Product image of Opdualag (Nivolumab, Relatlimab) supplied by GNH India

Opdualag

Active Ingredient:
Nivolumab, Relatlimab
Origin:
EU

Opdualag (Nivolumab, Relatlimab)

nivolumab and relatlimab, the active ingredient in Opdualag, is a PD‑1/LAG‑3 inhibitor presented as an intravenous infusion for intravenous use. It treats unresectable or metastatic melanoma in adult patients, providing dual checkpoint blockade to enhance anti‑tumor immunity.

GNH India supplies Opdualag as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide. The company adheres to stringent quality standards and provides cold‑chain logistics for biologic products. Clients include hospital pharmacies, cancer treatment centers, and national health systems seeking reliable access to advanced immunotherapies.

Manufacturer / TM Owner

Bristol-Myers Squibb Pharma Eeig

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

  • Opdualag is indicated for melanoma, acting through dual PD‑1 and LAG‑3 checkpoint inhibition.
  • Unresectable melanoma: provides disease control in patients whose tumors cannot be surgically removed.
  • Metastatic melanoma: extends overall survival in patients with distant spread.
  • Advanced melanoma: offers a therapeutic option after prior systemic therapy failure.

How It Works

  • Opdualag combines nivolumab, a monoclonal antibody that blocks the PD‑1 receptor on T cells, with relatlimab, which inhibits the LAG‑3 receptor. By simultaneously disabling these two immune checkpoints, the drug restores T‑cell activation and proliferation, enhancing the immune system’s ability to recognize and destroy tumor cells.

Side Effects

Opdualag may cause a range of immune‑related adverse reactions, which are categorized by frequency.

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Rash or pruritus: skin irritation or itching.
  • Diarrhea: loose stools that may require supportive care.
  • Nausea: feeling of sickness often managed with anti‑emetics.

Serious or Rare Side Effects

  • Immune‑mediated pneumonitis: inflammation of lung tissue that can impair breathing.
  • Colitis: severe inflammation of the colon leading to abdominal pain and diarrhea.
  • Hepatitis: liver inflammation that may elevate transaminases.
  • Endocrinopathies: disorders of thyroid, pituitary, or adrenal glands requiring hormone replacement.

Precautions & Warnings

  • Before initiating Opdualag, clinicians should observe several precautionary measures to minimize risk.
  • Baseline organ assessment: evaluate liver, kidney, and pulmonary function prior to therapy.
  • Monitor for immune‑related events: conduct regular clinical and laboratory surveillance for signs of inflammation.
  • Avoid live vaccines: patients should not receive live attenuated vaccines during treatment.
  • Caution in autoimmune disease: assess risk‑benefit in patients with pre‑existing autoimmune conditions.
  • Discontinue for severe toxicity: hold or stop therapy if grade 3‑4 adverse events occur.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Opdualag can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Concurrent immune checkpoint inhibitors: may amplify immune‑related toxicity.
  • Systemic immunosuppressants (e.g., high‑dose steroids): can reduce therapeutic efficacy.
  • Live vaccines: increase risk of infection due to immune modulation.

Moderate Interactions (Monitor Closely)

  • Corticosteroids used for other conditions: monitor for additive immunosuppression.
  • Anticoagulants: watch for bleeding if immune‑mediated thrombocytopenia develops.
  • Hormone replacement therapies: adjust dosing if endocrine dysfunction occurs.

Frequently Asked Questions

Opdualag is a cancer immunotherapy indicated for the treatment of adult patients with unresectable or metastatic melanoma. It works by blocking two immune checkpoints, PD‑1 and LAG‑3, to enhance the body’s immune response against melanoma cells.

Nivolumab binds to the PD‑1 receptor on T cells, preventing its interaction with PD‑L1 and restoring T‑cell activity. Relatlimab blocks the LAG‑3 receptor, another inhibitory pathway. Together they provide dual checkpoint inhibition, leading to a stronger anti‑tumor immune response.

The dosing regimen for Opdualag is determined by the prescribing oncologist based on the patient’s clinical condition, body weight, and treatment protocol. Specific dose amounts and infusion schedules are outlined in the product’s prescribing information and should not be altered without medical guidance.

Safety data for Opdualag in pregnant or nursing women are limited. Because the drug can affect the immune system, it is generally not recommended during pregnancy or breastfeeding unless the potential benefit justifies the potential risk. Consultation with a specialist is essential.

To order Opdualag, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details, and necessary import documentation.

Compared with single‑agent PD‑1 inhibitors such as pembrolizumab, Opdualag adds LAG‑3 blockade, offering a broader checkpoint inhibition. Clinical studies have shown improved response rates and survival in certain patient groups, though safety profiles remain similar, requiring monitoring for immune‑related adverse events.

Opdualag must be stored refrigerated at 2‑8 °C. It should be kept in its original packaging, protected from light, and must not be frozen or shaken. During transport, a validated cold‑chain system is required to maintain product stability.

Opdualag is given as an intravenous infusion. The infusion is administered by a qualified healthcare professional in a clinical setting, typically over a period of 30‑60 minutes, with patients monitored for infusion‑related reactions.

The most serious risks include immune‑mediated pneumonitis, colitis, hepatitis, endocrinopathies (such as thyroiditis), and severe skin reactions. Early detection through regular clinical and laboratory assessments is crucial, and prompt management may involve treatment interruption or corticosteroids.

Opdualag is contraindicated in patients with active uncontrolled autoimmune diseases, those receiving other immune checkpoint inhibitors, and individuals with known hypersensitivity to either nivolumab or relatlimab. Caution is also advised for organ‑transplant recipients due to the risk of graft rejection.

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.