RLAY stock soars on positive interim efficacy data from the early-stage study of its doublet therapy, RLY-2608 in combination with Faslodex, for treating MBC.

The FDA’s clearance could double Kisqali’s breast cancer market. Elsewhere, Novo is exploring new ways to deliver genetic ...

Pfizer’s atirmociclib, a CDK4 inhibitor, is undergoing phase III development to treat HR+/HER2- MBC. Novartis’ Kisqali, a ...

The FDA approved ribociclib (Kisqali) for adjuvant treatment of high-risk ... Patients with advanced or metastatic breast cancer had a recommended oral dose of 600 mg tablets that were received once ...

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Track all markets on TradingView Specifically, financial services firm Needham initiated coverage on SMCI with a Buy rating and $600 price target, calling it the "coolest kid in AI town." ...

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The US FDA has approved Kisqali (ribociclib) for treating early-stage breast cancer in combination with hormone therapy. It targets high-risk HR-positive, HER2-negative stage II and III patients ...

Wall Street’s staged a comeback Wednesday as a boost from the technology sector offset investor disappointment at the early morning inflation report, which crushed hopes the Federal Reserve ...

Findings from the NATALEE trial show that the combination of Kisqali and an aromatase inhibitor resulted in disease-free benefits in a breast cancer subset. For patients with hormone receptor ...

Kisqali has been FDA-approved with an aromatase inhibitor as postsurgical treatment for some with early breast cancer at a high risk of recurrence. The Food and Drug Administration (FDA) has approved ...