USPTO Examiner SOROUSH LAYLA - Art Unit 1622

Recent Applications

Detailed information about the 100 most recent patent applications.

Application NumberTitleFiling DateDisposal DateDispositionTime (months)Office ActionsRestrictionsInterviewAppeal
19274086TOPICAL FORMULATION FOR A JAK INHIBITORJuly 2025January 2026Allow600YesNo
19212445COMPOSITIONS AND METHODS FOR TREATMENT OF PERI-IMPLANTITIS AND PERIODONTITISMay 2025August 2025Allow300YesNo
19171214TOPICAL FORMULATION FOR JAK INHIBITORApril 2025October 2025Allow601YesNo
19060423FAST ABSORBING TROLAMINE SALICYLATE FORMULATIONS AND COMPOSITIONSFebruary 2025October 2025Allow701YesNo
19016312READY-TO-USE NON-AQUEOUS ORAL SOLUTION OF LOSARTANJanuary 2025August 2025Allow710YesNo
18974530Preparation Method and Application of Micelle Preparation Containing Thymol and Derivative ThereofDecember 2024March 2025Allow300YesNo
18941896Progestin/Testosterone Transdermal GelNovember 2024August 2025Allow921YesNo
18934749STABLE LEVOTHYROXINE COMPOSITIONS IN APROTIC POLAR SOLVENTSNovember 2024November 2025Allow1320YesNo
18884931METHODS OF REDUCING ITCH USING TOPICAL ROFLUMILAST COMPOSITIONSSeptember 2024August 2025Abandon1110YesNo
18814130PHARMACEUTICAL RECTAL SUPPOSITORY COMPOSITIONS OF 6-THIOGUANINE, METHODS OF TREATMENT AND/OR METHODS OF MANUFACTURINGAugust 2024January 2026Allow1721YesNo
18794128AMLODIPINE FORMULATIONSAugust 2024April 2025Allow811NoNo
18768656TOPICAL OPHTHALMOLOGICAL COMPOSITIONSJuly 2024August 2025Allow1310YesNo
18659957TOPICAL COMPOSITIONS AND METHODS FOR TREATING INFLAMMATORY SKIN DISEASESMay 2024December 2025Abandon1901NoNo
18638564SYSTEMS AND METHODS FOR DELIVERY OF PHENYLALANINE AND LACTATEApril 2024October 2025Abandon1810NoNo
18600419NON-SEDATING DEXMEDETOMIDINE TREATMENT REGIMENSMarch 2024April 2025Allow1310NoNo
18600431NON-SEDATING DEXMEDETOMIDINE TREATMENT REGIMENSMarch 2024August 2024Allow610NoNo
18590910ANALGESIC AND ANTIPRURITIC PHARMACERTICAL COMPOSITION AND APPLICATION THEREOFFebruary 2024February 2025Allow1100YesNo
18588626TOPICAL FORMULATION FOR A JAK INHIBITORFebruary 2024December 2024Allow1010YesNo
18441397STABLE PHARMACEUTICAL COMPOSITIONS OF CYCLOPHOSPHAMIDEFebruary 2024January 2025Abandon1110NoNo
18528684STABLE PHARMACEUTICAL COMPOSITIONS OF SUCCINYLCHOLINE CHLORIDEDecember 2023August 2024Allow920YesNo
18526030METHOD FOR IMPROVING THE SENSORIAL PROPERTIES OF OIL-IN-WATER EMULSIONS, TO REDUCE THE ADHESIVE EFFECT OF SUCH GLYCERIN-BASED OIL-IN-WATER EMULSIONSDecember 2023February 2025Allow1410YesNo
18515184PROCESS FOR OBTAINING A PURIFIED PSYCHOACTIVE ALKALOID SOLUTIONNovember 2023February 2026Abandon2731NoNo
18487671SUSTAINED RELEASE AMINOPYRIDINE COMPOSITIONOctober 2023April 2025Abandon1811NoNo
18374860COMPOSITIONS AND METHODS FOR THE TREATMENT OF ADDICTION AND OTHER NEUROPSYCHIATRIC DISORDERSSeptember 2023October 2025Abandon2401NoNo
18478029AR+BREAST CANCER TREATMENT METHODSSeptember 2023February 2025Allow1610YesNo
