
Brian A. Whiteman
Examiner (ID: 2464)
| Most Active Art Unit | 1635 |
| Art Unit(s) | 1635, 1674, 1636, 1633 |
| Total Applications | 1737 |
| Issued Applications | 917 |
| Pending Applications | 262 |
| Abandoned Applications | 606 |
Applications
| Application number | Title of the application | Filing Date | Status |
|---|---|---|---|
Array
(
[id] => 18117730
[patent_doc_number] => 11549112
[patent_country] => US
[patent_kind] => B1
[patent_issue_date] => 2023-01-10
[patent_title] => RNAi agents for inhibiting expression of xanthine dehydrogenase (XDH), pharmaceutical compositions thereof, and methods of use
[patent_app_type] => utility
[patent_app_number] => 17/748779
[patent_app_country] => US
[patent_app_date] => 2022-05-19
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Array
(
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[patent_doc_number] => 20230068339
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[patent_kind] => A1
[patent_issue_date] => 2023-03-02
[patent_title] => APOLIPOPROTEIN C3 (APOC3) iRNA COMPOSITIONS AND METHODS OF USE THEREOF
[patent_app_type] => utility
[patent_app_number] => 17/741550
[patent_app_country] => US
[patent_app_date] => 2022-05-11
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Array
(
[id] => 17960327
[patent_doc_number] => 20220340907
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[patent_kind] => A1
[patent_issue_date] => 2022-10-27
[patent_title] => OLIGONUCLEOTIDES FOR TREATMENT OF ANGIOPOIETIN LIKE 4 (ANGPTL4) RELATED DISEASES
[patent_app_type] => utility
[patent_app_number] => 17/736928
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[patent_app_date] => 2022-05-04
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Array
(
[id] => 18552428
[patent_doc_number] => 20230250437
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[patent_kind] => A1
[patent_issue_date] => 2023-08-10
[patent_title] => OLIGONUCLEOTIDE PROBES AND USES THEREOF
[patent_app_type] => utility
[patent_app_number] => 17/727263
[patent_app_country] => US
[patent_app_date] => 2022-04-22
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Array
(
[id] => 18020977
[patent_doc_number] => 20220372476
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[patent_kind] => A1
[patent_issue_date] => 2022-11-24
[patent_title] => DYNAMIC PHARMACOKINETIC-MODIFYING ANCHORS
[patent_app_type] => utility
[patent_app_number] => 17/725102
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[patent_app_date] => 2022-04-20
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/725102 | Dynamic pharmacokinetic-modifying anchors | Apr 19, 2022 | Issued |
Array
(
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[patent_title] => BISPECIFIC APTAMER FOR TREATING CANCER
[patent_app_type] => utility
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/719189 | BISPECIFIC APTAMER FOR TREATING CANCER | Apr 11, 2022 | Abandoned |
Array
(
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[patent_title] => Methods and Systems of Molecular Recording by Crispr-Cas System
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/717283 | Methods and Systems of Molecular Recording by Crispr-Cas System | Apr 10, 2022 | Pending |
Array
(
[id] => 18036560
[patent_doc_number] => 20220380775
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[patent_kind] => A1
[patent_issue_date] => 2022-12-01
[patent_title] => ORGANIC COMPOSITIONS TO TREAT HSF1-RELATED DISEASES
[patent_app_type] => utility
[patent_app_number] => 17/714272
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/714272 | Organic compositions to treat HSF1-related diseases | Apr 5, 2022 | Issued |
Array
(
[id] => 17928481
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[patent_title] => Targeting Technology to Selectively Express mRNAs in Cardiomyocytes While Avoiding Stimulation of Cardiac Fibroblasts
[patent_app_type] => utility
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/711125 | Targeting technology to selectively express mRNAs in cardiomyocytes while avoiding stimulation of cardiac fibroblasts | Mar 31, 2022 | Issued |
Array
(
[id] => 18036557
[patent_doc_number] => 20220380772
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[patent_issue_date] => 2022-12-01
[patent_title] => RNA INTERFERENCE MEDIATED INHIBITION OF PROLYL HYDROXYLASE DOMAIN 2 (PHD2) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (SINA)
[patent_app_type] => utility
[patent_app_number] => 17/711114
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/711114 | RNA interference mediated inhibition of prolyl hydroxylase domain 2 (PHD2) gene expression using short interfering nucleic acid (siNA) | Mar 31, 2022 | Issued |
Array
(
[id] => 19701731
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[patent_title] => Compositions and processes for targeted delivery, expression and modulation of coding ribonucleic acids in tissue
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Array
(
[id] => 17735042
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Array
(
[id] => 18871399
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[patent_title] => DNA aptamer, pharmaceutical composition comprising same, method for inhibiting catalytic ability of TXNDC5, and method for preventing or treating organ fibrosis
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Array
(
[id] => 17897394
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Array
(
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Array
(
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[patent_title] => ANTISENSE OLIGONUCLEOTIDES FOR THE TREATMENT OF LEBER CONGENITAL AMAUROSIS
[patent_app_type] => utility
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/678433 | Antisense oligonucleotides for the treatment of Leber congenital amaurosis | Feb 22, 2022 | Issued |
Array
(
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Array
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Array
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Array
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[patent_title] => O-METHYL RICH FULLY STABILIZED OLIGONUCLEOTIDES
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[rel_patent_id] =>[rel_patent_doc_number] =>) 17/580269 | O-methyl rich fully stabilized oligonucleotides | Jan 19, 2022 | Issued |