USPTO Examiner WILSON JERICA KATLYNN - Art Unit 1621

Recent Applications

Detailed information about the 100 most recent patent applications.

Application NumberTitleFiling DateDisposal DateDispositionTime (months)Office ActionsRestrictionsInterviewAppeal
19029638Compounds and Their Use for Treatment of HemoglobinopathiesJanuary 2025July 2025Allow611NoNo
18968101SUBSTITUTED PHENYL OXAZOLONE COMPOUNDSDecember 2024April 2025Allow510NoNo
18943269NASAL COMPOSITIONS COMPRISING ALCAFTADINENovember 2024September 2025Abandon1020NoNo
18914691ARYL-1,2,3-TRIAZOLE COMPOUNDS, PHARMACEUTICAL COMPOSITION THEREOF AND METHOD FOR TREATMENT OF BREAST CANCEROctober 2024January 2025Allow310NoNo
18676679POLYMORPHS OF PHENYL PYRROLE AMINOGUANDIUM SALTSMay 2024January 2025Allow821YesNo
18663952PRMT5 INHIBITORS AND USES THEREOFMay 2024February 2025Allow911NoNo
18646687THIOAMIDE DERIVATIVE AND PREPARATION METHOD AND APPLICATION THEREOFApril 2024October 2024Allow610NoNo
18634599IMIDAZOTRIAZINE THIOBENZAMIDE DERIVATIVE, AND PREPARATION METHOD AND APPLICATION THEREOFApril 2024November 2024Allow710NoNo
18131183LYSYL OXIDASE INHIBITORS FOR TREATING MYELOID MALIGNANCIESApril 2023October 2024Allow1820NoNo
18191283METHOD OF TREATMENT USING SUBSTITUTED PYRAZOLO[1,5-A] PYRIMIDINE COMPOUNDSMarch 2023February 2026Allow3510NoNo
18187789PYRIMID-2-YL-PYRAZOLE COMPOUNDS AS IRAK INHIBITORSMarch 2023April 2025Allow2421YesNo
18182234INHIBITORS OF NITRIC OXIDE SYNTHASES (NOS), PHARMACEUTICAL PRODUCTS THEREOF, AND METHODS THEREOFMarch 2023January 2025Allow2321YesNo
18042497COMBINATION THERAPIES WITH OLIG2 INHIBITORSFebruary 2023February 2026Abandon3610NoNo
18107164SOLID FORMS OF A PARP14 INHIBITORFebruary 2023March 2026Abandon3701NoNo
18161609PYRIDAZINONE-BASED COMPOUNDS AS AXL, C-MET, AND MER INHIBITORS AND METHODS OF USE THEREOFJanuary 2023May 2024Abandon1510NoNo
18015592COMPOSITIONS COMPRISING GARDOS CHANNEL ANTAGONISTS AND THEIR USESJanuary 2023February 2026Abandon3701NoNo
18014764PYRIDAZINYL AMINO DERIVATIVES AS ALK5 INHIBITORSJanuary 2023July 2025Allow3100NoNo
18014664COMBINATION OF AN ALPHA2-ADRENOCEPTOR SUBTYPE C (ALPHA-2C) ANTAGONIST WITH A TASK1/3 CHANNEL BLOCKER FOR THE TREATMENT OF SLEEP APNEAJanuary 2023March 2026Abandon3801NoNo
18014178ATR INHIBITORS AND USES THEREOFJanuary 2023February 2026Abandon3710NoNo
18013721PYRROLIDINE AMIDE DERIVATIVE SALT AND USE THEREOFDecember 2022January 2026Allow3710NoNo
18145618DEUBIQUITINASE INHIBITORS AND METHODS OF USE THEREOFDecember 2022February 2025Allow2621NoNo
17992961CRYSTALLINE FORMS OF SOLVATES OF TRYPTOPHAN DERIVATIVES, COMPOSITIONS COMPRISING THEM AND USES THEREOFNovember 2022January 2026Allow3720NoNo
17959466METHOD AND COMPOSITION FOR MIMICKING BIOLOGICAL BENEFITS OF CALORIC RESTRICTIONOctober 2022November 2025Abandon3850YesNo
