USPTO Examiner KUCKLA ANNA GRACE - Art Unit 1626

Recent Applications

Detailed information about the 100 most recent patent applications.

Application NumberTitleFiling DateDisposal DateDispositionTime (months)Office ActionsRestrictionsInterviewAppeal
18912278MIRDAMETINIB TREATMENTOctober 2024December 2025Abandon1420NoNo
18780132Aminopyrimidine Derivatives as Cyclin-Dependent Kinase InhibitorsJuly 2024January 2025Allow600YesNo
18034296HDAC INHIBITOR SOLID STATE FORMSApril 2023March 2026Abandon3510NoNo
18033897PHARMACEUTICAL COMBINATION CONTAINING CAPSID PROTEIN INHIBITOR AND NUCLEOSIDE ANALOGApril 2023March 2026Abandon3510NoNo
18249783PHOSPHAPLATIN COMPOUNDS AS THERAPEUTIC AGENTS SELECTIVELY TARGETING HIGHLY GLYCOLYTIC TUMOR CELLS AND METHODS THEREOFApril 2023February 2026Abandon3401NoNo
18032387METHOD FOR PRODUCING DIIMINOPYRROLE COMPOUNDApril 2023February 2026Abandon3410NoNo
18192703ABIETANES AND METHODS OF MAKING AND USING THE SAMEMarch 2023December 2024Allow2110YesNo
18189380SULFONAMIDO DERIVATIVES AS CYCLIN-DEPENDENT KINASE 2 INHIBITORSMarch 2023February 2025Allow2301YesNo
18184335IKAROS ZINC FINGER FAMILY DEGRADERS AND USES THEREOFMarch 2023February 2025Allow2310NoNo
18044791ISOCHROMAN COMPOUNDMarch 2023July 2025Allow2900YesNo
181819652-AMINOTHIAZOLES DERIVATIVES AND METHOD OF PREPARATION THEREOF USING SUPER-PARAMAGNETIC IRON OXIDE NANOPARTICLES (SPIONS)March 2023January 2025Allow2311NoNo
18173426COMPOUNDS AS GLP-1R AGONISTSFebruary 2023March 2025Allow2511YesNo
18020827COMPOSITIONS AND METHODS FOR TREATING PROLIFERATIVE DISEASESFebruary 2023March 2026Abandon3701NoNo
18040667IMIDAZOTRIAZINE AND PYRROLOPYRIMIDINE DERIVATIVES AS KRAS G12C INHIBITORSFebruary 2023November 2025Allow3310NoNo
18004996Antiviral Heteroaryl Ketone DerivativesJanuary 2023January 2026Allow3610YesNo
18004722PYRAZOLONE FORMYL PEPTIDE 2 RECEPTOR AGONISTSJanuary 2023November 2025Allow3410NoNo
18013685METHODS OF TREATMENT FOR MELANOMADecember 2022January 2026Abandon3610NoNo
18084380BRAF DEGRADERSDecember 2022July 2025Allow3000YesNo
17925579ADAMANTANE AMIDES AND THIOAMIDES FOR THE TREATMENT OF EBOLAVIRUS INFECTIONNovember 2022December 2025Abandon3701NoNo
17998800INHIBITION OF ARENAVIRUSES BY COMBINATIONS OF APPROVED THERAPEUTIC DRUGSNovember 2022February 2026Abandon3910NoNo
17998546Piperazine Cyclic UreasNovember 2022June 2025Allow3100YesNo
17913870CATHEPSIN INHIBITORS FOR PREVENTING OR TREATING VIRAL INFECTIONSSeptember 2022December 2025Abandon3910NoNo
178952732,3-DISUBSTITUTED 1-ACYL-4-AMINO-1,2,3,4-TETRAHYDROQUINOLINE DERIVATIVES AND THEIR USE AS BROMODOMAIN INHIBITORSAugust 2022March 2025Allow3100NoNo
17798742NOVEL SALTS OF NILOTINIB AND POLYMORPHIC FORMS THEREOFAugust 2022October 2025Allow3910YesNo
17792757ISOINDOLINE DERIVATIVE, AND PHARMACEUTICAL COMPOSITION AND USE THEREOFJuly 2022November 2025Abandon4010NoNo
17758102PROCESS FOR THE PREPARATION OF PURINE DERIVATIVES EXHIBITING CDK INHIBITORY ACTIVITYJune 2022November 2025Abandon4110NoNo
17786295TETRAHYDROBENZO-QUINOLINE SULFONAMIDES DERIVATIVE COMPOUNDSJune 2022May 2025Allow3500YesNo
17783338NEW FYN AND VEGFR2 KINASE INHIBITORSJune 2022July 2025Allow3810NoNo
17663716COMPOUNDSMay 2022April 2025Allow3501YesNo
17777209COMBINATION DRUGMay 2022February 2026Abandon4520NoNo
17755780OPIOID RECEPTOR AGONIST, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL USE THEREOFMay 2022December 2025Allow4320NoNo
17767596PROCESS OF PREPARING (1R, 4R, 5S)-4-(2-CHLOROETHYL)-1-((S)-((S)-CYCLOHEX-2-EN-1-YL)(HYDROXY)METHYL)-5-METHYL-6-OXA-2-AZABICYCLO[3.2.0]HEPTANE-3,7-DIONE(SALINOSPORAMIDE A; MARIZOMIB)April 2022September 2025Abandon4210NoNo
17764658INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATIONMarch 2022January 2025Allow3400NoNo
17638741BENZIMIDAZOLE AND HYDROGENATED CARBAZOLE DERIVATIVES AS GPX4 INHIBITORSFebruary 2022May 2025Abandon3901NoNo
17637860PYRAZOLE DERIVATIVES AND USE THEREOFFebruary 2022January 2025Allow3400YesNo
17675917N2,N4-DIPHENYLPYRIMIDINE-2,4-DIAMINE DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT FOR PREVENTION OR TREATMENT OF CANCERFebruary 2022May 2025Abandon3910NoNo
176332095-HETEROARYL-PYRIDIN-2-AMINE COMPOUNDS AS NEUROPEPTIDE FF RECEPTOR ANTAGONISTSFebruary 2022May 2025Abandon4001NoNo
176321321H-[1, 2, 3]TRIAZOLO[4, 5-H] QUINAZOLINE COMPOUNDS ACTING AS PROTEIN KINASE INHIBITORSFebruary 2022January 2025Allow3610NoNo
17577949PHARMACEUTICAL FORMULATIONS, PROCESSES FOR PREPARATION, AND METHODS OF USEJanuary 2022June 2025Abandon4110NoNo
17626904PYRROMETHENE-BORON COMPLEX, COLOR CONVERSION COMPOSITION, COLOR CONVERSION FILM, LIGHT SOURCE UNIT, DISPLAY, AND ILLUMINATION DEVICEJanuary 2022January 2026Allow4921NoNo
17620782BICYCLIC HETEROCYCLIC COMPOUNDS AS INHIBITORS OF BCDIN3D ACTIVITYDecember 2021April 2025Abandon4001NoNo
17619367COMBINATION FOR THE TREATMENT OF INFECTIONS CAUSED BY MYCOPLASMA GENITALIUMDecember 2021January 2026Abandon4920NoNo
17618767INDAZOLE DERIVATIVE, PREPARATION METHOD THEREFOR, AND PHARMACEUTICAL APPLICATION THEREOFDecember 2021February 2025Allow3801YesNo
17615821PROSTAGLANDIN E2 RECEPTOR 4 ANTAGONISTS AND USES THEREOFDecember 2021May 2025Abandon4201NoNo
17614751VERY LONG CHAIN FATTY ACIDS FOR TREATMENT AND ALLEVIATION OF DISEASESNovember 2021January 2026Abandon4921NoNo
17613221MESYLATE SALT OF PARA-TOPOLIN, COMPOSITIONS CONTAINING SAID SALT AND USE THEREOFNovember 2021March 2025Allow4011YesNo
17595567DIETARY BUTYRATE AND ITS USESNovember 2021November 2025Abandon4820NoNo
17611527COMBINATION THERAPIES WITH IRE1 SMALL MOLECULE INHIBITORSNovember 2021January 2026Abandon5020NoNo
17609989SUBSTITUTED 1-AMINO-1H-IMIDAZOLE-5-CARBOXAMIDE AS BRUTON'S TYROSINE KINASE INHIBITORSNovember 2021January 2025Allow3801YesNo
17610037SMALL MOLECULE MODULATORS OF GUT BACTERIAL BILE ACID METABOLISMNovember 2021October 2025Allow4721NoNo
17608524PREPARATION FOR USE IN WEIGHT MANAGEMENT COMPRISING OMEGA-3 FATTY ACID SALTS AND BASIC AMINO ACIDSNovember 2021March 2025Abandon4010NoNo
17608459COMPOUNDS INHIBITING TDG ACTIVITYNovember 2021March 2025Abandon4001NoNo
17605808GINKGOLIDE B DERIVATIVE AND SALT THEREOF, PREPARATION METHOD THEREFOR AND USE THEREOFOctober 2021April 2025Allow4211YesNo
17604606METHODS OF TREATING NEUROCOGNITIVE DISORDERS, CHRONIC PAIN AND REDUCING INFLAMMATIONOctober 2021March 2025Allow4110YesNo
17604226COMBINATION WITH CHECKPOINT INHIBITORS TO TREAT CANCEROctober 2021December 2025Abandon5001NoNo

