Yervoi 50mg, Ipilimumab Injection, AntiCancer Drugs, Immunotherapy, Online Pharmacy
AntiCancer Drugs Liver Cancer Head/Neck Cancer Kidney Cancer Skin Cancer Lung Cancer

Yervoi 50mg, Solution for Injection - 10ml

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Drug Type Original
Active Ingredient IPILIMUMAB
Strength 50MG
Manufacturer BRISTOL MYERS SQUIBB
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Product Description

Yervoi 50mg, Solution for Injection contains Ipilimumab, a fully human monoclonal antibody targeting cytotoxic T-lymphocyte antigen-4 (CTLA-4). As a checkpoint inhibitor, it enhances antitumor immunity by sustaining T-cell activation and proliferation. Ipilimumab is a critical component of combination immunotherapy regimens, particularly with Nivolumab, for various malignancies. It is widely used in both metastatic and adjuvant settings across melanoma, renal cell carcinoma, colorectal cancer, NSCLC, and other cancer types.

Indications & Uses

  • AntiCancer Drugs > Skin Cancer (Melanoma)
    Indicated for unresectable or metastatic melanoma, as well as adjuvant treatment in high-risk resected cases. By blocking CTLA-4, Ipilimumab promotes sustained T-cell mediated destruction of melanoma cells.

  • Lung Cancer (NSCLC, Mesothelioma)
    Used in combination with Nivolumab and platinum-doublet chemotherapy for first-line treatment of metastatic NSCLC and malignant pleural mesothelioma, improving progression-free survival and durable response rates.

  • Head and Neck Squamous Cell Carcinoma (HNSCC), Esophageal Cancer
    Ipilimumab plus Nivolumab offers a checkpoint blockade regimen in PD-L1 positive or recurrent/metastatic HNSCC and advanced esophageal squamous cell carcinoma, especially after prior therapy.

  • Liver Cancer (Hepatocellular Carcinoma)
    Used post-sorafenib in patients with advanced HCC. The combination with Nivolumab restores antitumor immunity by targeting multiple immune checkpoints.

  • Kidney Cancer (Renal Cell Carcinoma)
    Indicated as first-line therapy in combination with Nivolumab for advanced RCC. Enhances tumor rejection in intermediate- and poor-risk patients.

  • Colorectal Cancer (MSI-H/dMMR)
    Approved for metastatic microsatellite instability-high or mismatch repair-deficient colorectal cancer, offering durable disease control after chemotherapy failure.

  • Others (Pediatric Melanoma and mCRC, Off-label Solid Tumors)
    Used in adolescents ≥12 years with advanced melanoma or mCRC. Emerging studies support use in refractory or biomarker-positive malignancies.

Benefits & Effectiveness

  • Blocks the inhibitory receptor CTLA-4 on activated T cells, allowing prolonged T-cell proliferation and enhanced tumor cell lysis
  • Modulates host immune response rather than directly targeting tumor cells
  • Synergizes with PD-1 inhibitors like Nivolumab for broader immune activation across tumor microenvironments
  • Contributes to long-term remission in a subset of patients

Directions for Use

  • Melanoma: Monotherapy: 3 mg/kg IV every 3 weeks × 4 doses. Combo: 3 mg/kg IV q3w × 4 doses with Nivolumab (or until toxicity). Adjuvant: 10 mg/kg IV q3w × 4 doses, then q12w up to 3 years.

  • Renal Cell Carcinoma: 1 mg/kg IV q3w × 4 doses with Nivolumab 3 mg/kg.

  • Colorectal Cancer (MSI-H/dMMR): 1 mg/kg IV q3w × 4 doses + Nivolumab.

  • Hepatocellular Carcinoma: 3 mg/kg IV q3w × 4 doses + Nivolumab 1 mg/kg.

  • NSCLC: 1 mg/kg IV q6w with Nivolumab 360 mg q3w + 2 cycles of chemotherapy.

  • Malignant Pleural Mesothelioma: 1 mg/kg IV q6w + Nivolumab 360 mg q3w.

  • Esophageal SCC: 1 mg/kg IV q6w + Nivolumab q2w or q3w.

  • Pediatric (≥12 yrs): Melanoma: 3 mg/kg IV q3w × 4 doses (mono or with Nivolumab 1 mg/kg). mCRC: 1 mg/kg IV q3w × 4 doses + Nivolumab 3 mg/kg.

    All infusions should be administered over 30 minutes. Therapy may continue with Nivolumab monotherapy after the Ipilimumab phase. Confirm PD-L1, MSI, or BRAF status as per indication-specific requirements.

Storage

  • Store in a refrigerator at 2°C to 8°C.
  • Do not freeze.
  • Protect from light.
  • Once opened, use immediately and discard any unused portion.

Possible Side Effects

  • Common immune-related: colitis, dermatitis, hepatitis, endocrinopathies (hypothyroidism, adrenal insufficiency) – early detection is essential; corticosteroids may be required
  • Other: fatigue, rash, diarrhea, infusion reactions
  • Monitoring: liver enzymes, thyroid function, and renal panels should be assessed routinely

FAQs

It is used to treat melanoma, NSCLC, RCC, colorectal cancer, HCC, and other cancers, either as monotherapy or in combination with nivolumab.
It is given as an intravenous infusion, typically every 3 or 6 weeks depending on the cancer type and treatment protocol.
It is approved for use in pediatric patients ≥12 years for melanoma and certain colorectal cancers.
Yes, depending on the indication. Testing for PD-L1, MSI status, or BRAF mutations may be necessary to guide eligibility and response prediction.
Yes, especially in adjuvant melanoma and other tumors where maintenance with nivolumab continues up to 2–3 years based on tolerability and benefit.

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