Overview
Ixabepilone is an epothilone B analog developed by Bristol-Myers Squibb as a cancer drug. It was FDA approved on October 16, 2007, for the treatment of unresponsive aggressive metastatic or locally advanced breast cancer. Ixabepilone is administered through injection, and will be marketed under the trade name Ixempra. Ixabepilone is a semisynthetic analogue of epothilone B. It has a lactone–lactam modification that minimizes susceptibility to esterase degradation.
Indication
用于在其他化学治疗均失效后作为治疗晚期乳腺癌的药物。
Associated Conditions
- Locally Advanced Breast Cancer (LABC)
- Metastatic Breast Cancer
Clinical Trials
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Title | Posted | Study ID | Phase | Status | Sponsor |
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2008/11/14 | Phase 2 | Terminated | Hellenic Cooperative Oncology Group | ||
2008/11/13 | Phase 3 | Completed | |||
2008/11/05 | Phase 3 | Completed | |||
2008/10/03 | Phase 1 | Terminated | |||
2008/09/12 | Phase 2 | Completed | |||
2008/08/27 | Phase 2 | Completed | |||
2008/07/17 | Phase 1 | Completed | Medstar Health Research Institute | ||
2008/05/06 | Phase 2 | Terminated | |||
2008/03/18 | Phase 1 | Completed | |||
2008/03/12 | Phase 2 | Completed | R-Pharm |
FDA Drug Approvals
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No FDA approvals found for this drug. |
EMA Drug Approvals
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HSA Drug Approvals
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NMPA Drug Approvals
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PPB Drug Approvals
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TGA Drug Approvals
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