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Active Pharma Ingredients / 29 Jul 2026

ANZURSTOBART

Generic Name: ANZURSTOBART

ABSTRACT -

Anzurstobart (formerly CC-95251 or BMS-986351) is an investigational monoclonal antibody directed against signal-regulatory protein alpha (SIRP-alpha) on macrophages and other myeloid cells. Blocking the SIRP-alpha-CD47 checkpoint is intended to remove a tumour-cell "do not eat me" signal and enhance macrophage-mediated phagocytosis, particularly when combined with tumour-opsonizing antibodies.

DOSAGE –

    • No approved standard dosage is established. Clinical studies have used intravenous, protocol-defined dose-escalation or expansion regimens, alone or with other anticancer medicines. Dose, infusion rate, premedication, and management of toxicity must follow the trial protocol.

SIDE EFFECTS –

  • Infusion-related fever, chills, flushing, or rash
  • Fatigue or weakness
  • Nausea or reduced appetite
  • Headache
  • Anaemia or other blood-count changes
  • Infection or immune-mediated inflammatory effects

ALLRGIC REACTIONS–

(These symptoms may indicate a serious allergic or infusion reaction and require medical attention.)

  • Hives or generalized rash
  • Swelling of the face, lips, tongue, or throat
  • Wheezing, breathing difficulty, or chest tightness
  • Severe infusion reaction or anaphylaxis

DRUG INTERACTIONS -

      • Formal interaction studies are limited
      • Other immune-active anticancer therapies may increase inflammatory toxicity
      • Myelosuppressive agents may increase blood-count abnormalities
      • Combination antibodies can change efficacy and toxicity; use protocol guidance

PRECAUTIONS –

  • Monitor during and after infusion for acute reactions
  • Check blood counts, infection signs, and organ function as specified
  • Screen for protocol-defined infection and immune-risk conditions
  • Use effective contraception and avoid breastfeeding as directed by the study

WARNINGS –

  • Clinical development status has changed over time and must be verified before use
  • Serious infusion, immune, infectious, or haematologic events are possible
  • Research-grade biosimilar products are not clinical medicines

 

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