Difference between revisions of "Pralsetinib (Gavreto)"

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(Created page with "==Mechanism of action== From the [NCI Drug Dictionary]: An orally bioavailable selective inhibitor of mutant forms of and fusion products involving the proto-oncogene receptor...")
 
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==Mechanism of action==
 
==Mechanism of action==
From the [NCI Drug Dictionary]: An orally bioavailable selective inhibitor of mutant forms of and fusion products involving the proto-oncogene receptor tyrosine kinase RET, with potential antineoplastic activity. Upon administration, BLU-667 binds to and targets various RET mutants and RET-containing fusion product.
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From the NCI Drug Dictionary: An orally bioavailable selective inhibitor of mutant forms of and fusion products involving the proto-oncogene receptor tyrosine kinase RET, with potential antineoplastic activity. Upon administration, BLU-667 binds to and targets various RET mutants and RET-containing fusion product.
  
 
==Diseases for which it is used==
 
==Diseases for which it is used==
 
*[[Non-small cell lung cancer, RET-positive|RET-positive NSCLC]]
 
*[[Non-small cell lung cancer, RET-positive|RET-positive NSCLC]]
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*[[Thyroid cancer, RET-positive]]
  
 
==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
*9/4/2020: Granted accelerated approval for adult patients with metastatic RET fusion-positive [[non-small cell lung cancer|non-small cell lung cancer (NSCLC)]]
 
*9/4/2020: Granted accelerated approval for adult patients with metastatic RET fusion-positive [[non-small cell lung cancer|non-small cell lung cancer (NSCLC)]]
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*12/1/2020: Approved for adult and pediatric patients 12 years of age and older with advanced or metastatic RET-mutant medullary [[thyroid cancer]] (MTC) who require systemic therapy.
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*12/1/2020: Approved for adult and pediatric patients 12 years of age and older with RET fusion-positive [[thyroid cancer]] who require systemic therapy and who are radioactive iodine-refractory (if radioactive iodine is appropriate).
  
 
==Also known as==
 
==Also known as==
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[[Category:Non-small cell lung cancer medications]]
 
[[Category:Non-small cell lung cancer medications]]
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[[Category:Thyroid cancer medications]]
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[[Category:FDA approved in 2020]]
 
[[Category:FDA approved in 2020]]

Revision as of 01:58, 2 December 2020

Mechanism of action

From the NCI Drug Dictionary: An orally bioavailable selective inhibitor of mutant forms of and fusion products involving the proto-oncogene receptor tyrosine kinase RET, with potential antineoplastic activity. Upon administration, BLU-667 binds to and targets various RET mutants and RET-containing fusion product.

Diseases for which it is used

History of changes in FDA indication

  • 9/4/2020: Granted accelerated approval for adult patients with metastatic RET fusion-positive non-small cell lung cancer (NSCLC)
  • 12/1/2020: Approved for adult and pediatric patients 12 years of age and older with advanced or metastatic RET-mutant medullary thyroid cancer (MTC) who require systemic therapy.
  • 12/1/2020: Approved for adult and pediatric patients 12 years of age and older with RET fusion-positive thyroid cancer who require systemic therapy and who are radioactive iodine-refractory (if radioactive iodine is appropriate).

Also known as

  • Code name: BLU-667
  • Brand name: Gavreto