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ALD1613, A Novel Long-Acting Monoclonal Antibody to Control ACTH-Driven Pharmacology
Author(s) -
Andrew L. Feldhaus,
Katie L. Anderson,
Benjamin Dutzar,
Ethan W. Ojala,
Patricia D. McNeill,
Pei Fan,
Jenny Mulligan,
Sam Marzolf,
Charlie Karasek,
Michelle ScalleyKim,
Erica Stewart,
Jens Billgren,
Vanessa Rubin,
Kathleen Schneider,
David Jurchen,
Kathy J. Snow,
Shaun Barnett,
Barbara Bengtsson,
Brian Baker,
John Latham,
Dan Allison,
León F. Garcı́a-Martı́nez
Publication year - 2016
Publication title -
endocrinology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2016-1455
Subject(s) - medicine , endocrinology , adrenocorticotropic hormone , acth receptor , corticosterone , monoclonal antibody , cyclic adenosine monophosphate , glucocorticoid , adrenal gland , monoclonal , receptor , antibody , hormone , biology , immunology
Adrenocorticotropic hormone (ACTH) is the primary regulator of adrenal glucocorticoid production. Elevated levels of ACTH play a critical role in disease progression in several indications, including congenital adrenal hyperplasia and Cushing disease. We have generated a specific, high-affinity, neutralizing monoclonal antibody (ALD1613) to ACTH. In vitro, ALD1613 neutralizes ACTH-induced signaling via all 5 melanocortin receptors and inhibited ACTH-induced cyclic adenosine monophosphate accumulation in a mouse adrenal cell line (Y1). ALD1613 administration to wild-type rats significantly reduced plasma corticosterone levels in a dose-dependent manner. In rodent models with either chronic infusion of ACTH or acute restraint stress-induced ACTH, corticosterone levels were significantly reduced by ALD1613. Administration of ALD1613 to nonhuman primates on days 1 and 7 stably reduced plasma cortisol levels >50% for 57 days. ALD1613 demonstrates the potential of a monoclonal antibody to be an effective therapeutic for conditions with elevated ACTH levels.

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