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Field Study and Correlative Studies of Factor IX Variant FIX-R338L in Participants Treated with Fidanacogene Elaparvovec.

Authors :
Pittman DD
Carrieri C
Soares H
McKay J
Tan CY
Liang JZ
Rakhe S
Marshall JC
Murphy JE
Gaitonde P
Rupon J
Source :
Thrombosis and haemostasis [Thromb Haemost] 2024 Oct; Vol. 124 (10), pp. 912-921. Date of Electronic Publication: 2024 Jun 11.
Publication Year :
2024

Abstract

Background:  Fidanacogene elaparvovec, an adeno-associated virus-based gene therapy vector expressing the high-activity factor IX (FIX) variant FIX-R338L, is in development for hemophilia B. One-stage clotting (OS) assays and chromogenic substrate (CS) assays are commonly used to measure FIX-R338L variant activity. Data from ongoing trials suggest FIX activity varies between different OS and CS assays.<br />Material and Methods:  To better understand FIX-R338L activity in clinical samples, an international multisite field study was conducted across a central laboratory and 18 local laboratories, using standard protocols, reagents, and instrumentation, with individual participant samples from a phase 1/2a study of fidanacogene elaparvovec.<br />Results:  Unlike the wild-type FIX control, FIX-R338L activity was higher with the OS silica-based assay versus OS ellagic acid-based and CS assays. Variation in FIX activity was greater at the lowest activity levels. Activated FIX (FIXa) in plasma could result in higher OS assay activity or increased thrombin generation, which could overestimate FIX activity. However, FIXa was not detected in the participant samples, indicating that it was not contributing to the OS assay differences. Since individuals on gene therapy may receive exogenous replacement FIX products, replacement products were spiked into patient plasma samples to target a therapeutic concentration. Exogenous FIX was additive to endogenous FIX-R338L, with no interference from FIX-R338L.<br />Conclusion:  These results demonstrate FIX-R338L activity can be measured with OS and CS assays in clinical laboratories and provide insight into assay variability when measuring FIX with endogenously produced FIX-R338L. The findings may help establish best practices for measuring FIX-R338L activity (Clinicaltrials.gov identifier: NCT02484092).<br />Competing Interests: C.C., J.M., C.Y.T., J.Z.L., P.G., and J.R. are employees of Pfizer and may own stock/options in the company. D.D.P., H.S., S.R., J.-C.M., and J.E.M. were employees of Pfizer at the time of the study conduct and may own stock/options in the company.<br /> (The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).)

Details

Language :
English
ISSN :
2567-689X
Volume :
124
Issue :
10
Database :
MEDLINE
Journal :
Thrombosis and haemostasis
Publication Type :
Academic Journal
Accession number :
38863155
Full Text :
https://doi.org/10.1055/s-0044-1787734