News about "Trodelvy"

US FDA Approves KEYTRUDA and KEYTRUDA QLEX, Each with Trodelvy

US FDA Approves KEYTRUDA and KEYTRUDA QLEX, Each with Trodelvy

The US Food and Drug Administration (FDA) has approved KEYTRUDA and KEYTRUDA QLEX in combination with Trodelvy as first-line treatment for adults with PD-L1-positive (CPS ≥10) advanced Triple-Negative Breast Cancer (TNBC).

Trodelvy | 26/06/2026 | By News Bureau 177

US FDA Approves KEYTRUDA and KEYTRUDA QLEX, Each with Trodelvy

US FDA Approves KEYTRUDA and KEYTRUDA QLEX, Each with Trodelvy

The US Food and Drug Administration (FDA) has approved KEYTRUDA and KEYTRUDA QLEX in combination with Trodelvy as first-line treatment for adults with PD-L1-positive (CPS ≥10) advanced Triple-Negative Breast Cancer (TNBC).

Trodelvy | 26/06/2026 | By News Bureau 177

European Commission Approves Gilead's Trodelvy as First-Line Treatment for Metastatic Triple-Negative Breast Cancer

European Commission Approves Gilead's Trodelvy as First-Line Treatment for Metastatic Triple-Negative Breast Cancer

The European Commission has approved Trodelvy for first-line treatment of unresectable or metastatic triple-negative breast cancer, offering a new therapeutic option for patients with one of the most aggressive forms of breast cancer.

Trodelvy | 25/06/2026 | By News Bureau

Gilead Sciences and Kite Pharma to Highlight Oncology Progress at ASCO and EHA 2026 with ADC and Cell Therapy Data

Gilead Sciences and Kite Pharma to Highlight Oncology Progress at ASCO and EHA 2026 with ADC and Cell Therapy Data

Gilead Sciences and Kite Pharma to present new ASCO and EHA 2026 data highlighting progress in Antibody Drug Conjugates (ADCs) and CAR T-cell therapies, including updates on Trodelvy and anito-cel for difficult-to-treat cancers.

Trodelvy | 22/05/2026 | By News Bureau 511


 

 

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