SBIR-STTR Award

Novel Assay to Monitor Tacrolimus Levels At the Point of Care
Award last edited on: 9/21/2022

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$2,528,453
Award Phase
2
Solicitation Topic Code
855
Principal Investigator
Martyn Darby

Company Information

Affinergy LLC (AKA: Affinergy Inc)

601 Keystone Park Drive Suite 100
Morrisville, NC 27560
   (919) 433-2200
   contact1@affinergy.com
   www.affinergy.com
Location: Single
Congr. District: 04
County: Wake

Phase I

Contract Number: 1R44AI140931-01
Start Date: 6/15/2018    Completed: 5/31/2019
Phase I year
2018
Phase I Amount
$300,000
In 2016, over 33,000 organ transplants were performed in the United States, an increase of 20% over the past 5 years. Organ transplantation requires lifelong immunosuppression to prevent rejection of the transplant. Tacrolimus, a macrolide antibiotic, is one of the most effective immunosuppressants, with >90% of solid organ transplant recipients receiving it as part of their maintenance immunosuppression. Tacrolimus has a narrow therapeutic window, with sub-therapeutic levels putting patients at risk for rejection and supra-therapeutic levels leading to toxicity. In addition to significant pharmacokinetic variability, it is also estimated that >25% of patients are non-adherent to their immunosuppressant regimen, significantly increasing graft rejection and failure rates and increasing the financial burden on the US healthcare system. Because transplant recipients require a lifetime of immunosuppression, any methods that facilitate improved dosing and rapid detection of non-adherence are of great clinical utility. Because tacrolimus levels cannot be ascertained at the point of care, detection of non-therapeutic levels in the outpatient setting is challenging. Patients must either attend a separate lab appointment ahead of their routine follow-up visits or they have levels drawn on the day of their visit. In the former, an extra burden is placed on the patient to attend an additional appointment while the latter precludes analysis of levels prior to the patientÂ’s appointment. Delays in medication management or identification of patient non-compliance place the patient at risk for graft rejection (sub-therapeutic levels) or drug-associated toxicities (supra-therapeutic levels). To address this technical hurdle, Affinergy plans to develop a point-of-care lateral flow assay that will enable frequent, accurate and affordable monitoring of tacrolimus levels. We have already generated a proprietary capture reagent and identified several detection reagent candidates that bind with nanomolar affinity to tacrolimus. At the conclusion of Phase I, we will have a prototype lateral flow assay with established limits of quantitation. In Phase II, we will scale up production of our assay, optimize performance characteristics, establish storage conditions, determine stability and evaluate our assay using transplant recipient blood specimens. Successful completion of this project will lead to improved long-term maintenance of patients receiving tacrolimus for immunosuppression and ease the burden on both patients and providers.

Public Health Relevance Statement:
PROJECT NARRATIVE Tacrolimus concentration must be closely monitored in transplant recipients as a part of their lifelong immunosuppression. However, patients receiving tacrolimus in the outpatient setting must have blood levels shipped out or drawn the day of their visit, leading to unacceptable delays in dosage adjustment. In this Fast- Track application, we propose to develop a novel peptide-based sandwich assay to facilitate rapid, affordable, point-of-care measurement of tacrolimus concentration in biological fluids.

Project Terms:
Address; Affinity; Appointment; base; Binding; Biological; Biological Assay; Blood; Blood specimen; Characteristics; Clinic; Clinical; Complex; cross reactivity; design; Detection; Development; dosage; Dose; Drug Kinetics; Early identification; Evaluation; follow-up; Freezing; graft failure; Graft Rejection; Guidelines; Healthcare; Healthcare Systems; Immunosuppression; Immunosuppressive Agents; improved; Institutes; Label; Laboratories; large scale production; Lateral; Libraries; Life; Liquid substance; lot production; Macrolide Antibiotics; Maintenance; Measurement; Measures; Medication Management; Methodology; Methods; Monitor; nanomolar; novel; Organ Transplantation; Outpatients; particle; Patient Appointment; Patient Noncompliance; Patients; Peptides; Performance; performance tests; Pharmaceutical Preparations; Phase; point of care; prevent; Production; prototype; Provider; rapid detection; Reader; Reagent; receptor; Regimen; Reproducibility; Risk; Running; Sampling; scale up; Ships; Solid; Specificity; Specimen; stability testing; Tacrolimus; Tacrolimus Binding Proteins; Testing; Therapeutic; Toxic effect; Transplant Recipients; United States; Validation; verification and validation; Visit; Whole Blood

