BLINCYTO 35mcg - Blinatumomab by Amgen

    BLINCYTO

    35mcg
    Oncology Medications

    BLINCYTO35mcg

    BLINCYTO (Blinatumomab) 35mcg is a first-in-class BiTE® antibody by Amgen for B-cell precursor acute lymphoblastic leukemia (ALL).

    Generic Name:Blinatumomab
    Manufacturer:Amgen

    Key Benefits

    • First-in-class BiTE® antibody — revolutionary mechanism of action
    • Significantly improved OS vs chemotherapy (TOWER trial: 7.7 vs 4.0 months)
    • High MRD response rate (78% in BLAST trial)
    • Practice-changing E1910 results in frontline ALL
    • Off-the-shelf availability (no manufacturing delay like CAR-T)
    • Active at picomolar concentrations

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    How BLINCYTO Works

    1

    Blinatumomab is a BiTE® (bispecific T-cell engager) antibody construct consisting of two single-chain variable fragments (scFv) connected by a short linker peptide. One scFv binds to CD19 on B-cell leukemia cells, while the other binds to CD3 on T-cells.

    2

    By simultaneously binding both targets, blinatumomab creates a direct immunological synapse between the patient's T-cells and the cancer cells. This activates endogenous T-cell cytotoxicity, leading to lysis of CD19-positive leukemic blasts through perforin/granzyme-mediated killing.

    3

    This mechanism is unique because it bypasses MHC-restricted antigen presentation, enabling potent anti-leukemic activity at picomolar concentrations. The small size of the BiTE construct (~55 kDa) also allows it to bridge cells more efficiently than conventional antibodies.

    About BLINCYTO 35mcg

    BLINCYTO (blinatumomab) 35mcg powder for solution for infusion by Amgen is the world's first bispecific T-cell engager (BiTE®) antibody approved for clinical use. It represents a revolutionary approach to immunotherapy by redirecting the patient's own T-cells to recognize and destroy CD19-positive leukemic cells. Blincyto is approved for relapsed or refractory B-cell precursor ALL in adults and children, and for ALL in first or second complete remission with minimal residual disease (MRD) ≥0.1%. The landmark TOWER trial demonstrated significant overall survival benefit, and the E1910/ECOG trial established Blincyto as part of frontline ALL treatment. As a licensed pharmaceutical supplier based in Turkey, we provide authentic Amgen BLINCYTO with validated cold chain shipping (2-8°C), certificate of authenticity, and competitive wholesale pricing for hospitals and hematology centers worldwide.

    Common Uses

    • Relapsed or refractory Ph- B-cell precursor ALL (adults and children)
    • Ph- B-cell precursor ALL in CR1/CR2 with MRD ≥0.1%
    • Frontline ALL consolidation (per E1910 data)

    Dosage Information

    BLINCYTO dosing varies by indication:

    Relapsed/Refractory ALL (Adults ≥45kg):

  1. Cycle 1: 9 mcg/day (Days 1-7), then 28 mcg/day (Days 8-28)
  2. Cycle 2+: 28 mcg/day (Days 1-28)
  3. 14-day treatment-free interval between cycles
  4. MRD-Positive ALL:

  5. 28 mcg/day (Days 1-28) for all cycles
  6. Up to 4 cycles of treatment
  7. Administered as continuous intravenous infusion over 24 hours using an infusion pump. Each vial contains 35 mcg blinatumomab.

    Always consult with a qualified healthcare professional for proper dosing. This information is for reference only.

    Storage & Handling

    Store at 2-8°C (36-46°F). Do not freeze. Protect from light. Store in original packaging. After reconstitution: stable up to 96 hours at 2-8°C or 48 hours at room temperature (≤27°C). Validated cold chain required for shipping.

    We ensure proper cold chain handling during shipping to maintain product integrity.

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