveness and cost utility of NAM after transplantation of a kidney from a deceased donor
Incremental cost effectiveness ratio of NAM compared to placebo, measured by the difference in costs of healthcare divided by the difference in rate of 3-month renal events defined as rejection, pyelonephritis and obstruction and incremental cost utility analysis using quality adjusted life years
Comparison of different separation techniques (LC, HILIC, IC, EC) for MS quantification of uQ/T and serum NAM
Reproductibility of the quantification of urinary quinolinate/tryptophan ratio and serum concentration of NAM, measured by mass spectrometry
Full Information
NCT ID
NCT05513807
First Posted
August 22, 2022
Last Updated
October 17, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, Centre National de la Recherche Scientifique, France
1. Study Identification
Unique Protocol Identification Number
NCT05513807
Brief Title
Graft Acute Kidney Injury: Vitamin B3 to Facilitate Renal Recovery In the Early Life of a Transplant
Acronym
GABRIEL
Official Title
Graft Acute Kidney Injury: Vitamin B3 to Facilitate Renal Recovery In the Early Life of a Transplant - GABRIEL
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 2022 (Anticipated)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
November 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, Centre National de la Recherche Scientifique, France
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Delayed graft function occurs in more than 20% of kidney transplantations. It is an episode of post-ischemic acute kidney injury with long-term consequences on the allograft's function. Based on preclinical data and on a stage 1 clinical trial, the hypothesize is that an acquired defect in NAD+ biosynthesis is instrumental in delayed graft function and that a treatment with high doses of vitamin B3 (nicotinamide) will improve the early renal graft function.
Thus, it is planned to recruit 204 kidney allograft recipients immediately before transplantation and randomize them to either placebo or nicotinamide treatment for 3 administrations before transplantation, immediately after it and on the next day.
The efficacy of nicotinamide to foster early graft function will be evaluated by comparing the creatinine reduction ratio between the placebo and the nicotinamide treated groups.
Serum will be collected before and 2 days after transplantation and urine 2 days and 3 months after transplantation to study the relationship between biological markers of NAD+ biosynthesis and nicotinamide's effect on early kidney graft function.
Detailed Description
Delayed graft function (DGF) is a frequent event in kidney transplantation (nationwide, 20.9% if all kinds of donors are included), and is prejudicial to graft survival. DGF is mostly due to acute tubular necrosis (ATN), induced by different cycles of renal ischemia (cold and warm). Until now, ATN has no specific treatment. Nicotinamide (NAM), also known as vitamin PP or as a vitamin B3 analog has recently emerged as a major therapeutic option to prevent ATN and accelerate its recovery. NAM actually allows maintaining mitochondrial function in the context of renal ischemia. In humans, NAM given orally (1 and 3g/day for 3 days) was shown to be effective in a phase I study and was associated with a 35% decreased incidence of AKI in 41 high-risk cardiac surgery patients. It has a well-known and highly favorable safety profile.
The GABRIEL study aims at testing its beneficial properties in the specific context of DGF in phase III study. The early kidney allograft function will be assessed on the creatinine reduction ratio between days 1 and 2 (CRR2, calculated by the following formula: CRR2 (%) = ([Cr1-Cr2]×100)/Cr1, where Cr1 and Cr2 are the morning serum creatinine on post-operative day 1 and day 2 respectively.
The objectives are also to :
Verify the safety profile of NAM (liver toxicity and tacrolimus trough levels to detect an interaction)
Evaluate the effect of NAM on the rate of delayed graft function defined conventionally as the need for dialysis before POD7.
Evaluate the effect of NAM on renal graft function 3 months after transplantation.
Evaluate the effect of NAM on serum NAM levels (difference between NAM at POD2 and NAM at baseline)
Evaluate the effect of NAM on the biopsy-proven rejection rate within three months after transplantation.
Measurement accuracy, and positive predictive value of the urinary quinolinate / tryptophane ratio measured early after transplantation (at POD2) for CRR2, DGF, and graft function estimated by MDRD at 3 months.
Evaluate the effect of NAM serum concentration at baseline on the level of risk of DGF.
Cost-effectiveness of NAM after transplantation of a kidney from a deceased donor.
Comparison of different separation techniques (LC, HILIC, IC, EC) for MS quantification of uQ/T and serum NAM.
Patients called for transplantation will be included if they meet the required criteria. After inclusion and according to randomization, the patient will receive the first dose of treatment (1g NAM or placebo, V0) immediately before surgery, at the time of induction of immunosuppression. The second dose will be given to the patient immediately after recovery room (POD1), and the third dose 24 hours thereafter (POD2). NAM administrations will be no less than 8 and no more than 26 hours apart. The biological samples and anamnestic items will be collected between 6 and 10 AM on the prespecified visits.
A quality of life questionnaire EQ5D will be completed by the patient at V0 after inclusion and before transplantation ; and others EQ5D questionnaires will be completed at POD7 and last study visit M3.
