Few medications have redefined hormonal therapy as decisively as anastrozole did following its release in 1995. Developed by Zeneca, it functioned by selectively inhibiting aromatase, thereby reducing estrogen levels systemically. Its precision and lack of estrogenic side activity distinguished it from drugs like tamoxifen. Widespread adoption followed the results of the ATAC trial, one of the most comprehensive head-to-head studies in hormonal oncology, which confirmed its superiority in relapse prevention.
Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.
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Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.
Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.
Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.