Product image of Grafalon (Anti-T Lymphocyte Immunoglobulin For Human Use, Rabbit) supplied by GNH India

Grafalon

Active Ingredient:
Anti-T Lymphocyte Immunoglobulin For Human Use, Rabbit
Origin:
EU

Grafalon (Anti-T Lymphocyte Immunoglobulin For Human Use, Rabbit)

Grafalon is an injectable solution containing anti‑T‑lymphocyte immunoglobulin (rabbit) for human use, supplied in a standard strength as a prescription‑only product in the European Union. It belongs to the immunosuppressant drug class and is administered intravenously to modulate the immune response in specific transplant settings.

Manufacturer / TM Owner

Neovii Biotech Gmbh

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Indications & Clinical Uses

Grafalon is indicated for use in transplant medicine where T‑cell mediated immunity must be controlled. It is employed in both solid‑organ and hematopoietic stem cell transplantation protocols.

  • Prevention of acute rejection following kidney, liver, heart, or lung transplantation.
  • Induction therapy to facilitate engraftment in hematopoietic stem cell transplantation.
  • Part of conditioning regimens prior to allogeneic stem cell transplant.
  • Adjunct to other immunosuppressive agents in multi‑drug transplant protocols.
  • Situations requiring rapid T‑cell depletion to reduce immune activation.

Side Effects

Grafalon may cause a range of adverse reactions, some of which are expected and others that require immediate medical attention.

Common

  • Fever and chills during or shortly after infusion.
  • Nausea, vomiting, or abdominal discomfort.
  • Headache or mild dizziness.
  • Transient hypertension or blood pressure fluctuations.
  • Mild leukopenia or lymphopenia.
  • Injection‑site reactions such as erythema or swelling.

Serious

  • Severe infections due to profound immunosuppression.
  • Cytokine release syndrome presenting with hypotension and respiratory distress.
  • Serum sickness or type III hypersensitivity reactions.
  • Anaphylaxis or severe allergic response.
  • Pulmonary edema or acute respiratory distress syndrome.
  • Renal impairment or acute kidney injury.

Precautions & Warnings

When prescribing Grafalon, clinicians should evaluate patient‑specific risk factors and monitor closely for complications.

  • Screen for active infections (viral, bacterial, fungal) before initiation.
  • Monitor complete blood counts, renal function, and liver enzymes regularly.
  • Avoid use in patients with known hypersensitivity to rabbit proteins.
  • Use with caution in pregnant or breastfeeding individuals; discuss potential risks.
  • Ensure appropriate vaccination status; avoid live vaccines during treatment.
  • Adjust dosing in patients with pre‑existing renal insufficiency.
  • Provide prophylactic antimicrobial therapy as recommended by transplant protocols.

Avoid Interactions

Grafalon can interact with other agents that affect immune function or hemostasis.

Avoid

  • Live attenuated vaccines during and for several weeks after therapy.
  • Concurrent use of other T‑cell depleting antibodies without specialist guidance.

Use with caution

  • Calcineurin inhibitors (e.g., tacrolimus, cyclosporine) due to additive nephrotoxicity.
  • Antimetabolites such as mycophenolate mofetil or azathioprine.
  • Antiviral prophylaxis agents (e.g., ganciclovir) requiring dose adjustments.
  • Anticoagulants or antiplatelet drugs because of potential bleeding risk.
  • Corticosteroids, which may amplify immunosuppressive effects.

Frequently Asked Questions

Grafalon contains polyclonal rabbit antibodies that bind to human T‑lymphocytes, leading to their depletion and modulation of the immune response, which helps prevent graft rejection.

Grafalon is used in solid‑organ transplants such as kidney, liver, heart, and lung, as well as in hematopoietic stem cell transplantation for induction therapy.

Grafalon is supplied as an injectable solution and is administered intravenously under the supervision of a qualified healthcare professional.

The safety of Grafalon during pregnancy has not been established; clinicians should weigh potential benefits against risks and discuss options with the patient.

Patients should have regular monitoring of complete blood counts, renal and liver function tests, and clinical assessment for signs of infection or hypersensitivity.

Live vaccines are generally avoided during Grafalon treatment and for several weeks afterward because of the heightened risk of infection.

Common side effects include fever, chills, nausea, headache, transient hypertension, mild leukopenia, and injection‑site reactions.

Serious reactions such as severe infection, cytokine release syndrome, serum sickness, anaphylaxis, pulmonary edema, or acute kidney injury require urgent evaluation.

Grafalon is often used as part of a multi‑drug regimen; however, combinations with other T‑cell depleting agents should be managed by a transplant specialist.

Dose adjustments and close monitoring of renal function are recommended for patients with pre‑existing kidney disease.

The duration of T‑cell depletion varies; clinicians typically monitor lymphocyte counts and adjust therapy based on individual response.

Prophylactic antibiotics, antivirals, or antifungals may be prescribed according to transplant protocol to reduce infection risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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