Product image of Nintedanib (Nintedanib Esylate) supplied by GNH India

Nintedanib

Active Ingredient:
Nintedanib Esylate
Origin:
EU

Nintedanib (Nintedanib Esylate)

Nintedanib, the active ingredient in Nintedanib, is a tyrosine kinase inhibitor presented as a capsule for oral use. It treats idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and is used in combination therapy for non‑small cell lung cancer in appropriate patients.

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

Manufacturer / TM Owner

Sandoz Pharmaceuticals D.D.

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Indications & Clinical Uses

Nintedanib is indicated for fibrotic lung diseases and as part of combination therapy for certain lung cancers.

  • Idiopathic pulmonary fibrosis (IPF): slows disease progression and reduces decline in lung function.
  • Systemic sclerosis‑associated interstitial lung disease (SSc‑ILD): improves forced vital capacity and delays worsening.
  • Non‑small cell lung cancer (NSCLC) in combination with docetaxel: enhances overall survival and response rates in previously treated patients.

How It Works

  • Nintedanib inhibits multiple receptor tyrosine kinases—including vascular endothelial growth factor receptors (VEGFR 1‑3), platelet‑derived growth factor receptors (PDGFR‑α/β), and fibroblast growth factor receptors (FGFR 1‑3). By blocking these pathways, it reduces fibroblast proliferation, migration, and transformation, and also exerts anti‑angiogenic effects that contribute to its antifibrotic and antineoplastic activity.

Side Effects

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

Common Side Effects

  • Diarrhea: frequent, may be mild to moderate.
  • Nausea: occasional gastrointestinal upset.
  • Vomiting: occasional.
  • Elevated liver enzymes (ALT/AST): mild elevations.

Serious or Rare Side Effects

  • Hepatotoxicity: severe liver injury requiring monitoring.
  • Bleeding events: increased risk of hemorrhage, especially with anticoagulants.
  • Cardiovascular events: rare cases of myocardial infarction or arterial thromboembolism.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Liver function monitoring: assess ALT/AST before treatment and periodically during therapy.
  • Gastrointestinal management: advise patients to stay hydrated and report severe diarrhea.
  • Drug interactions: avoid concomitant use with strong CYP3A4 inhibitors without dose adjustment.
  • Pregnancy risk: contraindicated in pregnancy; ensure effective contraception.
  • Bleeding risk: assess bleeding history and avoid use with anticoagulants unless necessary.
  • Store at ambient temperature: keep capsules below 25°C in original packaging, protect from moisture.

Avoid Interactions

Nintedanib has notable interactions that require attention.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase nintedanib exposure.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): heightened bleeding risk.
  • P‑glycoprotein inhibitors (e.g., verapamil): can raise plasma levels.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inducers (e.g., rifampicin): may reduce efficacy.
  • Antiplatelet agents (e.g., aspirin, clopidogrel): monitor for bleeding.
  • NSAIDs: increase gastrointestinal adverse events.

Frequently Asked Questions

Nintedanib is prescribed for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and as part of combination therapy with docetaxel for previously treated non‑small cell lung cancer. It targets fibrotic processes in the lung and helps control tumor‑related angiogenesis.

Nintedanib blocks several receptor tyrosine kinases—VEGFR, PDGFR, and FGFR—thereby inhibiting fibroblast activation and angiogenesis. This dual antifibrotic and anti‑angiogenic action reduces scar tissue formation in the lungs and limits blood vessel growth that supports tumor progression.

The specific dose and dosing schedule of Nintedanib are determined by the prescribing clinician based on the patient’s condition, renal and hepatic function, and concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Nintedanib is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should not be used during pregnancy, and effective contraception is required for women of child‑bearing potential. Breastfeeding is not recommended while taking the medication.

To order Nintedanib, submit an enquiry on the product page at gnhindia.com with 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 any cold‑chain requirements), and necessary import documentation.

The primary alternative for idiopathic pulmonary fibrosis is pirfenidone, another antifibrotic agent. While both slow disease progression, Nintedanib’s broader kinase inhibition also offers anti‑angiogenic benefits useful in certain lung cancers. Choice between them depends on patient tolerance, comorbidities, and physician assessment.

Nintedanib capsules should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture and direct sunlight. Do not refrigerate or freeze the product.

Nintedanib is taken orally as a capsule, usually with food to lessen gastrointestinal discomfort. Patients should swallow the capsule whole with water and follow the dosing schedule prescribed by their healthcare provider.

The most serious risks include liver injury (elevated transaminases or hepatitis), severe bleeding events, and rare cardiovascular complications such as myocardial infarction or arterial thromboembolism. Regular monitoring of liver function and vigilance for signs of bleeding are essential.

Nintedanib is contraindicated in pregnant women, patients with severe hepatic impairment, uncontrolled bleeding disorders, and those receiving strong CYP3A4 inhibitors without dose adjustment. Clinicians should also exercise caution in patients with a history of cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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