About Eribulin Mesylate (Available For Selected Markets) API
Therapeutic Category Oncology

CAS Number
441045-17-6
API Technology
Synthetic
Dose Form
Injectable
Dr Reddy's Development Status
Available
Available Regulatory Filing
USDMF, EUDMF, Canada DMF
Mechanism of Action
Eribulin inhibits the growth phase of microtubules without affecting the shortening phase and sequesters tubulin into nonproductive aggregates. Eribulin exerts its effects via a tubulin-based antimitotic mechanism leading to G 2/M cell-cycle block, disruption of mitotic spindles, and, ultimately, apoptotic cell death after prolonged mitotic blockage.
In addition, eribulin treatment of human breast cancer cells caused changes in morphology and gene expression as well as decreased migration and invasiveness in vitro. In mouse xenograft models of human breast cancer, eribulin treatment was associated with increased vascular perfusion and permeability in the tumor cores, resulting in reduced tumor hypoxia, and changes in the expression of genes in tumor specimens associated with a change in phenotype.
Indication
HALAVEN is a microtubule inhibitor indicated for the treatment of patients with:
- Metastatic breast cancer who have previously received at least two chemotherapeutic regimens for the treatment of metastatic disease. Prior therapy should have included an anthracycline and a taxane in either the adjuvant or metastatic setting.
- Unresectable or metastatic liposarcoma who have received a prior anthracycline-containing regimen.
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FAQs
Precautions with history of liver, kidney, heart problems, any allergy, who are taking other medications, during pregnancy and breastfeeding.
Eribulin injection is used to treat metastatic (cancer that has already spread to other parts of the body) breast cancer
Eribulin belongs to class-III of BCS classification.
Eribulin API have DMFs available for USDMF, Europe and Canada.
Eribulin should be stored at -65 ± 10 ºC temperature.
The available dosage form for Eribulin is 1 mg/2mL (0.5MG/ML).