Ribociclib

Generic Name
Ribociclib
Brand Names
Kisqali 200 Mg Daily Dose Carton, Kisqali Femara Co-pack, Kisqali
Drug Type
Small Molecule
Chemical Formula
C23H30N8O
CAS Number
1211441-98-3
Unique Ingredient Identifier
TK8ERE8P56
Background

Ribociclib is a selective cyclin-dependent kinase inhibitor, a class of drugs that help slow the progression of cancer by inhibiting two proteins called cyclin-dependent kinase 4 and 6 (CDK4/6). These proteins, when over-activated, can enable cancer cells to grow and divide too quickly. Targeting CDK4/6 with enhanced precision may play a role in ensuring tha...

Indication

用于联合芳香酶抑制剂或氟维司群治疗激素受体(HR)阳性、人表皮生长因子受体2(HER2)阴性的晚期或转移性乳腺癌成人患者。

Associated Conditions
Advanced Breast Cancer, Metastatic Breast Cancer
Associated Therapies
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finance.yahoo.com
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EC Approves NVS' Kisqali for a Broad Population in Early Breast Cancer

The EC approved Novartis' Kisqali for HR+/HER2- early breast cancer, reducing recurrence risk by 25.1%.

EC approves Novartis' Kisqali for HR+/HER2– early breast cancer

Novartis receives EC approval for Kisqali (ribociclib) to treat early breast cancer at high risk of recurrence. Kisqali, a CDK inhibitor, is now approved in combination with an aromatase inhibitor for HR+/HER2- EBC patients. The approval is based on the Phase 3 NATALEE trial, showing a 25.1% reduction in disease recurrence risk with Kisqali plus endocrine therapy compared to endocrine therapy alone.
novartis.com
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Novartis Kisqali® receives European Commission approval in a broad population of patients

EC approves Kisqali® (ribociclib) plus AI for HR+/HER2- early breast cancer, based on Phase III NATALEE trial showing 25.1% reduction in recurrence risk. Approval extends eligibility to more patients, addressing high risk of recurrence despite endocrine therapy.

EC approves Novartis' Kisqali to treat early breast cancer

The European Commission approved Novartis' Kisqali, in combination with an aromatase inhibitor, for the adjuvant treatment of high-risk, hormone receptor-positive, HER2-negative breast cancer. This decision is based on the Phase III NATALEE trial results, showing a 25.1% decrease in disease recurrence risk. The approval follows the US FDA's recent approval for the same indication.
pmlive.com
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Novartis' Kisqali granted EC approval to treat early breast cancer patients

Novartis’ Kisqali approved by EC to reduce early breast cancer recurrence risk in HR-positive, HER2-negative patients, based on NATALEE trial results showing 25.1% reduction in recurrence risk with Kisqali plus endocrine therapy.
globenewswire.com
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Novartis Kisqali® receives European Commission approval

EC approves Kisqali (ribociclib) plus AI for HR+/HER2- EBC at high risk of recurrence, based on NATALEE trial results showing 25.1% reduction in disease recurrence risk with Kisqali plus ET vs. ET alone, consistent across subgroups.

European Commission gives nod to Novartis' novel therapy to treat breast cancer

Novartis announces EC approval of Kisqali for early breast cancer, based on NATALEE trial results showing 25.1% reduction in recurrence risk. The approval addresses a key unmet need for patients at high risk of cancer return.
marketscreener.com
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Novartis highlights new 96-week results from Phase III Scemblix ASC4FIRST trial at ASH

Novartis to present over 65 abstracts at ASH and SABCS, highlighting commitment to cancer and blood disorder treatments, with an art exhibit at SABCS featuring personal breast cancer stories.
pharmabiz.com
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Novartis highlights new 96-week results from phase III Scemblix ASC4FIRST trial at ASH

Novartis presents over 65 abstracts at ASH and SABCS, highlighting new data on Scemblix, Kisqali, and other treatments, emphasizing commitment to cancer and blood disorder patients. The company also showcases personal breast cancer stories at SABCS, aiming to uplift and unite the community.
biospace.com
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Novartis highlights new 96-week results from Phase III Scemblix® ASC4FIRST trial at ASH

Novartis to present over 65 abstracts at ASH and SABCS, including 96-week Scemblix results and Kisqali 4-year analysis. Data highlights commitment to cancer and blood disorder treatments.
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