Appeals Overview

No appeal data available for this record. This may indicate that no appeals have been filed or decided for applications in this dataset.

Examiner KUCKLA, ANNA GRACE - Prosecution Strategy Guide

Executive Summary

Examiner KUCKLA, ANNA GRACE works in Art Unit 1626 and has examined 15 patent applications in our dataset. With an allowance rate of 40.0%, this examiner allows applications at a lower rate than most examiners at the USPTO. Applications typically reach final disposition in approximately 42 months.

Allowance Patterns

Examiner KUCKLA, ANNA GRACE's allowance rate of 40.0% places them in the 7% 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 KUCKLA, ANNA GRACE receive 0.93 office actions before reaching final disposition. This places the examiner in the 7% 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 KUCKLA, ANNA GRACE is 42 months. This places the examiner in the 18% 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 +90.0% benefit to allowance rate for applications examined by KUCKLA, ANNA GRACE. This interview benefit is in the 100% 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.

After-Final Amendment Practice

This examiner enters after-final amendments leading to allowance in 100.0% of cases where such amendments are filed. This entry rate is in the 98% 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.

Examiner Cooperation and Flexibility

Examiner's Amendments: This examiner makes examiner's amendments in 0.0% of allowed cases (in the 1% 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 0.0% of allowed cases (in the 1% percentile). This examiner rarely issues Quayle actions compared to other examiners. Allowances typically come directly without a separate action for formal matters.

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.
  • 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.