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Peg L Asparaginase Injection (L-ASPARA)

Peg L Asparaginase Injection (L-ASPARA)
Peg L Asparaginase Injection (L-ASPARA)

Peg L Asparaginase Injection (L-ASPARA) Specification

  • Storage Instructions
  • Store at 2C to 8C, protect from light, do not freeze
  • Accuracy
  • Pharmaceutical grade
  • Instruments Type
  • Injection
  • Features
  • PEGylated enzyme for increased half-life; Ready to use
  • Frequency
  • As per physician prescription and treatment protocol
  • Shelf Life
  • 24 months from date of manufacture
  • Function
  • Depletes L-asparagine to inhibit leukemia cell growth
  • Usage Type
  • Clinical and hospital use
  • Equipment Type
  • Pharmaceutical Injection
  • Material
  • Sterile solution
  • Condition
  • New
  • Technology
  • Recombinant DNA technology
  • Portable
  • Yes
  • Wall Mounted
  • No
  • Operating Type
  • Parenteral (Intravenous/Intramuscular)
  • Use
  • Treatment of Acute Lymphoblastic Leukemia (ALL)
  • Color
  • Colorless to pale yellow solution
  • Brand Name
  • L-ASPARA
  • Administration Route
  • Intravenous or Intramuscular injection
  • Prescription Required
  • Yes
  • Dosage Form
  • Injection
  • Composition
  • PEGylated L-Asparaginase
  • Indication
  • Acute Lymphoblastic Leukemia (ALL), Lymphoblastic Lymphoma
  • Type of Packaging
  • Glass Vial
  • Export Market
  • Global
  • CTD/Non-CTD
  • CTD Complaints
  • Strength
  • 3750 IU
  • Packing Type
  • Single-use Vial (5 ml)
  • MSDS Available
  • Yes
  • Formulation
  • Lyophilized powder reconstituted for solution for injection
  • Drug Content
  • Peg L Asparaginase 3750 IU/5ml
 

Peg L Asparaginase Injection (L-ASPARA) Trade Information

  • Minimum Order Quantity
  • 100 Packs
  • FOB Port
  • AHMEDABAD
  • Payment Terms
  • Paypal, Cash Advance (CA), Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • Delivery Time
  • 3 Days
  • Sample Policy
  • Sample costs shipping and taxes has to be paid by the buyer
  • Packaging Details
  • Box
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
 

About Peg L Asparaginase Injection (L-ASPARA)

Peg L-Asparaginase Injection (L-ASPARA) is an enzyme-based medication used primarily in the treatment of acute lymphoblastic leukemia (ALL), a type of cancer that affects the blood and bone marrow. It is a pegylated form of asparaginase, which means it has been chemically modified with polyethylene glycol (PEG) to extend its half-life in the body, allowing for less frequent administration compared to non-pegylated asparaginase.

How it works:

  • Asparaginase works by breaking down asparagine, an amino acid that is essential for the growth and survival of leukemia cells. Many cancerous cells, especially those in leukemia, depend on asparagine for their growth.
  • By depleting asparagine, Peg L-Asparaginase disrupts the cancer cells' ability to proliferate, effectively killing or preventing the growth of these abnormal cells.

Common uses:

  • Acute lymphoblastic leukemia (ALL): It is often used as part of a chemotherapy regimen for treating ALL in both children and adults.
  • It may also be used in combination with other chemotherapy agents to treat various types of leukemia or lymphomas.

Dosage and administration:

  • Peg L-Asparaginase is typically administered through an intravenous (IV) injection or, in some cases, as an intramuscular (IM) injection.
  • The dose and frequency depend on the specific treatment protocol and the patient's condition. Typically, it is given once every 1421 days as part of a multi-drug chemotherapy regimen.
  • Infusion rates and procedures will be carefully managed by healthcare professionals, often in a hospital or specialized setting.

Possible side effects:

  • Allergic reactions: Some patients may develop allergic reactions, ranging from mild symptoms (rash, fever) to severe reactions (anaphylaxis). Pre-medications like antihistamines or steroids may be given to reduce these risks.
  • Liver function abnormalities: Asparaginase can affect liver enzymes, so liver function will be closely monitored during treatment.
  • Pancreatitis: Inflammation of the pancreas can occur and requires careful monitoring.
  • Blood clotting issues: Since asparaginase can affect clotting factors, blood clotting issues or bleeding may arise.
  • Other side effects: Nausea, vomiting, fatigue, and changes in blood sugar levels may also occur.

Important considerations:

  • Pre-treatment testing: Before starting Peg L-Asparaginase, liver function tests and allergy assessments are typically conducted.
  • Hydration and monitoring: Close monitoring of kidney and liver function is necessary, as well as observation for allergic reactions.
  • Pregnancy and breastfeeding: This medication is generally not recommended during pregnancy or breastfeeding unless absolutely necessary, as it can harm a developing fetus or infant.

Monitoring and follow-up:

  • Regular blood tests (including liver and kidney function tests, blood counts) are necessary to ensure safe use.
  • Treatment regimens are typically individualized, so close communication with the healthcare team is vital throughout therapy.


Advanced Therapy for Leukemia

L-ASPARA leverages recombinant DNA technology and PEGylation to deliver a potent and prolonged treatment for patients with Acute Lymphoblastic Leukemia (ALL) and Lymphoblastic Lymphoma. Its increased half-life ensures sustained therapeutic efficacy, minimizing the frequency of dosing and maximizing patient comfort during treatment.


Strict Quality and Safety Standards

Manufactured in compliance with pharmaceutical-grade specifications and CTD requirements, L-ASPARA is supplied as a sterile, lyophilized powder in glass vials. The product features detailed storage instructions and a comprehensive MSDS, ensuring safety, efficacy, and consistency for clinical and hospital use worldwide.

FAQ's of Peg L Asparaginase Injection (L-ASPARA):


Q: How is L-ASPARA (Peg L Asparaginase Injection) administered to patients?

A: L-ASPARA can be administered either intravenously or intramuscularly by healthcare professionals. The lyophilized powder is first reconstituted with the appropriate solvent as instructed before injection.

Q: What is the main benefit of using PEGylated L-Asparaginase in leukemia treatment?

A: The PEGylation process increases the enzyme's half-life in the body, providing prolonged therapeutic activity and reducing the frequency of dosing, which improves patient adherence and outcomes.

Q: When should L-ASPARA therapy be initiated for patients diagnosed with ALL or Lymphoblastic Lymphoma?

A: L-ASPARA should be initiated upon prescription by a qualified physician, following an established treatment protocol for Acute Lymphoblastic Leukemia (ALL) or Lymphoblastic Lymphoma.

Q: Where should L-ASPARA be stored prior to use?

A: The product must be stored between 2C and 8C, protected from light, and must not be frozen to maintain its stability and efficacy.

Q: What is the process for preparing L-ASPARA Injection for administration?

A: L-ASPARA comes as a lyophilized powder in a glass vial. Before administration, it must be reconstituted with the recommended solvent to prepare a sterile, ready-to-use solution.

Q: Who can receive L-ASPARA treatment and is a prescription required?

A: L-ASPARA is indicated for patients with Acute Lymphoblastic Leukemia (ALL) or Lymphoblastic Lymphoma and should only be used under prescription and medical supervision in clinical settings.

Q: What is the shelf life and storage instruction for L-ASPARA?

A: L-ASPARA has a shelf life of 24 months from the date of manufacture. To preserve its potency, it should be kept refrigerated (2C to 8C), shielded from light, and must not be frozen.

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