It is expected that this study will inform on the effect of NAM on early graft function, and help to define its potential place in the management of a subset if not all kidney transplant patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delayed Graft Function
Keywords
Kidney Transplantation, Delayed Graft Function, Niacinamide, Acute Kidney Injury, Acute Tubular Necrosis, creatinine reduction ratio, Nicotinamide Adenine Dinucleotide, Quinolinate, urinary quinolinate / tryptophane
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
204 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Nicotinamide
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Nicotinamide treatment
Other Intervention Name(s)
NICOBION
Intervention Description
3g Nicotinamide orally (1g immediately pre transplant, then 1g post-transplant in the recovery room and 1g 24 hours later)
Intervention Type
Drug
Intervention Name(s)
Placebo treatment
Intervention Description
3g Placebo orally (1g immediately pre transplant, then 1g post-transplant in the recovery room and 1g 24 hours later)
Primary Outcome Measure Information:
Title
Efficacy of 3 doses of NAM given orally at 1g/dose immediately pre transplant and during the first 2 post-operative days of renal transplantation versus placebo, on the early graft function, assessed by CRR2.
Description
The primary endpoint is based on creatinine reduction ratio between days 1 and 2 (CRR2, calculated by the following formula: CRR2 (%) = ([Cr1-Cr2]×100)/Cr1, where Cr1 and Cr2 are the morning serum creatinine on post-operative day 1 and day 2 respectively.
Time Frame
Post-Operative Day 2
Secondary Outcome Measure Information:
Title
Verify the safety profile of NAM (liver toxicity and tacrolimus trough levels to detect an interaction)
Description
Proportion of patients with at least one increase of ALAT concentrations > 2N between V0 and POD7 (mild and reversible liver toxicity has been described with high dose NAM treatment ; and proportion of patients with inadequately high tacrolimus trough levels (> 15 ng/mL) at POD2, and POD7.
Time Frame
Post-Operative Day 7
Title
Evaluate the effect of NAM on the rate of delayed graft function defined conventionally as the need for dialysis before POD7
Description
Rate of DGF (Delayed Graft Function), as defined by the need of at least one dialysis between engraftment and POD7
Time Frame
Post-Operative Day 7
Title
Evaluate the effect of NAM on renal graft function 3 months after transplantation
Description
Correlation between CRR2 and :
eGFR 3 months after transplantation among patients with no renal event such as, rejection, pyelonephritis and obstruction.
Urinary quinolinate/tryptophan ratio measured by mass spectrometry at 3 months after transplantation among patients with no renal event such as, rejection, pyelonephritis and obstruction
Time Frame
3 months after transplantation
Title
Evaluate the effect of NAM on serum NAM levels (difference between NAM at POD2 and NAM at baseline)
Description
Comparison of NAM concentration variation from baseline to POD2.
Time Frame
Post-Operative Day 2
Title
Evaluate the effect of NAM on the biopsy-proven rejection rate within three months after transplantation.
Description
Proportion of patients with at least one episode of biopsy-proven rejection (T-cell or antibody mediated) as per the Banff's 2017 classification criteria (48) within 3 months after transplantation
Time Frame
3 months after transplantation
Title
Measurement accuracy, and positive predictive value of the urinary quinolinate / tryptophane ratio measured early after transplantation (at POD2) for CRR2, DGF, and graft function estimated by MDRD at 3 months
Description
Urinary quinolinate/tryptophan ratio measured by mass spectrometry at POD2 where we expect an increase in patients with DGF and also at M3, to determine the reversibility of the metabolic abnormalities.
Time Frame
Post-operative Day 2
Title
Evaluate the effect of NAM serum concentration at baseline on the level of risk of DGF
Description
Serum concentration of NAM at baseline (before pre transplant NAM dose), measured by mass spectrometry
Time Frame
3 months after transplantation
Title
Cost-effectiveness and cost utility of NAM after transplantation of a kidney from a deceased donor
Description
Incremental cost effectiveness ratio of NAM compared to placebo, measured by the difference in costs of healthcare divided by the difference in rate of 3-month renal events defined as rejection, pyelonephritis and obstruction and incremental cost utility analysis using quality adjusted life years
Time Frame
Baseline
Title
Comparison of different separation techniques (LC, HILIC, IC, EC) for MS quantification of uQ/T and serum NAM
Description
Reproductibility of the quantification of urinary quinolinate/tryptophan ratio and serum concentration of NAM, measured by mass spectrometry
Time Frame
3 months after transplantation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥18 years,
Patients in end stage renal disease (ESRD) requiring dialysis (hemodialysis or peritoneal dialysis),
Kidney transplant with deceased donor (brain death or cardiac death Maastricht 3),
Affiliation to French social security ("AME" excepted),
Written informed consent
Exclusion Criteria:
Preemptive transplant,
Pregnancy,
Liver disease defined by the necessity for a specialized follow-up by an hepatologist or by elevated liver enzymes > 3N (ALAT, gammaGT) on the day of transplantation,
Transplantation of multiple organs,
Hypersensitivity to nicotinamide or one of excipients,
Participation to another interventional study (RIPH1),
Patient under legal protection measure (tutorship or curatorship) and patient deprived of freedom.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pierre GALICHON, Doctor
Phone
0142177201
Email
pierre.galichon@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Alexandre HERTIG, Professor
Phone
0146251020
Email
a.hertig@hopital-foch.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pierre GALICHON, Doctor
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Renal Transplantation - Hospital Pitié Salpétrière
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre GALICHON, Md, PhD
Phone
0142177229
Email
pierre.galichon@aphp.fr
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Graft Acute Kidney Injury: Vitamin B3 to Facilitate Renal Recovery In the Early Life of a Transplant
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