eribulin (Halaven)

Other Medications · Approved since 2010

US Off-label EU EMA Approved ES Funded by SNS off-label in CRC IV 2 Clinical Trials
Microtubules tubulin

Description

Eribulin is a synthetic analog of halichondrin B, classified as a microtubule dynamics inhibitor chemotherapy agent. It is primarily FDA-approved for metastatic breast cancer and liposarcoma, but has been explored in colorectal cancer through clinical trials. In CRC, eribulin is typically considered for patients with advanced disease who have progressed on standard therapies, particularly in the context of HER2-positive tumors or as part of combination regimens.

Mechanism of Action

Eribulin works by binding to the plus ends of microtubules and inhibiting microtubule polymerization without affecting depolymerization, leading to irreversible mitotic blockade. This unique mechanism differs from other microtubule-targeting agents, as it sequesters tubulin into nonproductive aggregates and triggers apoptosis through prolonged mitotic arrest.

Molecular Targets

Side Effects

Neutropenia Peripheral neuropathy Fatigue Alopecia Nausea Constipation Anorexia Muscle weakness Pyrexia

Not all side effects are listed. Side effects vary by individual. Always consult your oncologist.

Clinical Trials

NCT05824975 Phase 1
Recruiting
A Study to Evaluate the Safety and Therapeutic Activity of GI-102 As a Single Agent and in Combination with Conventional Anti-cancer Drugs, Pembrolizumab or Trastuzumab Deruxtecan(T-DXd) in Patients with Advanced Solid Tumors (KEYNOTE-G08)
United States, South Korea
NCT06328738 Phase 1
Active, not recruiting
ELVN-002 With Trastuzumab +/- Chemotherapy in HER2+ Solid Tumors, Colorectal and Breast Cancer
United States, Belgium, France, Italy, Netherlands, South Korea, Spain