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Active Pharma Ingredients / 22 Sep 2026

CEVOSTAMAB

Generic Name: CEVOSTAMAB

ABSTRACT -

Cevostamab (BFCR4350A) is an investigational bispecific antibody targeting FcRH5 (Fc receptor homologue 5, a B-lineage antigen) on myeloma cells and CD3 on T cells, developed by Genentech/Roche for relapsed/refractory multiple myeloma. It redirects cytotoxic T lymphocytes to lyse FcRH5-expressing myeloma cells. Phase I data (CEVOSTAMAB study) demonstrated anti-myeloma activity and is being further evaluated in Phase I/II trials.

DOSAGE -

Intravenous infusion; step-up dosing schedule (e.g., 0.3 mg → 1 mg → 3.6 mg → target dose) to mitigate cytokine release syndrome; Q3W or Q2W maintenance dosing per protocol.

SIDE EEFECTS -

  • Cytokine release syndrome (CRS)
  • Fatigue
  • Fever
  • Cytopenias
  • Infections

ALLERGIC REACTIONS -

These symptoms may indicate an allergic reaction and require immediate medical attention.

  • Infusion hypersensitivity
  • Anaphylaxis
  • Urticaria
  • Angioedema

DRUG INTERACTIONS-

  • Corticosteroids used for CRS — may reduce T-cell activity
  • Avoid live vaccines during treatment
  • Additive myelosuppression with other myeloma therapies

PREAUTONS–

  • Administer in hospital setting with CRS monitoring for all step-up doses
  • ICANS (neurotoxicity) monitoring required
  • Thromboprophylaxis per myeloma management guidelines
  • Effective contraception required

WARNINGS –

  • Severe CRS including Grade ≥3 reported — tocilizumab and corticosteroids must be available
  • Tumour lysis syndrome risk in high disease burden patients
  • Embryo-foetal toxicity — avoid in pregnancy

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