18455759USE OF LEVODOPA, CARBIDOPA AND ENTACAPONE FOR TREATING PARKINSON'S DISEASEAugust 2023September 2025Allow2520YesNo
18455242TOPICAL DETOMIDINE FORMULATIONSAugust 2023March 2025Abandon1910NoNo
18221164PHARMACEUTICAL FORMULATION FOR THE TREATMENT OF INFLAMMATORY CHANGES TO THE RECTUMJuly 2023August 2025Allow2620YesYes
18345692Method and Formulation for Improving Roflumilast Skin Penetration Lag TimeJune 2023August 2025Abandon2630YesNo
18345732Method and Formulation for Improving Roflumilast Skin Penetration Lag TimeJune 2023August 2025Abandon2640YesNo
18339206METHOD FOR TREATING INFECTIONSJune 2023December 2025Abandon3011NoNo
18334084USE OF TOPICAL BRAF INHIBITOR COMPOSITIONS FOR TREATMENT OF EPIDERMAL GROWTH FACTOR RECEPTOR DOWNSTREAM EFFECTORS - INDUCED CUTANEOUS REACTIONSJune 2023May 2025Abandon2431NoNo
18123828TOPICAL COMPOSITIONMarch 2023September 2025Allow3020YesNo
18024943ANTICOCCIDIAL COMPOSITION COMPRISING COUMARIC ACID AND USE THEREOFMarch 2023February 2026Allow3510YesNo
18176296NON-SEDATING DEXMEDETOMIDINE TREATMENT REGIMENSFebruary 2023February 2026Abandon3540NoYes
18174706DIETARY PRODUCT DEVOID OF AT LEAST TWO NON ESSENTIAL AMINO ACIDSFebruary 2023September 2025Allow3150YesNo
18022886Nano-Emulsion Based Compositions, Methods for Their Preparation and Their Use in Delivery of Active IngredientsFebruary 2023January 2025Allow2321YesNo
18096165COMBINATION OF AN ANTIALLERGIC AGENT WITH MUSCARINIC ANTAGONIST AND/OR DOPAMINERGIC AGONIST FOR USE IN PREVENTING/STOPPING OF AXIAL MYOPIA IN HUMANJanuary 2023October 2025Abandon3330NoNo
18077296COMPOSITIONS OF BILE ACIDS AND PHENYLBUTYRATE COMPOUNDSDecember 2022December 2024Allow2410NoNo
17925382SOLID LIPID NANO-COMPOSITION CONTAINING BERBERINE AND CINNAMONALDEHYDE EFFECTIVE IN TREATING DIABETES, DYSLIPIDEMIA, AND METHOD OF PREPARING THE SAMENovember 2022January 2026Allow3810YesNo
17921865LIQUID FORMULATION AND PHARMACEUTICAL PRODUCT CONTAINING CILASTATINOctober 2022March 2026Abandon4101NoNo
17959069SYSTEMS AND METHODS FOR DELIVERY OF N-LACTOYL-PHENYLALANINE AND OTHER N-LACTOYL-AMINO ACIDSOctober 2022August 2025Abandon3461NoNo
17942505PHARMACEUTICAL COMPOSITION CONTAINING B-LAPACHONE AS ACTIVE INGREDIENT FOR PREVENTION OR TREATMENT OF CHOLESTATIC LIVER DISEASESeptember 2022May 2024Allow2030YesNo
17820783METHODS OF ADMINISTERING INTRAVENOUS MELOXICAM IN A BOLUS DOSEAugust 2022April 2025Abandon3210NoNo
17887798SELF-PRESERVING TOPICAL PHARMACEUTICAL COMPOSITIONS COMPRISING DIETHYLENE GLYCOL MONOETHYL ETHERAugust 2022January 2026Abandon4130YesNo
17887826Dosing Regimens Associated With Extended Release Paliperidone Injectable FormulationsAugust 2022July 2025Allow3520YesNo
17877602USE OF NICOLSAMIDE FORMULATIONS FOR ANTIVIRAL THERAPYJuly 2022March 2026Abandon4301NoNo
17758783COMPOSITIONS COMPRISING DESOXIMETASONE AND TAZAROTENEJuly 2022December 2025Abandon4101NoNo
17789907APREPITANT FOR USE IN THE TOPICAL TREATMENT OF FACIAL NEURALGIAJune 2022December 2025Abandon4110NoNo
