US2022213553A1PendingUtilityA1

Prkc fusions

Assignee: BLUEPRINT MEDICINES CORPPriority: Jul 17, 2014Filed: Jan 21, 2022Published: Jul 7, 2022
Est. expiryJul 17, 2034(~8 yrs left)· nominal 20-yr term from priority
G01N 33/5752C12Q 2600/156C12Q 1/6886C12N 15/1138C07K 16/30G01N 33/57423
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Claims

Abstract

The invention provides PRKC gene fusions, PRKC fusion proteins, and fragments of those genes and polypeptides. The invention further provides methods of diagnosing and treating diseases or disorders associated with PRKC fusions, such as conditions mediated by aberrant PRKC expression or activity, or overexpression of PRKC.

Claims

exact text as granted — not AI-modified
1 - 81 . (canceled) 
     
     
         82 . A compound capable of specifically inhibiting a TRIM24:NTRK2, AFAP1:NTRK2, or PAN3:NTRK2 fusion, wherein the fusion results in aberrant activity or expression of NTRK2, or overexpression NTRK2, and wherein the compound is an antibody that specifically binds to a TRIM24:NTRK2, AFAP1:NTRK2, or PAN3:NTRK2 fusion protein or an RNA inhibitor that hybridizes under stringent conditions to a TRIM24:NTRK2, AFAP1:NTRK2, or PAN3:NTRK2 gene fusion. 
     
     
         83 . The compound of  claim 82 , wherein
 (a) the antibody specifically binds to:
 (i) a fragment of SEQ ID NO:3 comprising at least amino acids 665-674 of SEQ ID NO:3; 
 (ii) a fragment of SEQ ID NO:4 comprising at least amino acids 665-674 of SEQ ID NO:4; 
 (iii) a fragment of SEQ ID NO:6 comprising at least amino acids 544-553 of SEQ ID NO:6; or 
 (iv) a fragment of SEQ ID NO:8 comprising at least amino acids 138-147 of SEQ ID NO:8; and 
   (b) the RNA inhibitor hybridizes under stringent conditions to:
 (i) a fragment of SEQ ID NO:1 comprising at least nucleotides 2010-2019 of SEQ ID NO:1; 
 (ii) a fragment of SEQ ID NO:2 comprising at least nucleotides 2000-2009 of SEQ ID NO:2; 
 (iii) a fragment of SEQ ID NO:5 comprising at least nucleotides 1641-1650 of SEQ ID NO:5; or 
 (iv) a fragment of SEQ ID NO:7 comprising at least nucleotides 426-435 of SEQ ID NO:7. 
   
     
     
         84 . A method for detecting the presence of a PAN3:NTRK2 fusion in a patient, said method comprising:
 a) contacting a biological sample from the patient with an oligonucleotide that specifically binds to the fusion junction of the PAN3:NTRK2 fusion, and detecting binding between the PAN3:NTRK2 fusion and the olignucleotide; or   b) amplifying or sequencing a portion of a nucleic acid from the patient, and detecting the presence of a nucleotide sequence comprising at least the fusion junction of the PAN3:NTRK2 fusion.   
     
     
         85 . The method of  claim 84 , wherein the PAN3:NTRK2 fusion to be detected is a PAN3:NTRK2 gene fusion that comprises SEQ ID NO: 7, or a portion of SEQ ID NO: 7, wherein the portion encodes a nucleotide sequence comprising the fusion junction. 
     
     
         86 . The method of  claim 85 , wherein the oligonucleotide hybridizes to the fusion junction of the NTRK2 gene fusion under stringent conditions. 
     
     
         87 . The method of  claim 86 , wherein the oligonucleotide hybridizes under stringent conditions to
 a fragment of SEQ ID NO:7 comprising at least nucleotides 426-435 of SEQ ID NO:7.   
     
     
         88 - 90 . (canceled) 
     
     
         91 . The method of  claim 84 , further comprising administering to the patient a therapeutically effective amount of an NTRK2 inhibitor or an NTRK2 fusion inhibitor. 
     
     
         92 . The method of  claim 84 , wherein the patient is suffering from or susceptible to a cancer. 
     
     
         93 . The method of  claim 92 , wherein the cancer is lung adenocarcinoma, low grade glioma, squamous cell carcinoma, or head and neck squamous cell carcinoma.

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