We pursue these high-value targets using our differentiated product engine. 8226;Establish clinical proof of concept for our CDK9 program. The FDA cleared our IND for KB-0742 in December 2020. ENTO has also been tested in a Phase 1b/2 clinical trial in 148 AML patients. Dysregulation of the androgen receptor (AR) TRN is a primary driver of prostate cancer. In addition, a product may be eligible for accelerated approval. PMA applications are subject to an application fee. We are not currently a party to any material legal proceedings. Our corporate website address is www.kronosbio.com. We had cash, cash equivalents, and investments of $462.1 million as of December 31, 2020. A failure of one or more clinical trials can occur at any stage of testing. As a result, the coverage determination process is often time-consuming and costly. The development and commercialization of pharmaceutical products is highly competitive. We generally contract with third parties for the disposal of these materials and wastes. We may fail to obtain any of these licenses on commercially reasonable terms, if at all. In addition, there is a natural transition period when a new CRO commences work. We expect to rely on third parties for the manufacture of our product candidates. As of January 1, 2021, we had 63 full-time employees. Therefore, these provisions could adversely affect the price of our common stock. However, we have not opted out of this provision.