USPTO Examiner SWARTWOUT BRIANNA KENDALL - Art Unit 1644

Recent Applications

Detailed information about the 100 most recent patent applications.

Application NumberTitleFiling DateDisposal DateDispositionTime (months)Office ActionsRestrictionsInterviewAppeal
18660591ANTI-SIRPalpha ANTIBODYMay 2024July 2025Allow1500YesNo
18426912FUSION PROTEIN AND NUCLEIC ACID ENCODING SEQUENCE THEREOF, AND USES OF THE SAMEJanuary 2024November 2024Allow1020YesNo
18420296ANTI-NGF ANTIBODIES AND USES THEREOFJanuary 2024March 2025Allow1421YesNo
18348173ANTI-NGF ANTIBODIES AND USES THEREOFJuly 2023May 2024Allow1011NoNo
18206552T CELL REGULATIONJune 2023March 2025Abandon2101NoNo
18125400METHODS FOR TREATING AND DIAGNOSING SYSTEMIC LUPUS ERYTHEMATOSUS BY MEASURING LEVELS OF BIOMARKERS, SUCH AS ERYTHROCYTE-BOUND C4D, B-LYMPHOCYTE-BOUND C4D, ANTI-SJOGREN'S SYNDROME TYPE B ANTIGEN, SCL-70 ANTIBODY, JO-1 ANTIBODY, AND ANTI-CENTROMERE PROTEIN B, IN SUBJECTS; IDENTIFYING SUBJECTS AS HAVING SYSTEMIC LUPUS ERYTHEMATOSUS BASED ON BIOMARKER LEVELS; AND TREATING SUBJECTS FOR SYSTEMIC LUPUS ERYTHEMATOSUSMarch 2023August 2025Abandon2931YesYes
18178278ANTI-PD1 ANTIBODIES AND METHODS OF USEMarch 2023November 2025Abandon3310NoNo
18152078ANTAGONISTIC ANTI-TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY POLYPEPTIDESJanuary 2023November 2025Abandon3410NoNo
18012580ANTIBODIES SPECIFICALLY RECOGNIZING C5A AND USES THEREOFDecember 2022November 2025Allow3501YesNo
17996866IMPROVED PEPTIDE VACCINEOctober 2022February 2026Abandon4010NoNo
17821706Nanobody Target GCC and Uses in Chimeric Antigen Receptor Cell TherapyAugust 2022December 2023Allow1601YesNo
17891020Compositions and Methods for Treatment and Prevention of Type 1 DiabetesAugust 2022May 2024Abandon2110NoNo
17818072CLDN18.2-TARGETING ANTIBODY, BISPECIFIC ANTIBODY AND USE THEREOFAugust 2022April 2025Allow3221NoNo
17817448ANTI-CD47 ANTIBODY AND USES THEREOFAugust 2022September 2023Allow1300YesNo
17854211TREATMENTS FOR DIFFUSE LARGE B-CELL LYMPHOMAJune 2022April 2024Abandon2210NoNo
17778689METHODS OF CANCER TREATMENT USING ANTI-OX40 ANTIBODIES IN COMBINATION WITH ANTI-TIM3 ANTIBODIESMay 2022December 2025Abandon4310NoNo
17767695T CELL RECEPTOR RECOGNISING KRAS MUTATION AND ENCODING SEQUENCE THEREOFApril 2022January 2026Allow4520NoNo
17642340USE OF HIGH-AFFINITY, LIGAND-BLOCKING, HUMANIZED ANTI-T-CELL IMMUNOGLOBULIN DOMAIN AND MUCIN DOMAIN-3 (TIM-3) IGG4 ANTIBODY FOR THE TREATMENT OF MYELOFIBROSISMarch 2022November 2025Abandon4410NoNo
17572611USE OF CD8-TARGETED VIRAL VECTORSJanuary 2022August 2025Abandon4321NoNo
17541273STABILIZED ARTIFICIAL IMMUNE COMPLEX ACTIVE IMMUNIZATION STRATEGY THAT SUPPORTS B CELL AND DENDRITIC CELL PROGRAMMING FOR CANCER IMMUNOTHERAPYDecember 2021July 2024Abandon3110NoNo
17616043Bispecific Antibody, Preparation Method Therefor and Application ThereofDecember 2021November 2025Allow4820YesNo
17615555ENGINEERING THE HINGE REGION TO DRIVE ANTIBODY DIMERIZATIONNovember 2021December 2025Allow4911NoNo
