ALD1613, a Novel Long-Acting Monoclonal Antibody to Control ACTH-Driven Pharmacology

  • Endocrinology. 2017 Jan 1;158(1):1-8. doi: 10.1210/en.2016-1455.
Andrew L Feldhaus  1 ,  Katie Anderson  1 ,  Benjamin Dutzar  1 ,  Ethan Ojala  1 ,  Patricia Dianne McNeill  1 ,  Pei Fan  1 ,  Jenny Mulligan  1 ,  Sam Marzolf  1 ,  Charlie Karasek  1 ,  Michelle Scalley-Kim  1 ,  Erica Stewart  1 ,  Jens Billgren  1 ,  Vanessa Rubin  1 ,  Kathleen Schneider  1 ,  David Jurchen  1 ,  Kathy Snow  1 ,  Shaun Barnett  1 ,  Barbara Bengtsson  1 ,  Brian Baker  1 ,  John A Latham  1 ,  Dan Allison  1 ,  Leon F Garcia-Martinez  1
Affiliations
  • 1. Alder BioPharmaceuticals, Inc., Bothell, Washington 98011.
Abstract

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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