ONCASPAR 3750IU - Pegaspargase by Servier

    ONCASPAR

    3750IU
    Oncology Medications

    ONCASPAR3750IU

    ONCASPAR (pegaspargase) 3750 IU is a PEGylated enzyme therapy used as part of multi-agent chemotherapy for the treatment of acute lymphoblastic leukemia (ALL) in both pediatric and adult patients.

    Generic Name:Pegaspargase
    Manufacturer:Servier

    Key Benefits

    • PEGylated formulation with extended half-life (5-7 days)
    • Less frequent dosing compared to native asparaginase
    • Reduced immunogenicity and fewer allergic reactions
    • Over 25 years of clinical experience in ALL treatment
    • Effective asparagine depletion for leukemia cell death
    • Suitable for patients hypersensitive to native asparaginase

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    How ONCASPAR Works

    1

    ONCASPAR (pegaspargase) works through a unique mechanism that exploits a metabolic vulnerability specific to acute lymphoblastic leukemia (ALL) cells:

    2

    **Asparagine Depletion Mechanism:** Asparagine is an amino acid essential for protein synthesis and cell survival. Normal healthy cells can produce their own asparagine using an enzyme called asparagine synthetase. However, ALL cancer cells have very low levels of this enzyme and cannot synthesize enough asparagine to survive—they must absorb it from the blood.

    3

    ONCASPAR is a modified form of the enzyme L-asparaginase. When injected, it circulates in the bloodstream and rapidly converts available asparagine into aspartic acid and ammonia. This depletes the asparagine supply in the blood, effectively starving ALL cells while normal cells continue to function using internally produced asparagine.

    4

    **PEGylation Technology:** The "PEG" in pegaspargase refers to polyethylene glycol chains attached to the enzyme. This PEGylation provides several advantages: • Extended half-life (5.5-7 days vs 1-2 days for native asparaginase) • Reduced immunogenicity and fewer allergic reactions • Less frequent dosing required (every 2-4 weeks vs multiple times weekly) • More consistent asparagine depletion over time

    5

    **Clinical Effect:** By maintaining asparagine depletion over extended periods, ONCASPAR prevents ALL cells from synthesizing proteins necessary for growth and division, leading to cell death (apoptosis). This mechanism synergizes with other chemotherapy agents in multi-agent treatment protocols.

    About ONCASPAR 3750IU

    ONCASPAR (pegaspargase) 3750 IU by Servier (formerly Baxalta/Shire) is a PEGylated form of the enzyme L-asparaginase that has been a cornerstone of acute lymphoblastic leukemia (ALL) treatment for over 25 years. This advanced formulation extends the half-life of native L-asparaginase through polyethylene glycol (PEG) modification, allowing for less frequent dosing while maintaining therapeutic efficacy. ONCASPAR works by depleting asparagine, an amino acid that leukemia cells cannot produce on their own. While normal cells can synthesize asparagine through asparagine synthetase, ALL cells lack this enzyme and depend entirely on external asparagine for survival. By eliminating circulating asparagine, ONCASPAR effectively starves leukemia cells while sparing normal tissues. As a licensed pharmaceutical supplier based in Turkey, Pharmacy Remedy provides authentic Servier ONCASPAR with complete cold chain handling, certificate of authenticity, and competitive wholesale pricing for hospitals, oncology/hematology clinics, and pharmaceutical distributors worldwide. ONCASPAR requires strict refrigerated storage at 2-8°C and must be handled by experienced healthcare professionals. Contact us via WhatsApp for current availability, bulk pricing, and international shipping options. ONCASPAR is FDA-approved as a component of multi-agent chemotherapy regimens for the treatment of: • First-line treatment of ALL in pediatric and adult patients • ALL patients who have developed hypersensitivity to native forms of L-asparaginase • Multi-agent chemotherapy protocols including induction, consolidation, and delayed intensification phases

    Common Uses

    • First-line acute lymphoblastic leukemia (ALL) treatment
    • Pediatric ALL multi-agent chemotherapy
    • Adult ALL combination treatment protocols
    • Patients with hypersensitivity to native L-asparaginase
    • ALL induction phase therapy
    • ALL consolidation phase treatment
    • ALL delayed intensification protocols

    Dosage Information

    ONCASPAR dosing should always be determined by a qualified hematologist/oncologist as part of a comprehensive ALL treatment protocol:

    Standard Dosing:

    • **Intramuscular (IM) or Intravenous (IV):** 2,500 IU/m² body surface area

    • **Frequency:** Every 14 days (as part of multi-agent chemotherapy)

    • **Maximum single dose:** Typically not to exceed manufacturer recommendations

    Administration Route:

    • **Intramuscular (IM):** Preferred route in many protocols; inject into large muscle mass

    • **Intravenous (IV):** Administer over 1-2 hours; do not give as bolus injection

    Treatment Phases:

    ONCASPAR is typically incorporated into various phases of ALL treatment:

    • **Induction Phase:** Initial intensive treatment to achieve remission

    • **Consolidation Phase:** Deepening remission after initial response

    • **Delayed Intensification:** Additional intensive therapy phase

    • **Maintenance:** Some protocols include during maintenance

    Important Considerations:

    • Premedication may be required to prevent infusion reactions

    • Monitor for signs of hypersensitivity during and after administration

    • Regular monitoring of pancreatic enzymes, coagulation, and liver function required

    • Dose modifications may be needed based on toxicity

    For Patients Previously Hypersensitive to E. coli Asparaginase:

    ONCASPAR may be used in patients who have had allergic reactions to native E. coli L-asparaginase, though careful monitoring is essential.

    *Note: One ONCASPAR vial contains 3,750 IU in 5 mL (750 IU/mL). Dosing is individualized based on body surface area.*

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

    Storage & Handling

    ONCASPAR requires strict cold chain storage to maintain stability and efficacy:

    Storage Temperature:

    • Store refrigerated at 2°C to 8°C (36°F to 46°F)

    • Do NOT freeze

    • Do NOT shake vigorously

    Protect from Light:

    • Keep in original carton until time of use

    • Protect from bright light

    Handling:

    • For single use only

    • Discard any unused portion

    • Do not use if solution is cloudy, discolored, or contains particles

    • Solution should be clear and colorless

    Reconstitution/Dilution:

    • Withdraw the calculated dose from the vial

    • For IV administration: Dilute in 100 mL of 0.9% Sodium Chloride or 5% Dextrose

    • Use diluted solution within 4 hours (room temperature) or 24 hours (refrigerated)

    Transportation:

    • Must maintain cold chain (2-8°C) during transport

    • Use validated cold chain packaging with temperature monitoring

    • Do not accept delivery if temperature excursion is suspected

    Shelf Life:

    • Check expiration date on packaging

    • Do not use beyond expiration date

    *Pharmacy Remedy ensures all ONCASPAR shipments maintain proper cold chain protocols with temperature monitoring and validated packaging for international delivery.*

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

    Frequently Asked Questions About ONCASPAR

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