17847205TOPICAL PHARMACEUTICAL FORMULATIONJune 2022September 2025Allow3930YesNo
17787187TOPICAL PHARMACEUTICAL COMPOSITIONS FOR TREATING ONYCHOMYCOSISJune 2022January 2026Abandon4301NoNo
17840502VAPORIZABLE PSYCHOACTIVE ALKALOID COMPOSITION AND PREPARATION THEREOFJune 2022November 2024Abandon2941NoNo
17782996ORALLY DISSOLVING FORMULATIONS OF PRUCALOPRIDEJune 2022February 2026Abandon4511NoNo
17804342TOPICAL TREATMENT FOR ANORECTAL DISORDERS WITH AND WITHOUT SEAT CUSHIONMay 2022June 2025Abandon3741YesNo
17738422Dosing Regimens Associated With Extended Release Paliperidone Injectable FormulationsMay 2022September 2023Allow1610YesNo
17773091IMPROVING RENAL FUNCTION AFTER KIDNEY TRANSPLANTATIONApril 2022November 2025Abandon4201NoNo
17771122TREATMENT OF INFLAMMATORY CONDITION IN MUCOUS MEMBRANE OR SKINApril 2022October 2025Allow4201YesNo
17724262PHARMACEUTICAL COMPOSITION CONTAINING B-LAPACHONE AS ACTIVE INGREDIENT FOR PREVENTION OR TREATMENT OF CHOLESTATIC LIVER DISEASEApril 2022November 2025Abandon4211NoNo
17770276METHODS FOR TREATING NEUROLOGICAL DISORDERS WITH ALPHA1A-AR PARTIAL AGONISTSApril 2022February 2026Abandon4601NoNo
17713082TOPICAL PHARMACEUTICAL COMPOSITION BASED ON SEMIFLUORINATED ALKANESApril 2022March 2025Abandon3531NoNo
17703543TREATMENT OF SKIN CONDITIONS USING HIGH KRAFFT TEMPERATURE ANIONIC SURFACTANTSMarch 2022July 2023Allow1661YesNo
176421361,4-DIHYDROBENZO[D]PYRAZOLO[3,4-F][1,3]DIAZEPINE DERIVATIVES AND RELATED COMPOUNDS AS LRRK2, NUAK1 AND/OR TYK2 KINASE MODULATORS FOR THE TREATMENT OF E.G. AUTOIMMUNE DISEASEMarch 2022April 2025Allow3700YesNo
17636917FORMULATIONS FOR USE IN THE PREVENTION AND/OR TREATMENT OF PERIPHERAL NEUROPATHY AND ITS ASSOCIATED DISEASESFebruary 2022October 2025Abandon4420NoNo
17673518USING FATTY ACID SYNTHASE INHIBITORS TO TREAT FIBROSISFebruary 2022November 2024Allow3321YesYes
17591223METHODS AND COMPOSITIONS TO PREVENT AND TREAT DISORDERS ASSOCIATED WITH MUTATIONS IN THE ODC1 GENEFebruary 2022August 2024Allow3021YesNo
17630775PROCESS FOR THE PREPARATION OF TOPICAL FORMULATIONJanuary 2022January 2026Allow4811YesNo
17629424TOPICAL JAK INHIBITOR COMBINATION COMPOSITIONS FOR TREATMENT OF INFLAMMATORY SKIN CONDITIONSJanuary 2022November 2025Abandon4601NoNo
17627692HISTONE DEACETYLASE 6 INHIBITORS AND METHOD FOR TREATING NEUROPATHIC PAINJanuary 2022January 2026Abandon4811NoNo
17624188IBUPROFEN ESTER DERIVATIVE AND EMULSION PREPARATION THEREOFDecember 2021January 2026Allow4911YesNo
17621330CBD COMPOSITIONDecember 2021October 2025Abandon4601NoNo
17554316TOPICAL ACYCLOVIR FORMULATIONS AND USES THEREOFDecember 2021March 2025Abandon3921NoNo
17541439TOPICAL FORMULATION FOR A JAK INHIBITORDecember 2021January 2026Allow4921NoNo
17614647PYRIMIDINE DERIVATIVE INHIBITING GROWTH OF CANCER CELL AND MEDICINAL USE THEREOFNovember 2021September 2025Allow4611YesNo