Phase II

Contract Number: 4R44AI140931-02
Start Date: 6/15/2018    Completed: 7/31/2022
Phase II year
2019
(last award dollars: 2021)
Phase II Amount
$2,228,453

In 2016, over 33,000 organ transplants were performed in the United States, an increase of 20% over the past 5 years. Organ transplantation requires lifelong immunosuppression to prevent rejection of the transplant. Tacrolimus, a macrolide antibiotic, is one of the most effective immunosuppressants, with >90% of solid organ transplant recipients receiving it as part of their maintenance immunosuppression. Tacrolimus has a narrow therapeutic window, with sub-therapeutic levels putting patients at risk for rejection and supra-therapeutic levels leading to toxicity. In addition to significant pharmacokinetic variability, it is also estimated that >25% of patients are non-adherent to their immunosuppressant regimen, significantly increasing graft rejection and failure rates and increasing the financial burden on the US healthcare system. Because transplant recipients require a lifetime of immunosuppression, any methods that facilitate improved dosing and rapid detection of non-adherence are of great clinical utility. Because tacrolimus levels cannot be ascertained at the point of care, detection of non-therapeutic levels in the outpatient setting is challenging. Patients must either attend a separate lab appointment ahead of their routine follow-up visits or they have levels drawn on the day of their visit. In the former, an extra burden is placed on the patient to attend an additional appointment while the latter precludes analysis of levels prior to the patientÂ’s appointment. Delays in medication management or identification of patient non-compliance place the patient at risk for graft rejection (sub-therapeutic levels) or drug-associated toxicities (supra-therapeutic levels). To address this technical hurdle, Affinergy plans to develop a point-of-care lateral flow assay that will enable frequent, accurate and affordable monitoring of tacrolimus levels. We have already generated a proprietary capture reagent and identified several detection reagent candidates that bind with nanomolar affinity to tacrolimus. At the conclusion of Phase I, we will have a prototype lateral flow assay with established limits of quantitation. In Phase II, we will scale up production of our assay, optimize performance characteristics, establish storage conditions, determine stability and evaluate our assay using transplant recipient blood specimens. Successful completion of this project will lead to improved long-term maintenance of patients receiving tacrolimus for immunosuppression and ease the burden on both patients and providers.

Public Health Relevance Statement:
PROJECT NARRATIVE Tacrolimus concentration must be closely monitored in transplant recipients as a part of their lifelong immunosuppression. However, patients receiving tacrolimus in the outpatient setting must have blood levels shipped out or drawn the day of their visit, leading to unacceptable delays in dosage adjustment. In this Fast- Track application, we propose to develop a novel peptide-based sandwich assay to facilitate rapid, affordable, point-of-care measurement of tacrolimus concentration in biological fluids.

Project Terms:
Address; Affinity; Appointment; base; Binding; Biological; Biological Assay; Blood; Blood specimen; Characteristics; Clinic; Clinical; Complex; cross reactivity; design; Detection; Development; dosage; Dose; Drug Kinetics; Early identification; Evaluation; Financial Hardship; follow-up; Freezing; graft failure; Graft Rejection; Guidelines; Healthcare Systems; Immunosuppression; Immunosuppressive Agents; improved; Institutes; Label; Laboratories; large scale production; Lateral; Libraries; Life; Liquid substance; lot production; Macrolide Antibiotics; Maintenance; Measurement; Measures; Medication Management; Methodology; Methods; Monitor; nanomolar; novel; Organ Transplantation; Outpatients; Patient Appointment; Patient Noncompliance; Patients; Peptides; Performance; performance tests; Pharmaceutical Preparations; Phase; point of care; prevent; Production; prototype; Provider; rapid detection; Reader; Reagent; receptor; Regimen; Reproducibility; Risk; Running; Sampling; scale up; Ships; Solid; Specificity; Specimen; stability testing; Tacrolimus; Tacrolimus Binding Proteins; Testing; Therapeutic; Toxic effect; Transplant Recipients; United States; Validation; verification and validation; Visit; Whole Blood