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On September 7, the CDE official website showed that AstraZeneca's PARP1 selective inhibitor was approved for clinical use in advanced malignant solid tumors
It is worth noting that this is a selective inhibitor of PARP1.
From CDE official website
PARP inhibitors have shown excellent clinical efficacy in homologous recombination-deficient cancer patients.
At the 2021AACR meeting, AstraZeneca disclosed the structure and early data of AZD5305 for the first time
In the preclinical toxicology model, AZD5305 showed superior properties to olaparib
In vitro, AZD5305 selectively inhibits the growth of DNA repair pathway-deficient cell lines, with IC50 in the single-digit nM range, while in other cells there is no or almost no growth inhibitory effect (IC50>10μM), which indicates that AZD5305 is clinically It has great potential for improved therapeutic index
From the AACR Annual Meeting
According to the Insight database, AZD5305 first started a phase 1 clinical PETRA study (NCT04644068) abroad in October 2020; and in China, this new drug was approved for clinical use for the first time today
From Insight Global New Drug Database (http://db.
Note: The original text has been deleted