17607807BISPECIFIC ANTIBODY WITH DOUBLE HER2 SITES FOR TUMOR IMMUNOTHERAPYOctober 2021October 2025Abandon4810NoNo
17606744BISPECIFIC ANTIBODIES AGAINST PD-1 AND LAG-3October 2021September 2025Abandon4610NoNo
17489598MODULATORS OF CELL SURFACE PROTEIN INTERACTIONS AND METHODS AND COMPOSITIONS RELATED TO SAMESeptember 2021May 2025Abandon4301NoNo
17599716ANTI-INTEGRIN ANTIBODIES AND USES THEREOFSeptember 2021February 2026Abandon5211NoNo
17442638MONOCLONAL ANTIBODY AGAINST STIM1September 2021July 2025Allow4611YesNo
17425125NOVEL BISPECIFIC ANTIBODY MOLECULE AND BISPECIFIC ANTIBODY SIMULTANEOUSLY BINDING TO PD-L1 AND LAG-3July 2021February 2025Abandon4301NoNo
17425022CD31 COMPETITORS AND USES THEREOFJuly 2021February 2025Abandon4301NoNo
17413696ANTIBODIES THAT NEUTRALIZE HEPATITIS B VIRUS AND USES THEREOFJune 2021December 2024Allow4210YesNo
17413269ANTI-IL-27 ANTIBODIES AND USES THEREOFJune 2021March 2025Allow4511YesNo
17312630NOVEL POLYPEPTIDESJune 2021April 2025Abandon4611NoNo
17312847ANTI-TIM-3 ANTIBODIES AND USES THEREOFJune 2021March 2025Abandon4510NoNo
17312522NOVEL POLYPEPTIDESJune 2021January 2026Allow5521YesNo
17341201BORRELIA BURGDORFERI PEPTIDOGLYCAN AS A DIAGNOSTIC AND TARGET FOR THERAPEUTIC INTERVENTION OF LYME DISEASE-RELATED PATHOLOGIESJune 2021September 2025Allow5221YesNo
17298381FULLY HUMANIZED ANTI-GITR ANTIBODY AND PREPARATION METHOD THEREFORMay 2021November 2024Abandon4101NoNo
17297421ANTIBODIES SPECIFICALLY RECOGNIZING GRANULOCYTE-MACROPHAGE COLONY STIMULATING FACTOR RECEPTOR ALPHA AND USES THEREOFMay 2021July 2025Allow5021YesNo
17297386HUMANIZED ANTI-HUMAN OX40 MONOCLONAL ANTIBODY, PREPARATION METHOD THEREFOR AND USE THEREOFMay 2021November 2024Allow4110YesNo
17297333MARROW INFILTRATING LYMPHOCYTES (MILs) EXPRESSING CHIMERIC ANTIGEN RECEPTORS (CAR), METHOD OF MANUFACTURING SAME, AND METHOD OF USING IN THERAPYMay 2021August 2024Abandon3901NoNo
17296072METHODS AND COMPOSITIONS FOR TREATING CANCERMay 2021July 2025Allow5022NoNo
17314987TREATMENT METHOD FOR PSORIASISMay 2021February 2025Abandon4610NoNo
17290501Monoclonal Antibodies to ELTD1 and Uses ThereofApril 2021August 2025Allow5121YesNo
17287643NY-ESO-1 T CELL RECEPTORS AND METHODS OF USE THEREOFApril 2021July 2025Allow5121YesNo
17218752BISPECIFIC ANTIGEN BINDING MOLECULES WITH TRIVALENT BINDING TO CD40March 2021August 2024Abandon4001NoNo
17278509INTRABODIES FOR REDUCING FUT8 ACTIVITYMarch 2021December 2024Allow4511NoNo
17202004METHODS AND MATERIALS FOR MODULATING AN IMMUNE RESPONSEMarch 2021December 2024Abandon4511NoNo
17273538MONOCLONAL ANTIBODIES AGAINST ENDOTROPHIN AND THE USE THEREOFMarch 2021February 2025Allow4721YesNo
17186704MATERIALS AND METHODS FOR MODULATING AN IMMUNE RESPONSEFebruary 2021November 2025Allow5731YesNo
17270947ANTI-CD47 ANTIBODY AND APPLICATION THEREOFFebruary 2021March 2024Allow3600YesNo
17269315ANTAGONISTIC ANTI-TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY POLYPEPTIDESFebruary 2021January 2026Allow5921NoNo
