Product image of Gloftrinid (Bortezomib) supplied by GNH India

Gloftrinid

Active Ingredient:
Bortezomib
Origin:
EU

Gloftrinid (Bortezomib)

Gloftrinid is a prescription injectable medication that contains the active ingredient bortezomib. It is supplied as a sterile solution for intravenous or subcutaneous administration. The product is marketed in the European Union and belongs to the proteasome inhibitor class, used as an antineoplastic agent for certain blood cancers. Its formulation enables reversible inhibition of the 26S proteasome, leading to apoptosis of malignant cells.

Manufacturer / TM Owner

Alkaloid-Int D.O.O.

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Indications & Clinical Uses

Gloftrinid is indicated for the treatment of specific hematologic malignancies and is administered under the supervision of a qualified healthcare professional.

  • Treatment of newly diagnosed multiple myeloma in combination with other anti‑myeloma agents.
  • Therapy for relapsed or refractory multiple myeloma.
  • Management of mantle cell lymphoma, either as initial therapy or after disease progression.
  • Use as part of a multi‑drug regimen in clinical trials for other proteasome‑sensitive cancers.
  • May be considered for off‑label investigational use in selected proteasome‑dependent malignancies under strict clinical oversight.

Side Effects

Side effects of Gloftrinid vary in frequency and severity. Patients should be monitored regularly for both common and serious adverse reactions.

Common

  • Fatigue or generalized weakness.
  • Peripheral neuropathy, often presenting as tingling or numbness in the hands or feet.
  • Nausea, vomiting, or loss of appetite.
  • Diarrhea or constipation.
  • Low blood cell counts (anemia, neutropenia, thrombocytopenia).
  • Mild fever or flu‑like symptoms.

Serious

  • Severe peripheral neuropathy that interferes with daily activities.
  • Significant infections due to immune suppression.
  • Pulmonary complications such as dyspnea or interstitial lung disease.
  • Cardiac events including arrhythmias or heart failure.
  • Hepatic dysfunction indicated by elevated liver enzymes.
  • Severe hypersensitivity reactions, including anaphylaxis.

Precautions & Warnings

Gloftrinid requires careful patient assessment and ongoing monitoring to minimize risks.

  • Perform baseline and periodic complete blood counts to detect cytopenias.
  • Assess peripheral nerve function before each dose and adjust treatment if neuropathy worsens.
  • Monitor liver function tests regularly, especially in patients with pre‑existing hepatic disease.
  • Evaluate cardiac status in patients with known heart disease or risk factors.
  • Use caution in pregnant or breastfeeding women; discuss potential risks and benefits.
  • Avoid administration in patients with active uncontrolled infections.
  • Ensure proper injection technique to reduce injection‑site reactions.

Avoid Interactions

Gloftrinid may interact with other medications, affecting its safety or efficacy.

Avoid

  • Concurrent use of strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin) that may increase bortezomib exposure.
  • Live vaccines during treatment due to immunosuppression.
  • Other proteasome inhibitors, which could compound toxicity.

Use with caution

  • Anticoagulants, as thrombocytopenia may increase bleeding risk.
  • Immunosuppressive agents (e.g., corticosteroids, azathioprine) that may heighten infection risk.
  • Drugs that cause peripheral neuropathy (e.g., vincristine, taxanes) may exacerbate nerve damage.
  • Medications affecting hepatic metabolism, requiring dose adjustments based on liver function.

Frequently Asked Questions

Gloftrinid is a prescription injectable drug that contains the proteasome inhibitor bortezomib, used to treat certain blood cancers.

Gloftrinid is approved for the treatment of multiple myeloma and mantle cell lymphoma, either as first‑line therapy or for relapsed/refractory disease.

The medication is given by a healthcare professional as an intravenous or subcutaneous injection, following a dosing schedule determined by the treating physician.

Common adverse effects include fatigue, peripheral neuropathy, nausea, diarrhea, low blood cell counts, and mild fever or flu‑like symptoms.

Serious reactions can include severe neuropathy, significant infections, pulmonary complications, cardiac events, liver enzyme elevations, and severe allergic reactions.

Yes, routine complete blood counts and liver function tests are recommended to monitor for cytopenias and hepatic changes.

The safety of Gloftrinid in pregnancy has not been established; it should only be used if the potential benefits outweigh the risks and after consulting a healthcare provider.

Strong CYP3A4 inhibitors, live vaccines, and other proteasome inhibitors should be avoided because they can increase toxicity or reduce effectiveness.

Inform your doctor about any existing liver or heart conditions, current medications, history of neuropathy, and any infections or vaccinations you have received.

Bortezomib, the active ingredient, reversibly inhibits the 26S proteasome, causing accumulation of polyubiquitinated proteins and triggering apoptosis in malignant cells.

Coverage varies by country and individual health plans; patients should check with their national health service or private insurer for reimbursement details.

Yes, it is often used in combination with other anti‑myeloma drugs such as dexamethasone, lenalidomide, or cyclophosphamide, as directed by an oncologist.

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GNH India Pharmaceuticals Limited

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