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Gavreto | European Medicines Agency (EMA)

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Overview

The marketing authorisation for Gavreto has been withdrawn at the request of the marketing-authorisation holder.

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Product information

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eesti keel (ET)
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français (FR)
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hrvatski (HR)
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íslenska (IS)
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italiano (IT)
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latviešu valoda (LV)
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lietuvių kalba (LT)
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Latest procedure affecting product information:
T/0021

17/07/2024

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This medicine’s product information is available in all official EU languages.
Select ‘available languages’ to access the language you need.

 

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

български (BG)
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español (ES)
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čeština (CS)
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dansk (DA)
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eesti keel (ET)
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ελληνικά (EL)
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français (FR)
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hrvatski (HR)
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íslenska (IS)
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italiano (IT)
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latviešu valoda (LV)
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lietuvių kalba (LT)
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magyar (HU)
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Nederlands (NL)
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norsk (NO)
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polski (PL)
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português (PT)
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română (RO)
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slovenčina (SK)
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slovenščina (SL)
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Suomi (FI)
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svenska (SV)
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Product details

Name of medicine

Gavreto

Active substance

pralsetinib

International non-proprietary name (INN) or common name

pralsetinib

Therapeutic area (MeSH)

Carcinoma, Non-Small-Cell Lung

Anatomical therapeutic chemical (ATC) code

L01EX23

Pharmacotherapeutic group

Antineoplastic agents

Therapeutic indication

Gavreto is indicated as monotherapy for the treatment of adult patients with rearranged during transfection (RET) fusion-positive advanced non-small cell lung cancer (NSCLC) not previously treated with a RET inhibitor.

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