Difference between revisions of "Talazoparib (Talzenna)"

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==Mechanism of action==
 
==Mechanism of action==
 
PARP inhibitor
 
PARP inhibitor
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*[https://www.guidetopharmacology.org/GRAC/LigandDisplayForward?ligandId=8313 IUPHAR/BPS]
  
 
==Diseases for which it is used==
 
==Diseases for which it is used==
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==History of changes in EMA indication==
 
==History of changes in EMA indication==
 
*2019-06-20: Initial authorization as Talzenna. Talzenna is indicated as monotherapy for the treatment of adult patients with germline BRCA1/2 mutations, who have HER2-negative locally advanced or metastatic [[breast cancer]]. Patients should have been previously treated with an anthracycline and/or a taxane in the (neo)adjuvant, locally advanced or metastatic setting unless patients were not suitable for these treatments. Patients with hormone receptor (HR)-positive breast cancer should have been treated with a prior endocrine-based therapy, or be considered unsuitable for endocrine-based therapy. ''(Based on EMBRACA)''
 
*2019-06-20: Initial authorization as Talzenna. Talzenna is indicated as monotherapy for the treatment of adult patients with germline BRCA1/2 mutations, who have HER2-negative locally advanced or metastatic [[breast cancer]]. Patients should have been previously treated with an anthracycline and/or a taxane in the (neo)adjuvant, locally advanced or metastatic setting unless patients were not suitable for these treatments. Patients with hormone receptor (HR)-positive breast cancer should have been treated with a prior endocrine-based therapy, or be considered unsuitable for endocrine-based therapy. ''(Based on EMBRACA)''
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*2023-11-09: CHMP recommends new marketing authorisation - Talzenna is indicated in combination with enzalutamide for the treatment of adult patients with metastatic castration-resistant [[prostate cancer]] (mCRPC) in whom chemotherapy is not clinically indicated.
  
 
==Also known as==
 
==Also known as==
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[[Category:Mutation-specific medications]]
 
[[Category:Mutation-specific medications]]
  
[[Category:PARP inhibitors]]
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[[Category:PARP1 inhibitors]]
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[[Category:PARP2 inhibitors]]
  
 
[[Category:Breast cancer medications]]
 
[[Category:Breast cancer medications]]

Revision as of 18:14, 19 November 2023

Mechanism of action

PARP inhibitor

Diseases for which it is used

History of changes in FDA indication

  • 2018-10-16: Initial approval for patients with deleterious or suspected deleterious germline BRCA-mutated (gBRCAm), HER2-negative locally advanced or metastatic breast cancer. (Based on EMBRACA)
  • 2023-06-20: Approved with enzalutamide for homologous recombination repair (HRR) gene-mutated metastatic castration-resistant prostate cancer (mCRPC). (Based on TALAPRO-2)

History of changes in EMA indication

  • 2019-06-20: Initial authorization as Talzenna. Talzenna is indicated as monotherapy for the treatment of adult patients with germline BRCA1/2 mutations, who have HER2-negative locally advanced or metastatic breast cancer. Patients should have been previously treated with an anthracycline and/or a taxane in the (neo)adjuvant, locally advanced or metastatic setting unless patients were not suitable for these treatments. Patients with hormone receptor (HR)-positive breast cancer should have been treated with a prior endocrine-based therapy, or be considered unsuitable for endocrine-based therapy. (Based on EMBRACA)
  • 2023-11-09: CHMP recommends new marketing authorisation - Talzenna is indicated in combination with enzalutamide for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) in whom chemotherapy is not clinically indicated.

Also known as

  • Code name: BMN-673
  • Brand name: Talzenna