17906127NERVE CELL DEGENERATION INHIBITORSeptember 2022January 2026Abandon4010NoNo
17897388CO-CRYSTALSAugust 2022October 2024Allow2520YesNo
17821500POLYMORPHS OF PHENYL PYRROLE AMINOGUANDIUM SALTSAugust 2022February 2026Allow4211NoNo
17800184COMPOUNDSAugust 2022January 2026Abandon4101NoNo
17816950PENTADECANOYLCARNITINE FOR TREATMENT OF CONDITIONS RELATED TO THE QUALITY OF AGING AND LONGEVITYAugust 2022December 2024Allow2921NoNo
17792249COMPOSITIONS COMPRISING AMINO ACIDS FOR PREVENTION AND/OR TREATMENT OF CANCERJuly 2022January 2026Allow4210NoNo
17860096Additive for Food, Drink and Pharmaceutical Products to Improve Health and Well-BeingJuly 2022January 2026Abandon4210NoNo
17857706COMPOUNDS AS GCN2 INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOFJuly 2022August 2024Allow2511YesNo
17789321COMPOUNDS FOR THE TREATMENT OF MYELOFIBROSISJune 2022December 2025Abandon4210NoNo
17846693CANNABIDIOL-BASED TOPICAL REMEDYJune 2022January 2025Abandon3120NoNo
17843205COMPOSITIONS PROVIDING SLOW RELEASE OF CAFFEINE AND BEVERAGES COMPRISING THE SAMEJune 2022January 2026Abandon4321NoYes
17782632TREATMENT FOR ACUTE MYELOID LEUKEMIA OR MYELODYSPLASTIC SYNDROMEJune 2022September 2025Allow3910NoNo
17776040ANTIMALARIAL AGENTSMay 2022March 2025Allow3400YesNo
17740275METHOD FOR CONTINUOUSLY PREPARING N,N-BIS(2,2,6,6-TETRAMETHYL-4-PIPERIDYL)-1,6-HEXAMETHYLENEDIAMINEMay 2022May 2024Allow2410NoNo
17774662Application of Boron Dipyrromethene Derivatives in Anti-Tumor and Anti-Bacterial TherapyMay 2022March 2025Allow3520YesNo
17772334FIVE-MEMBERED HETEROCYCLIC OXOCARBOXYLIC ACID COMPOUND AND MEDICAL USE THEREOFApril 2022January 2026Abandon4510NoNo
17755292ACID ADDITION SALT OF RORy REGULATORApril 2022November 2025Abandon4310NoNo
17640294Androstane Derivatives with Activity as Pure or Predominantly Pure Stimulators of SERCA2a for the Treatment of Heart Failure.March 2022August 2025Allow4110YesNo
17625649STABLE ORAL COMPOSITION OF CYCLOPHOSPHAMIDEJanuary 2022July 2025Allow4210NoNo
17542830METHODS OF MEDICAL TREATMENT WITH SUR1-TRPM4 CHANNEL INHIBITORSDecember 2021December 2025Abandon4820NoNo
176153631,3,4-OXADIAZOLE HOMOPHTHALIMIDE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAMENovember 2021June 2025Allow4210YesNo
17610867SUSTAINED-RELEASE MICROGEL OINTMENTS WITH HIGH DRUG LOADING AND PREPARATION METHODS AND USES THEREOFNovember 2021February 2025Allow4010NoNo
17519922Benzoquinoline Inhibitors of Vesicular Monoamine Transporter 2November 2021April 2025Abandon4210NoNo
17606319CATECHOLAMINE PRODRUGS FOR USE IN THE TREATMENT OF PARKINSON'S DISEASEOctober 2021April 2025Allow4110NoNo
17496433TREATMENT OF CANCER WITH TOR KINASE INHIBITORSOctober 2021November 2025Abandon5020NoNo
17496276Process of Manufacturing a Stable, Ready to Use Infusion Bag for an Oxidation Sensitive FormulationOctober 2021September 2025Abandon4710NoNo
