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.
- 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].
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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Cat. No.Product NameDescriptionTargetResearch Area
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target: Bcl-2 FamilyResearch Areas: Cancer