Ibrance vs Kisqali
Side-by-side comparison of Ibrance and Kisqali — mechanism, indications, safety, trials, sponsor, and pricing.
At a glance
| Ibrance | Kisqali |
| Generic name | Palbociclib | ribociclib |
| Sponsor | Pfizer | Novartis |
| Drug class | CDK4/6 inhibitor | CDK4/6 inhibitor; aromatase inhibitor |
| Molecular target | Cyclin-dependent kinases 4 and 6 (CDK4/6) | Cyclin-dependent kinase (CDK) 4 and 6; aromatase enzyme |
| Modality | Small molecule | — |
| Phase | FDA-approved | FDA-approved |
| Therapeutic area | Oncology | Oncology |
| First approval | 2015 | 2017 |
Mechanism of action
| Ibrance | Palbociclib inhibits CDK4/6 to block G1/S cell cycle progression in ER-positive breast cancer. |
| Kisqali | Ribociclib inhibits CDK4/6 kinases to arrest G1 cell cycle phase; letrozole inhibits aromatase to reduce estrogen biosynthesis. |
Approved indications
Ibrance
- Hormone receptor positive malignant neoplasm of breast
- Human epidermal growth factor 2 negative carcinoma of breast
Kisqali
- Hormone receptor positive malignant neoplasm of breast
Common side effects
Ibrance
- Neutrophil count decreased
- Fatigue
- Diarrhea
- Platelet count decreased
- Nausea
- Neutropenia
- Headache
- Aspartate aminotransferase increased
Kisqali
- Neutropenia
- Nausea
- Fatigue
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Leukopenia
- Arthralgia
- Headache
Further reading