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

  • Mol Cancer Ther. 2021 Jun;20(6):999-1008. doi: 10.1158/1535-7163.MCT-21-0077.
Ahmed Hamed Salem  1  2 Zhi-Fu Tao  1 Orlando F Bueno  1 Jie Chen  1 Shuang Chen  1 Rohinton Edalji  1 Steven W Elmore  1 Keith M Fournier  1 Kaid C Harper  1 Richard Hong  1 Gary J Jenkins  1 Jianguo Ji  1 Russell A Judge  1 John C Kalvass  1 Russell C Klix  1 Yi-Yin Ku  1 Joel D Leverson  1 Richard A Marks  1 Kennan C Marsh  1 Rajeev M Menon  1 Chang H Park  1 Darren C Phillips  1 Yu-Ming Pu  1 Saul H Rosenberg  1 Yeshwant D Sanzgiri  1 Ahmad Y Sheikh  1 Yi Shi  1 Deanne Stolarik  1 Ahmed A Suleiman  3 Xilu Wang  1 Geoff G Z Zhang  1 Nathaniel D Catron  1 Andrew J Souers  4
Affiliations
  • 1. AbbVie, Inc., North Chicago, Illinois.
  • 2. Ain Shams University, Cairo, Egypt.
  • 3. AbbVie Deutschland GmbH & Co. KG, Ludwigshafen am Rhein, Germany.
  • 4. AbbVie, Inc., North Chicago, Illinois. [email protected].
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.

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