Drug class
Anti-Androgen - Androgen Synthesis Inhibitors
Anti-Androgen - Androgen Synthesis Inhibitors is a therapeutic class of antineoplastic hormonal agents that suppress the body’s production of androgens rather than directly blocking the androgen receptor. Read more about Anti-Androgen - Androgen Synthesis Inhibitors
29 drugs in this class 26 manufacturers
Drugs in Anti-Androgen - Androgen Synthesis Inhibitors
ABIRATERONE ACETATE
ABIRATERONE ACETATE
ABIRATERONE ACETATE
ABIRATERONE ACETATE
ABIRTEGA (abiraterone acetate)
ABIRATERONE ACETATE
ABIRATERONE ACETATE
ABIRATERONE ACETATE
Anti-Androgen - Androgen Synthesis Inhibitors is a therapeutic class of antineoplastic hormonal agents that suppress the body’s production of androgens rather than directly blocking the androgen receptor.
These medications, exemplified by abiraterone acetate, work primarily by selectively inhibiting the cytochrome P450 17A1 (CYP17) enzyme complex, thereby halting steroid biosignaling in the testes, adrenal glands, and tumor tissue itself.
By depleting serum and intratumoral levels of testosterone and dihydrotestosterone, this class is primarily utilized in the management of advanced prostate cancer, particularly metastatic castration-resistant and castration-sensitive prostate cancer.
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connectrx.com
Anti-Androgen - Androgen Synthesis Inhibitors is a therapeutic class of antineoplastic hormonal agents that suppress the body’s production of androgens rather than directly blocking the androgen receptor These medications, exemplified by abiraterone acetate, work primarily by selectively inhibiting the cytochrome P450 17A1 (CYP17) enzyme complex, thereby halting steroid biosignaling in the testes, adrenal glands, and tumor tissue itself
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mdpi.com
Anti-Androgen - Androgen Synthesis Inhibitors is a therapeutic class of antineoplastic hormonal agents that suppress the body’s production of androgens rather than directly blocking the androgen receptor By depleting serum and intratumoral levels of testosterone and dihydrotestosterone, this class is primarily utilized in the management of advanced prostate cancer, particularly metastatic castration-resistant and castration-sensitive prostate cancer
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nih.gov
These medications, exemplified by abiraterone acetate, work primarily by selectively inhibiting the cytochrome P450 17A1 (CYP17) enzyme complex, thereby halting steroid biosignaling in the testes, adrenal glands, and tumor tissue itself By depleting serum and intratumoral levels of testosterone and dihydrotestosterone, this class is primarily utilized in the management of advanced prostate cancer, particularly metastatic castration-resistant and castration-sensitive prostate cancer
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oaepublish.com
These medications, exemplified by abiraterone acetate, work primarily by selectively inhibiting the cytochrome P450 17A1 (CYP17) enzyme complex, thereby halting steroid biosignaling in the testes, adrenal glands, and tumor tissue itself By depleting serum and intratumoral levels of testosterone and dihydrotestosterone, this class is primarily utilized in the management of advanced prostate cancer, particularly metastatic castration-resistant and castration-sensitive prostate cancer
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