Product image of Gloftrinid (Bortezomib) supplied by GNH India

Gloftrinid

Active Ingredient:
Bortezomib
Origin:
EU

Gloftrinid (Bortezomib)

Gloftrinid is a prescription medication whose active ingredient is bortezomib, a proteasome inhibitor used in oncology. It is supplied in an injectable form for intravenous or subcutaneous administration, though specific strength and dosage form details are not disclosed. Marketed within the European Union, Gloftrinid belongs to the antineoplastic therapeutic class and is intended for use under medical supervision. Patients receive it in clinical settings where dosing is individualized by oncologists.

Manufacturer / TM Owner

Alkaloid-Int D.O.O.

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Indications & Clinical Uses

Gloftrinid is indicated for the treatment of certain hematologic malignancies, primarily in patients who have not responded adequately to prior therapy. It is prescribed as part of combination regimens to improve disease control and prolong survival.

  • Treatment of newly diagnosed multiple myeloma in combination with dexamethasone and immunomodulatory agents.
  • Therapy for relapsed or refractory multiple myeloma after prior lines of treatment.
  • Management of mantle cell lymphoma in patients unsuitable for stem‑cell transplantation.
  • Use in clinical trials evaluating bortezomib‑based regimens for other B‑cell malignancies.

Side Effects

Like other proteasome inhibitors, Gloftrinid may cause a range of adverse effects that vary in frequency and severity.

Common

  • Fatigue or weakness.
  • Nausea, vomiting, or loss of appetite.
  • Diarrhea or constipation.
  • Peripheral neuropathy (tingling or numbness in hands/feet).
  • Low blood cell counts (anemia, neutropenia, thrombocytopenia).

Serious

  • Severe allergic reactions (anaphylaxis, rash, fever).
  • Cardiac arrhythmias or heart failure.
  • Pulmonary toxicity (interstitial lung disease).

Precautions & Warnings

Before initiating Gloftrinid, clinicians assess patient-specific factors and monitor for conditions that could increase the risk of complications.

  • Baseline and periodic evaluation of blood counts and liver function tests.
  • Assessment for pre‑existing peripheral neuropathy; dose adjustments may be needed.
  • Screening for hepatitis B and C, as reactivation can occur.
  • Caution in patients with cardiac disease or uncontrolled hypertension.
  • Avoid use during pregnancy; discuss contraception with women of childbearing potential.
  • Monitor for signs of infection, especially febrile neutropenia.
  • Adjust dosing in patients with severe renal impairment.

Avoid Interactions

Gloftrinid can interact with other medicines, influencing its efficacy or safety profile, so careful review of concomitant drugs is essential.

Avoid

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine) that may reduce bortezomib exposure.
  • Live vaccines during treatment due to immunosuppression.

Use with caution

  • Anticoagulants (warfarin, DOACs) because of increased bleeding risk.
  • Other neurotoxic agents (e.g., vincristine) that may exacerbate peripheral neuropathy.
  • Concomitant use of other proteasome inhibitors or investigational agents.

Frequently Asked Questions

Gloftrinid is a prescription antineoplastic agent whose active ingredient is bortezomib, a reversible proteasome inhibitor used to treat certain blood cancers.

It is commonly prescribed for multiple myeloma and mantle cell lymphoma, either as first‑line therapy or after disease relapse.

Gloftrinid is given by a healthcare professional as an intravenous or subcutaneous injection; the exact dosing schedule is determined by the treating oncologist.

Gloftrinid is not recommended for use during pregnancy, and women of childbearing potential should discuss reliable contraception with their physician.

Regular monitoring of complete blood counts, liver function tests, and assessment for peripheral neuropathy are standard practice during treatment.

Common side effects include fatigue, nausea, diarrhea or constipation, peripheral neuropathy, and reductions in blood cell counts such as anemia or neutropenia.

Serious reactions can include severe allergic responses, cardiac arrhythmias or heart failure, and pulmonary toxicity such as interstitial lung disease.

Live vaccines should be avoided because Gloftrinid can suppress the immune system, increasing the risk of infection.

Strong CYP3A4 inducers, such as rifampin or carbamazepine, should be avoided as they may lower bortezomib levels and reduce effectiveness.

Bortezomib reversibly inhibits the 26S proteasome, leading to accumulation of polyubiquitinated proteins and triggering apoptosis in malignant cells.

Dose adjustments may be required for patients with severe renal impairment; the treating physician will evaluate kidney function before prescribing.

Yes, Gloftrinid is often combined with dexamethasone and immunomodulatory drugs as part of a multi‑agent regimen, but the combination should be managed by an oncologist.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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