17602057HEXAHYDRO-1H-PYRAZINO[1,2-A]PYRAZINE COMPOUNDS FOR THE TREATMENT OF AUTOIMMUNE DISEASEOctober 2021January 2025Allow4010NoNo
17593474A DBAIT MOLECULE IN COMBINATION WITH KINASE INHIBITOR FOR THE TREATMENT OF CANCERSeptember 2021August 2025Abandon4710NoNo
17438262APPLICATIONS OF IMINOSTILBENE IN TERMS OF PREVENTING AND TREATING CARDIAC CEREBRAL ISCHEMIA/REPERFUSION INJURYSeptember 2021July 2025Abandon4620NoNo
17435276METHODS OF TREATING CANCER WITH FARNESYLTRANSFERASE INHIBITORSAugust 2021March 2025Abandon4310NoNo
17461988TREATMENT WITH P2X3 MODULATORSAugust 2021August 2025Allow4730YesNo
17461325FATTY ACID ANALOGS AND THEIR USE IN THE TREATMENT OF COGNITIVE IMPAIRMENT, BEHAVIORAL CONDITIONS, AND CHRONIC PAINAugust 2021May 2025Allow4420YesNo
17045409COMPOSITION FOR PREVENTING AND TREATMENT OF STROKEAugust 2021December 2024Abandon5010NoNo
17430721BIFUNCTIONAL COMPOUNDS FOR DEGRADING BTK VIA UBIQUITIN PROTEOSOME PATHWAYAugust 2021August 2025Allow4820YesNo
17430060TRIAMTERENE OR NOLATREXED FOR USE IN THE TREATMENT OF PHENYLKETONURIAAugust 2021December 2024Allow4010NoNo
17430240COMPOSITIONS COMPRISING AMINO ACIDS FOR USE AND TREATMENT OF CENTRAL NERVOUS SYSTEM INJURIESAugust 2021October 2025Allow5040YesNo
17429575PHARMACEUTICAL COMPOSITION FOR PREVENTION OR TREATMENT OF ACIDOSISAugust 2021May 2025Abandon4510NoNo
17428917METHODS FOR TREATING CUTANEOUS AGINGAugust 2021January 2026Abandon5420NoYes
17310181CANNABIDIOL AND/OR DERIVATIVES THEREOF FOR USE IN THE TREATMENT OF MITOCHONDRIAL DISEASESJuly 2021April 2025Allow4520NoNo
17421741DIHYDROOROTATE DEHYDROGENASE INHIBITORSJuly 2021April 2025Abandon4510NoNo
17415085AGENT FOR IMPROVING INFERTILITY, RECURRENT MISCARRIAGE, AND STATE OF PREGNANCYJune 2021June 2025Abandon4820NoNo
17414404ORAL THERAPY USING 6,8-BIS-BENZYLTHIO-OCTANOIC ACIDJune 2021June 2025Abandon4820NoNo
17413346METHOD FOR PRODUCING REFINED PRODUCT OF PEAR JUICEJune 2021February 2025Abandon4501NoNo
17312898STABLE FORMULATIONS OF ANESTHETICS AND ASSOCIATED DOSAGE FORMSJune 2021November 2024Abandon4110NoNo
17344830KINASE INHIBITORS AND METHODS OF USE THEREOFJune 2021April 2025Allow4621YesNo
17341817KINASE INHIBITORS AND METHODS FOR MAKING AND USINGJune 2021September 2024Abandon4001NoNo
17341158SOLID DISPERSIONS CONTAINING AN APOPTOSIS-INDUCING AGENTJune 2021October 2024Abandon4110NoNo
17340082BICYCLIC SULFONES AND SULFOXIDES AND METHODS OF USE THEREOFJune 2021February 2025Allow4411NoNo
17298198ELACESTRANT IN COMBINATION WITH ABEMACICLIB IN WOMEN WITH BREAST CANCERMay 2021June 2025Abandon4820NoNo
17294353INHIBITORS OF ARG1 AND/OR ARG2May 2021October 2024Allow4110NoNo
17292677MICROMOLECULAR COMPOUND SPECIFICALLYDEGRADING TAU PROTEIN, AND APPLICATION THEREOFMay 2021October 2024Allow4110NoNo