17176427TREATMENT OF TRIPLE NEGATIVE BREAST CANCER WITH TARGETED TGF-B INHIBITIONFebruary 2021June 2024Abandon4010NoNo
17175086ANTI-INTERFERON GAMMA ANTIBODIES AND USES THEREOFFebruary 2021April 2025Allow5021YesNo
17174231ENGINEERED BISPECIFIC PROTEINSFebruary 2021August 2024Abandon4211NoNo
17266966PROTEINS BINDING NKG2D, CD16 AND A TUMOR-ASSOCIATED ANTIGENFebruary 2021January 2025Allow4720YesYes
17266092ANTI-SIGLEC ANTIBODY, PHARMACEUTICAL COMPOSITION COMPRISING THE SAME, AND USES THEREOFFebruary 2021June 2024Allow4010NoNo
17265879PROTEINS BINDING NKG2D, CD16 AND A TUMOR-ASSOCIATED ANTIGENFebruary 2021June 2025Abandon5221NoNo
17265095ANTI-ROR1 MONOCLONAL ANTIBODY, FUNCTIONAL FRAGMENT THEREOF, GENE, DRUG DELIVERY COMPOSITION, AND PHARMACEUTICAL COMPOSITIONFebruary 2021August 2024Abandon4310NoNo
17264972MUSCLE TARGETING COMPLEXES AND USES THEREOF FOR TREATING HYPERTROPHIC CARDIOMYOPATHYFebruary 2021January 2024Abandon3610NoNo
17164334MARROW INFILTRATING LYMPHOCYTES (MILs) EXPRESSING CHIMERIC ANTIGEN RECEPTORS (CAR), METHOD OF MANUFACTURING SAME, AND METHOD OF USING IN THERAPYFebruary 2021July 2024Abandon4101NoNo
17265143ANTIBODY BINDING TO HUMAN HER2 AND PREPARATION METHOD AND USE THEREOFFebruary 2021January 2025Allow4810YesNo
17262629Composition for Preventing or Treating Immune-Related DiseasesJanuary 2021September 2024Abandon4410NoNo
17261488ANTI-LYPD3 CAR T-CELL THERAPY FOR THE TREATMENT OF CANCERJanuary 2021October 2024Abandon4511NoNo
17260977CHIMERIC RECEPTORS TO STEAP1 AND METHODS OF USE THEREOFJanuary 2021October 2025Abandon5731NoNo
17259868BCMA-TARGETING CHIMERIC ANTIGEN RECEPTOR AND USES THEREOFJanuary 2021February 2025Abandon4910NoNo
17259791ANTIBODY MOLECULES THAT BIND PD-L1 AND CD137January 2021September 2024Allow4411YesNo
17259816ANTI-GPC3 SINGLE-CHAIN ANTIBODY-CONTAINING CARJanuary 2021December 2024Abandon4720NoNo
17259303METHODS FOR DETECTING AND TREATING CANCERS HAVING ADENOSINE PATHWAY ACTIVATIONJanuary 2021June 2024Allow4120NoNo
17258115ANTI-SIRPalpha ANTIBODYJanuary 2021February 2024Allow3801YesNo
17254479ZIKA NEUTRALIZING ANTIBODY COMPOSITIONS AND METHODS OF USING THE SAMEDecember 2020May 2024Abandon4110NoNo
17253501BISPECIFIC ANTIBODIESDecember 2020April 2024Abandon4001NoNo
17253487ANTI-MESOTHELIN CONSTRUCTS AND USES THEREOFDecember 2020May 2024Allow4011NoNo
17252329LIGANDS TO LIGHT OR ITS RECEPTOR LTßR FOR USE IN HAEMATOLOGIC MALIGNANCIESDecember 2020June 2025Allow5430NoNo
16973125METHODS AND COMPOSITIONS RELATING TO HIGH-THROUGHPUT MODELS FOR ANTIBODY DISCOVERY AND/OR OPTIMIZATIONDecember 2020April 2024Abandon4010NoNo
17250053CHIMERIC ANTIGEN RECEPTORNovember 2020September 2024Allow4611YesNo
17054217Eosinophil Cationic Protein (ECP) as a Tumor Marker for Malignant TumorsNovember 2020May 2024Abandon4210NoNo
16770193NEW DRUG SCREENING ASSAY USING REGULATORY MACROPHAGESJune 2020December 2024Abandon5411NoNo
16622901METHODS AND KITS FOR EVALUATING CLINICAL OUTCOMES OF AUTOIMMUNE DISEASEDecember 2019May 2025Allow6031YesNo

