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Ipilimumab Injection
Ipilimumab was approved by the U.S. Food and Drug Administration (FDA) in March 2011, to treat people with late-stage melanoma that has spread or cannot be removed by surgery.

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ipilimumab injection, for intravenous use

  • API: ipilimumab
  • Trade Name: On Request
  • Packaging: injection, for intravenous use
  • Strength: Injection: 50 mg/10 mL (5 mg/mL) and 200 mg/40 mL (5 mg/mL) in a single-use vial.
  • Indications:


Ipilimumab is a human cytotoxic T-lymphocyte antigen 4 (CTLA-4)-blocking antibody indicated for:

  •  Treatment of unresectable or metastatic melanoma in adults and pediatric patients (12 years and older).
  • Adjuvant treatment of patients with cutaneous melanoma with pathologic involvement of regional lymph nodes of more than 1 mm who have undergone complete resection, including total lymphadenectomy.
  • Treatment of patients with intermediate or poor risk, previously untreated advanced renal cell carcinoma, in combination with nivolumab.

Note: (see Drugs@FDA for complete indication)


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