17292511SUBSTITUTED AMINO TRIAZOLOPYRIMIDINE AND AMINO TRIAZOLOPYRAZINE ADENOSINE RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITIONS AND THEIR USEMay 2021May 2025Allow4811YesNo
17292480COMBINATION OF A MCL-1 INHIBITOR AND MIDOSTAURIN, USES AND PHARMACEUTICAL COMPOSITIONS THEREOFMay 2021November 2024Abandon4311NoNo
17292528HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF EPILEPSYMay 2021March 2025Allow4621NoNo
17313885EPINEPHRINE SPRAY FORMULATIONSMay 2021January 2025Allow4410YesNo
17245240GASTRIC CANCER TREATMENTSApril 2021September 2024Abandon4111NoNo
17289406TRIFLUOROMETHYL-SUBSTITUTED SULFONAMIDE AS BCL-2-SELECTIVE INHIBITORApril 2021February 2025Allow4521NoNo
17288063UPADACITINIB CRYSTAL FORM AND PREPARATION METHOD THEREFOR AND USE THEREOFApril 2021August 2024Abandon4001NoNo
17286904PPAR delta ACTIVATORApril 2021December 2024Allow4420NoNo
17286932SYNTHESIS OUTSIDE HIGH AND LOW TEMPERATURE EQUILIBRIUM BY SPRAY FLASH SYNTHESISApril 2021November 2024Allow4310YesNo
17285780PROCESS FOR PRODUCING ETHYLENE OXIDE BY GAS-PHASE OXIDATION OF ETHYLENEApril 2021August 2024Allow4010NoNo
17231168Novel Phenyl DerivativesApril 2021October 2024Abandon4201NoNo
17285791TRANSCRIPTIONAL ENHANCED ASSOCIATE DOMAIN (TEAD) TRANSCRIPTION FACTOR INHIBITORS AND USES THEREOFApril 2021March 2026Allow5941NoNo
17285414COMPOSITIONS AND METHODS FOR SUPPRESSING AND/OR TREATING A GROWTH RELATED DISEASE AND/OR A CLINICAL CONDITION THEREOFApril 2021August 2024Abandon4010NoNo
17285180COMPOUND AS TGF-beta R1 INHIBITOR AND APPLICATION THEREOFApril 2021July 2024Abandon3901NoNo
17229036SUBSTITUTED PYRIDINE AND PYRIMIDINES AND THEIR USE AS GLUN2B RECEPTOR MODULATORSApril 2021September 2024Abandon4111NoNo
17224025SHP2 INHIBITOR COMPOSITIONS FOR USE IN TREATING CANCERApril 2021August 2024Abandon4001NoNo
17281745EGFR INHIBITORS FOR TREATING KERATODERMASMarch 2021August 2025Allow5240NoNo
172803533-AZABICYCLO[3,1,1]HEPTANE DERIVATIVE AND PHARMACEUTICAL COMPOSITION INCLUDING SAMEMarch 2021July 2024Allow3910NoNo
17278017NOVEL SULFONAMIDE DERIVATIVE WITH FUSED PYRIMIDINE SKELETON, HAVING EPIDERMAL GROWTH FACTOR RECEPTOR MUTATION INHIBITORY EFFECTMarch 2021January 2025Allow4621NoNo
17276459COMBINATION THERAPY FOR TREATING BLOOD CANCERMarch 2021May 2024Allow3810NoNo
17275604COMBINATION OF PARP INHIBITOR AND BRD4 INHIBITOR FOR THE TREATMENT OF CANCERMarch 2021June 2024Abandon3910NoNo
17275450IMMUNOMODULATORS, COMPOSITIONS AND METHODS THERE OFMarch 2021June 2024Allow4011NoNo
17275462COMBINATION THERAPY FOR THE TREATMENT OF ESTROGEN-RECEPTOR POSITIVE BREAST CANCERMarch 2021December 2025Abandon5840YesNo
17274736NOVEL INHIBITORS OF GUANOSINE MONOPHOSPHATE SYNTHETASE AS THERAPEUTIC AGENTSMarch 2021October 2024Allow4411YesNo
17273646METHODS OF TREATING CYTOKINE RELEASE SYNDROMEMarch 2021June 2024Abandon3901NoNo
17268042BIOMARKERS FOR CANCER THERAPYFebruary 2021August 2024Allow4211YesNo

