Tasca launches to drug protein pockets

Tasca Therapeutics has launched to develop small molecules designed to bind to proteins with hydrophobic pockets that undergo autopalmitoylation, a process that determines where the protein goes and what it does. The start-up has raised $52 million across a seed and series A round. Cure Ventures co-led the series A with the venture arm of Regeneron. Tasca will start by evaluating its lead drug candidate—a molecule called CP-383—in small-cell lung cancer, colorectal cancer, head and neck cancer, and glioblastoma. CEO Milenko Cicmil says the last indication is of particular interest because CP-383 can cross the blood-brain barrier—a challenge in treating the infamously aggressive brain cancer.

Authors

Publication Details

Journal
C&EN Global Enterprise
Published
2024-12-20
DOI
https://doi.org/10.1021/cen-10239-buscon16
Primary Topic
Biotechnology and Related Fields
Type
article
Field-Weighted Citation Impact
0.00
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article

Tasca launches to drug protein pockets

Rowan Walrath
C&EN Global Enterprise
Biotechnology and Related Fields
article

Tasca launches to drug protein pockets

Rowan Walrath
article en

Abstract

Tasca Therapeutics has launched to develop small molecules designed to bind to proteins with hydrophobic pockets that undergo autopalmitoylation, a process that determines where the protein goes and what it does. The start-up has raised $52 million across a seed and series A round. Cure Ventures co-led the series A with the venture arm of Regeneron. Tasca will start by evaluating its lead drug candidate—a molecule called CP-383—in small-cell lung cancer, colorectal cancer, head and neck cancer, and glioblastoma. CEO Milenko Cicmil says the last indication is of particular interest because CP-383 can cross the blood-brain barrier—a challenge in treating the infamously aggressive brain cancer.

C&EN Global EnterpriseVol. 102(39)
Openalex Percentile: Top 64%
Biotechnology and Related Fields
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Tasca launches to drug protein pockets — Rowan Walrath · C&EN Global Enterprise (2024) | TGRS Research Map | TGRS