Back to Search Start Over

Expanding the Repertoire for "Large Small Molecules": Prodrug ABBV-167 Efficiently Converts to Venetoclax with Reduced Food Effect in Healthy Volunteers.

Authors :
Salem AH
Tao ZF
Bueno OF
Chen J
Chen S
Edalji R
Elmore SW
Fournier KM
Harper KC
Hong R
Jenkins GJ
Ji J
Judge RA
Kalvass JC
Klix RC
Ku YY
Leverson JD
Marks RA
Marsh KC
Menon RM
Park CH
Phillips DC
Pu YM
Rosenberg SH
Sanzgiri YD
Sheikh AY
Shi Y
Stolarik D
Suleiman AA
Wang X
Zhang GGZ
Catron ND
Souers AJ
Source :
Molecular cancer therapeutics [Mol Cancer Ther] 2021 Jun; Vol. 20 (6), pp. 999-1008. Date of Electronic Publication: 2021 Mar 30.
Publication Year :
2021

Abstract

Since gaining approval for the treatment of chronic lymphocytic leukemia (CLL), the BCL-2 inhibitor venetoclax has transformed the treatment of this and other blood-related cancers. Reflecting the large and hydrophobic BH3-binding groove within BCL-2, venetoclax has significantly higher molecular weight and lipophilicity than most orally administered drugs, along with negligible water solubility. Although a technology-enabled formulation successfully achieves oral absorption in humans, venetoclax tablets have limited drug loading and therefore can present a substantial pill burden for patients in high-dose indications. We therefore generated a phosphate prodrug ( 3 , ABBV-167) that confers significantly increased water solubility to venetoclax and, upon oral administration to healthy volunteers either as a solution or high drug-load immediate release tablet, extensively converts to the parent drug. Additionally, ABBV-167 demonstrated a lower food effect with respect to venetoclax tablets. These data indicate that beyond-rule-of-5 molecules can be successfully delivered to humans via a solubility-enhancing prodrug moiety to afford robust exposures of the parent drug following oral dosing.<br /> (©2021 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1538-8514
Volume :
20
Issue :
6
Database :
MEDLINE
Journal :
Molecular cancer therapeutics
Publication Type :
Academic Journal
Accession number :
33785651
Full Text :
https://doi.org/10.1158/1535-7163.MCT-21-0077