Product image of Kyprolis (Carfilzomib) supplied by GNH India

Kyprolis

Active Ingredient:
Carfilzomib
Origin:
EU

Kyprolis (Carfilzomib)

Carfilzomib, the active ingredient in Kyprolis, is a proteasome inhibitor presented as an intravenous solution for intravenous use. It is indicated for the treatment of relapsed or refractory multiple myeloma in adult patients who have received prior therapy.

GNH India supplies Kyprolis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Amgen Europe B.V.

1
Pack/s
This product is added to your enquiry list

Request a Quote

Please fill out the form below and our team will get back to you shortly with pricing and further information.

A minimum order value applies. Our team will confirm the exact amount or quantity after reviewing your requirements.

Indications & Clinical Uses

  • Kyprolis (carfilzomib) is used in the management of plasma cell malignancies, specifically multiple myeloma.
  • Multiple myeloma (relapsed or refractory): Improves disease control and prolongs progression‑free survival in patients who have received prior treatment.
  • Multiple myeloma (post‑autologous stem cell transplant): Provides maintenance therapy to extend remission after transplant.
  • Multiple myeloma (combination therapy): Used with dexamethasone and/or lenalidomide to enhance overall response rates.

How It Works

  • Carfilzomib irreversibly binds to the N‑terminal β5 subunit of the 20S proteasome, selectively inhibiting its chymotrypsin‑like activity. This blockade prevents degradation of polyubiquitinated proteins, causing accumulation of misfolded proteins, endoplasmic reticulum stress and activation of apoptotic pathways in malignant plasma cells.

Side Effects

Kyprolis may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Nausea: mild to moderate upset stomach.
  • Anemia: reduced red blood cell count leading to weakness.
  • Thrombocytopenia: lowered platelet count increasing bleeding risk.

Serious or Rare Side Effects

  • Cardiac toxicity: heart failure or reduced ejection fraction.
  • Pulmonary hypertension: elevated pressure in lung arteries.
  • Severe infusion reactions: hypotension, dyspnea, or anaphylaxis.
  • Renal failure: acute kidney injury requiring monitoring.

Precautions & Warnings

  • Before initiating Kyprolis, clinicians should assess several safety parameters.
  • Cardiac monitoring: evaluate baseline cardiac function and watch for signs of heart failure.
  • Hematologic monitoring: perform regular complete blood counts to detect anemia, neutropenia or thrombocytopenia.
  • Infection risk: monitor for febrile neutropenia and treat infections promptly.
  • Liver function: check hepatic enzymes before and during therapy.
  • Pregnancy and lactation: avoid use; safety not established and contraception is advised.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Kyprolis can interact with several medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may markedly decrease carfilzomib levels.
  • Concurrent proteasome inhibitors: risk of additive toxicity.
  • Anticoagulants (e.g., warfarin): increased bleeding risk.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole): may raise carfilzomib exposure.
  • Drugs that prolong QT interval: monitor ECG for arrhythmias.
  • Nephrotoxic agents (e.g., cisplatin): observe renal function closely.

Frequently Asked Questions

Kyprolis is indicated for the treatment of adult patients with relapsed or refractory multiple myeloma, including those who have previously undergone stem cell transplantation or received other anti‑myeloma therapies.

Carfilzomib irreversibly inhibits the 20S proteasome’s chymotrypsin‑like activity, leading to accumulation of polyubiquitinated proteins, cellular stress and programmed cell death specifically in malignant plasma cells.

The dosing regimen for Kyprolis is individualized by the prescribing oncologist based on the patient’s clinical status, prior therapies and tolerance. Exact dose and infusion schedule are determined by the treating physician.

Safety of Kyprolis during pregnancy or lactation has not been established. It is generally contraindicated in pregnant or nursing women; effective contraception is recommended for women of child‑bearing potential.

To order Kyprolis, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

The primary alternative is bortezomib, another proteasome inhibitor. Carfilzomib provides irreversible inhibition and may have a different toxicity profile, with lower rates of peripheral neuropathy but higher potential for cardiac events, while bortezomib is reversible and often associated with neuropathy.

Kyprolis must be stored refrigerated between 2 °C and 8 °C, protected from light, and should never be frozen or shaken. Prior to administration, the solution should be inspected for particulate matter and used within the time frame recommended by the manufacturer.

Kyprolis is given as an intravenous infusion over a specified period, typically on a weekly or bi‑weekly schedule as directed by the oncologist. The infusion rate and duration are adjusted according to patient tolerance and clinical response.

Serious risks include cardiac toxicity such as heart failure or reduced ejection fraction, pulmonary hypertension, severe infusion‑related reactions, and acute renal failure. Patients should be monitored closely for signs of these events throughout treatment.

Kyprolis is contraindicated in patients with known hypersensitivity to carfilzomib or any component of the formulation, those with uncontrolled cardiac disease, severe hepatic impairment, and in pregnant or nursing women. Clinicians should evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

Disclaimer

At GNH India, we aim to provide information that is expert-reviewed, accurate, and reliable. However, all content on this platform is intended for general informational purposes only and does not constitute professional medical advice, diagnosis, or treatment. While efforts are made to maintain accuracy and currency, the information may contain errors, omissions, or may not reflect the latest developments. Always consult a qualified healthcare professional regarding any medical concerns.

All product names, brand names, trademarks and registered trademarks displayed on this website are the property of their respective owners. This website and its operator are not affiliated with, endorsed by, or authorized by any such trade mark owners unless expressly stated. Any reference to product names or trademarks is made solely for descriptive and informational purposes. No commercial relationship, sponsorship, approval, or association with any trademark owner should be inferred. Information provided herein does not constitute promotion, advertising, or an offer for sale of any medicinal product and is intended solely for general informational purposes.

All trademarks and brand names displayed on this website are used strictly in accordance with the provisions of the Trade Marks Act, 1999, specifically Sections 30 and 30(1) governing fair use. Trademark ownership has been accurately attributed under the "Manufacturer/ TM Owner" section in compliance with statutory requirements.

Ordering Process

Simple, Secure, and Seamless

Learn how our streamlined ordering process guarantees fast, compliant, and reliable access to essential medicines worldwide.

Quote request form

01

Submit Quote Request Form

Tell us what medications you need by filling out our simple form and uploading a valid document.

Price estimate review

02

We Review & Send Estimate

Our licensed pharmacists will verify your details and provide you with a detailed cost estimate.

Secure payment

03

Confirm & Make Payment

Discuss any queries, approve the estimate, and complete your payment.

Worldwide delivery

04

Get Delivered

Your medicines, safely packed and delivered to your door or nearest airport — hassle-free.

Quality You Can Trust

Our internationally recognized certifications underscore our commitment to safety, quality, and excellence.