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

Nintedanib Eignapharma

Active Ingredient:
Nintedanib
Origin:
EU

Nintedanib Eignapharma (Nintedanib)

Nintedanib, the active ingredient in Nintedanib Eignapharma, is a tyrosine kinase inhibitor presented as an oral tablet for oral use. It is indicated for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease and non‑small cell lung cancer in combination with docetaxel.
GNH India supplies Nintedanib Eignapharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Eignapharma Slu

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Indications & Clinical Uses

Nintedanib Eignapharma acts on multiple receptor tyrosine kinases that drive fibrotic and oncogenic pathways. It is clinically employed for the following conditions:

  • Idiopathic pulmonary fibrosis: slows disease progression and reduces decline in lung function.
  • Systemic sclerosis‑associated interstitial lung disease: limits fibrotic remodeling and preserves respiratory capacity.
  • Non‑small cell lung cancer (in combination with docetaxel): enhances anti‑tumour efficacy and improves survival outcomes.

How It Works

  • Nintedanib inhibits the intracellular kinase activity of 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 limit tumour vascularisation and fibrotic tissue development.

Side Effects

Nintedanib may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Diarrhoea: frequent loose stools, often early in treatment.
  • Decreased appetite: reduced desire to eat.
  • Abdominal pain: discomfort or cramps in the stomach area.
  • Elevated liver enzymes: mild increases in ALT/AST.

Serious or Rare Side Effects

  • Hepatic failure: signs of severe liver injury.
  • Severe bleeding: gastrointestinal or intracranial haemorrhage.
  • Arterial thromboembolism: clot formation in arteries.
  • Severe hypertension: markedly high blood pressure.
  • Perforation of the gastrointestinal tract: rare but life‑threatening.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate several safety aspects.

  • Liver monitoring: perform baseline and periodic liver function tests.
  • Bleeding risk: assess for anticoagulant use or bleeding disorders.
  • Cardiovascular assessment: check blood pressure and history of arterial events.
  • Pregnancy avoidance: drug is contraindicated in pregnancy (Category D).
  • Hepatic impairment dose adjustment: consider reduced exposure in severe liver disease.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Nintedanib can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase nintedanib exposure.
  • Potent P‑gp inhibitors (e.g., verapamil): can raise plasma concentrations.
  • Concurrent use of other anti‑angiogenic agents: heightens risk of bleeding and hypertension.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors or inducers (e.g., fluconazole, rifampicin): may modestly alter drug levels.
  • Antacids or proton‑pump inhibitors: could affect absorption if taken simultaneously.
  • Diuretics: monitor electrolytes and renal function.
  • Anticoagulants (e.g., warfarin): observe for increased bleeding tendency.

Frequently Asked Questions

Nintedanib Eignapharma is prescribed for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and for non‑small cell lung cancer when given together with docetaxel. In each case it targets pathways that drive fibrosis or tumour angiogenesis, helping to slow disease progression.

The drug blocks several receptor tyrosine kinases—VEGFR, PDGFR and FGFR—preventing their activation. This inhibition reduces fibroblast growth and migration, limits extracellular matrix deposition, and also impairs the formation of new blood vessels that support tumour growth.

Dosing is individualized and must be set by a qualified prescriber based on the specific indication, patient characteristics and any concomitant therapies. The product label provides detailed guidance, and clinicians adjust the regimen as needed.

Nintedanib is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should not be used during pregnancy, and breastfeeding is not recommended because the drug may pass into milk. Women of child‑bearing potential should use effective contraception.

To place an order, 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, shipping details (including any cold‑chain needs) and required import documentation.

The primary alternative for fibrotic lung disease is pirfenidone, another antifibrotic agent. Nintedanib targets a broader range of tyrosine kinases, offering a different safety profile—more gastrointestinal events but less photosensitivity than pirfenidone. Choice depends on patient tolerance, comorbidities and physician judgment.

Store the product at temperatures below 25 °C in its original container, protecting it from moisture and direct sunlight. Do not expose the tablets to excessive heat or humidity, and keep them out of reach of children.

The medication is taken orally, usually with food to lessen gastrointestinal discomfort. Patients should swallow the tablet whole with a full glass of water and follow the dosing schedule prescribed by their healthcare provider.

Clinicians and patients should be alert for signs of severe liver injury (jaundice, dark urine), major bleeding events (vomiting blood, unusual bruising), arterial thromboembolism (sudden chest pain, stroke symptoms), and uncontrolled hypertension. Prompt medical evaluation is essential if any of these occur.

The drug is contraindicated in pregnant women, patients with severe hepatic impairment, and individuals with known hypersensitivity to nintedanib or any of its excipients. Caution is also advised for patients with a history of bleeding disorders or uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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