Appeals Overview

This analysis examines appeal outcomes and the strategic value of filing appeals for examiner WILSON, JERICA KATLYNN.

Strategic Value of Filing an Appeal

Total Appeal Filings
1
Allowed After Appeal Filing
0
(0.0%)
Not Allowed After Appeal Filing
1
(100.0%)
Filing Benefit Percentile
0.2%
Lower than average

Understanding Appeal Filing Strategy

Filing a Notice of Appeal can sometimes lead to allowance even before the appeal is fully briefed or decided by the PTAB. This occurs when the examiner or their supervisor reconsiders the rejection during the mandatory appeal conference (MPEP § 1207.01) after the appeal is filed.

In this dataset, 0.0% of applications that filed an appeal were subsequently allowed. This appeal filing benefit rate is in the bottom 25% across the USPTO, indicating that filing appeals is less effective here than in most other areas.

Strategic Recommendations

Filing a Notice of Appeal shows limited benefit. Consider other strategies like interviews or amendments before appealing.

Examiner WILSON, JERICA KATLYNN - Prosecution Strategy Guide

Executive Summary

Examiner WILSON, JERICA KATLYNN works in Art Unit 1621 and has examined 63 patent applications in our dataset. With an allowance rate of 52.4%, this examiner allows applications at a lower rate than most examiners at the USPTO. Applications typically reach final disposition in approximately 44 months.

Allowance Patterns

Examiner WILSON, JERICA KATLYNN's allowance rate of 52.4% places them in the 14% percentile among all USPTO examiners. This examiner is less likely to allow applications than most examiners at the USPTO.

Office Action Patterns

On average, applications examined by WILSON, JERICA KATLYNN receive 1.35 office actions before reaching final disposition. This places the examiner in the 20% percentile for office actions issued. This examiner issues significantly fewer office actions than most examiners.

Prosecution Timeline

The median time to disposition (half-life) for applications examined by WILSON, JERICA KATLYNN is 44 months. This places the examiner in the 14% percentile for prosecution speed. Applications take longer to reach final disposition with this examiner compared to most others.

Interview Effectiveness

Conducting an examiner interview provides a +52.0% benefit to allowance rate for applications examined by WILSON, JERICA KATLYNN. This interview benefit is in the 94% percentile among all examiners. Recommendation: Interviews are highly effective with this examiner and should be strongly considered as a prosecution strategy. Per MPEP § 713.10, interviews are available at any time before the Notice of Allowance is mailed or jurisdiction transfers to the PTAB.

Request for Continued Examination (RCE) Effectiveness

When applicants file an RCE with this examiner, 38.2% of applications are subsequently allowed. This success rate is in the 87% percentile among all examiners. Strategic Insight: RCEs are highly effective with this examiner compared to others. If you receive a final rejection, filing an RCE with substantive amendments or arguments has a strong likelihood of success.