Appeals Overview

This analysis examines appeal outcomes and the strategic value of filing appeals for examiner SWARTWOUT, BRIANNA KENDALL.

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
0.8%
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 SWARTWOUT, BRIANNA KENDALL - Prosecution Strategy Guide

Executive Summary

Examiner SWARTWOUT, BRIANNA KENDALL works in Art Unit 1644 and has examined 58 patent applications in our dataset. With an allowance rate of 48.3%, this examiner allows applications at a lower rate than most examiners at the USPTO. Applications typically reach final disposition in approximately 45 months.

Allowance Patterns

Examiner SWARTWOUT, BRIANNA KENDALL's allowance rate of 48.3% places them in the 11% 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 SWARTWOUT, BRIANNA KENDALL receive 1.21 office actions before reaching final disposition. This places the examiner in the 15% 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 SWARTWOUT, BRIANNA KENDALL is 45 months. This places the examiner in the 12% 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 +78.9% benefit to allowance rate for applications examined by SWARTWOUT, BRIANNA KENDALL. This interview benefit is in the 99% 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, 46.4% of applications are subsequently allowed. This success rate is in the 96% 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 50.0% of cases where such amendments are filed. This entry rate is in the 74% percentile among all examiners. Strategic Recommendation: This examiner shows above-average receptiveness to after-final amendments. If your amendments clearly overcome the rejections and do not raise new issues, consider filing after-final amendments before resorting to an RCE.

Appeal Withdrawal and Reconsideration

This examiner withdraws rejections or reopens prosecution in 100.0% of appeals filed. This is in the 87% percentile among all examiners. Of these withdrawals, 100.0% occur early in the appeal process (after Notice of Appeal but before Appeal Brief). Strategic Insight: This examiner frequently reconsiders rejections during the appeal process compared to other examiners. Per MPEP § 1207.01, all appeals must go through a mandatory appeal conference. Filing a Notice of Appeal may prompt favorable reconsideration even before you file an Appeal Brief.

Petition Practice

When applicants file petitions regarding this examiner's actions, 66.7% are granted (fully or in part). This grant rate is in the 71% percentile among all examiners. Strategic Note: Petitions show above-average success regarding this examiner's actions. Petitionable matters include restriction requirements (MPEP § 1002.02(c)(2)) and various procedural issues.

Examiner Cooperation and Flexibility

Examiner's Amendments: This examiner makes examiner's amendments in 0.0% of allowed cases (in the 2% 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 7.1% of allowed cases (in the 85% 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.
  • 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.
  • Appeal filing as negotiation tool: This examiner frequently reconsiders rejections during the appeal process. Filing a Notice of Appeal may prompt favorable reconsideration during the mandatory appeal conference.
  • 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.