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Microtubule inhibitor (specialist)

Eribulin

Brand names: Halaven

Eribulin is a synthetic halichondrin-derived microtubule inhibitor cytotoxic, used mainly in the treatment of locally advanced or metastatic breast cancer after prior chemotherapy.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It binds tubulin and inhibits microtubule growth without affecting shortening, sequestering tubulin into non-productive aggregates and arresting cells at the G2/M phase, triggering apoptosis.

Prescribing in practice

  • Myelosuppression, particularly neutropenia, is dose-limiting and can be severe; a full blood count must be checked before each dose and treatment delayed or reduced for cytopenias.
  • Prescribe and administer only under specialist oncology supervision as an intravenous infusion, with dose modification for hepatic and renal impairment.
  • It can cause peripheral neuropathy and QT-interval prolongation, so caution is needed with other QT-prolonging drugs and electrolyte disturbance.

Monitoring

Monitor full blood count before each cycle, alongside peripheral neuropathy, ECG/QT and electrolytes where indicated.

Counselling the patient

  • Report fever, sore throat or other signs of infection without delay, as your white cells may be low.
  • Tell your team about numbness, tingling or weakness in the hands or feet.
  • Effective contraception is required during and for a period after treatment.

Evidence & guidelines

The EMBRACE trial demonstrated an overall survival benefit for eribulin in heavily pre-treated metastatic breast cancer, and its use is informed by NICE technology appraisal guidance.

Reference: NICE TA423; NICE TA515; ESMO; SmPC; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.