After-Final Amendment Practice

This examiner enters after-final amendments leading to allowance in 62.5% of cases where such amendments are filed. This entry rate is in the 87% percentile among all examiners. Strategic Recommendation: This examiner is highly receptive to after-final amendments compared to other examiners. Per MPEP § 714.12, after-final amendments may be entered "under justifiable circumstances." Consider filing after-final amendments with a clear showing of allowability rather than immediately filing an RCE, as this examiner frequently enters such amendments.

Petition Practice

When applicants file petitions regarding this examiner's actions, 76.9% are granted (fully or in part). This grant rate is in the 82% percentile among all examiners. Strategic Note: Petitions are frequently granted regarding this examiner's actions compared to other examiners. Per MPEP § 1002.02(c), various examiner actions are petitionable to the Technology Center Director, including prematureness of final rejection, refusal to enter amendments, and requirement for information. If you believe an examiner action is improper, consider filing a petition.

Examiner Cooperation and Flexibility

Examiner's Amendments: This examiner makes examiner's amendments in 0.0% of allowed cases (in the 0% percentile). This examiner rarely makes examiner's amendments compared to other examiners. You should expect to make all necessary claim amendments yourself through formal amendment practice.

Quayle Actions: This examiner issues Ex Parte Quayle actions in 24.2% of allowed cases (in the 94% percentile). Per MPEP § 714.14, a Quayle action indicates that all claims are allowable but formal matters remain. This examiner frequently uses Quayle actions compared to other examiners, which is a positive indicator that once substantive issues are resolved, allowance follows quickly.

Prosecution Strategy Recommendations

Based on the statistical analysis of this examiner's prosecution patterns, here are tailored strategic recommendations:

  • Prepare for rigorous examination: With a below-average allowance rate, ensure your application has strong written description and enablement support. Consider filing a continuation if you need to add new matter.
  • Prioritize examiner interviews: Interviews are highly effective with this examiner. Request an interview after the first office action to clarify issues and potentially expedite allowance.
  • Consider after-final amendments: This examiner frequently enters after-final amendments. If you can clearly overcome rejections with claim amendments, file an after-final amendment before resorting to an RCE.
  • RCEs are effective: This examiner has a high allowance rate after RCE compared to others. If you receive a final rejection and have substantive amendments or arguments, an RCE is likely to be successful.
  • Plan for extended prosecution: Applications take longer than average with this examiner. Factor this into your continuation strategy and client communications.

Relevant MPEP Sections for Prosecution Strategy

  • MPEP § 713.10: Examiner interviews - available before Notice of Allowance or transfer to PTAB
  • MPEP § 714.12: After-final amendments - may be entered "under justifiable circumstances"
  • MPEP § 1002.02(c): Petitionable matters to Technology Center Director
  • MPEP § 1004: Actions requiring primary examiner signature (allowances, final rejections, examiner's answers)
  • MPEP § 1207.01: Appeal conferences - mandatory for all appeals
  • MPEP § 1214.07: Reopening prosecution after appeal

Important Disclaimer

Not Legal Advice: The information provided in this report is for informational purposes only and does not constitute legal advice. You should consult with a qualified patent attorney or agent for advice specific to your situation.

No Guarantees: We do not provide any guarantees as to the accuracy, completeness, or timeliness of the statistics presented above. Patent prosecution statistics are derived from publicly available USPTO data and are subject to data quality limitations, processing errors, and changes in USPTO practices over time.

Limitation of Liability: Under no circumstances will IronCrow AI be liable for any outcome, decision, or action resulting from your reliance on the statistics, analysis, or recommendations presented in this report. Past prosecution patterns do not guarantee future results.

Use at Your Own Risk: While we strive to provide accurate and useful prosecution statistics, you should independently verify any information that is material to your prosecution strategy and use your professional judgment in all patent prosecution matters.