17496460METHODS OF MODULATING TETRABENAZINE METABOLITES PLASMA LEVELS USING BUPROPIONOctober 2021May 2025Abandon4350YesYes
17449785METHODS FOR ENHANCING THE BIOAVAILABILITY AND EXPOSURE OF A VOLTAGE-GATED POTASSIUM CHANNEL OPENEROctober 2021March 2025Abandon4121NoNo
17440778TREATMENT OF ROSACEA WITH TOPICAL COMBINATION COMPOSITIONSSeptember 2021July 2025Abandon4601NoNo
17293903BIASED NMDA RECEPTOR MODULATORS AND USES THEREOFMay 2021July 2025Allow5121YesNo
17292027NITROGEN-CONTAINING FUSED HETEROCYCLIC SHP2 INHIBITOR COMPOUND, PREPARATION METHOD, AND USEMay 2021January 2025Allow4421YesNo
17271261ACRYLATE-FREE COSMETIC EMULSIONFebruary 2021September 2025Allow5521YesNo
17165652METHODS OF TREATING EPITHELIOID CELL TUMORSFebruary 2021September 2024Allow4311NoNo
17153611TOPICAL DETOMIDINE FORMULATIONSJanuary 2021April 2025Abandon5151YesNo
17052775CANCER TREATMENTS TARGETING CANCER STEM CELLSNovember 2020September 2024Allow4740YesNo
17087365METHODS OF INDUCING ANESTHESIANovember 2020March 2025Abandon5321YesYes
16971472IMIDAZOPYRIMIDINES AS EED INHIBITORS AND THE USE THEREOFAugust 2020June 2024Allow4611YesNo
16932352TREATMENT AND MANAGEMENT OF AUGMENTATION IN RESTLESS LEGS SYNDROMEJuly 2020September 2024Allow5041YesNo
16766019RHEOLOGY ADDITIVES BASED ON DI-OR TRI-AMIDES AND MIXTURES THEREOFMay 2020February 2024Allow4551YesNo
16809662PHARMACEUTICAL FORMULATIONS COMPRISING NITROCATECHOL DERIVATIVES AND METHODS OF MAKING THEREOFMarch 2020November 2024Abandon5641YesNo
16470350METHOD FOR IMPROVING THE SENSORIAL PROPERTIES OF OIL-IN-WATER EMULSIONS, TO REDUCE THE ADHESIVE EFFECT OF SUCH GLYCERIN-BASED OIL-IN-WATER EMULSIONSJune 2019February 2025Allow6061YesNo
16365364USE OF TIOTROPIUM BROMIDE TO PREVENT PULMONARY OXYGEN TOXICITYMarch 2019February 2025Abandon6041NoYes
16246320COMBINATION OF A SELECTIVE HISTONE DEACETYLASE 3 (HDAC3) INHIBITOR AND AN IMMUNOTHERAPY AGENT FOR THE TREATMENT OF CANCERJanuary 2019June 2024Allow6051YesNo
15757266METHODS FOR TREATMENT OF MONOCYTE DYSFUNCTION AND CHRONIC INFLAMMATORY MICRO AND MACRO-VASCULAR DISEASESMarch 2018March 2026Abandon60101YesNo
15528882TREATMENT OF SKIN ATROPHY WITH A COMBINATION OF TRIIODOTHYROACETIC ACID (TRIAC) AND DEHYDROEPIANDROSTERONE (DHEA)May 2017December 2018Allow1911YesNo
15229116Therapeutic Calcium Phosphate Particles in Use for Aesthetic or Cosmetic Medicine, and Methods of Manufacture and UseAugust 2016February 2020Allow4231YesNo
15226415Formulations that Provide Support During Vaccinations and Adaptive Immune System ResponseAugust 2016December 2018Allow2821YesNo
15220617(HETERO)ARYL IMIDAZOLES/PYRAZOLES FOR TREATMENT OF NEUROLOGICAL DISORDERSJuly 2016April 2019Allow3321YesYes
14971230AQUEOUS GEL FORMULATIONS CONTAINING IMMUNE RESPONSE MODIFIERSDecember 2015April 2018Allow2821NoNo
14704375PHARMACEUTICAL COMPOSITIONS COMPRISING NEBIVOLOL OR A NEBIVOLOL ANALOGUEMay 2015June 2018Allow3841YesNo
14612143TREATING INFLAMMATION AND INFLAMMATORY PAIN IN MUCOSA USING MUCOSAL PROLONGED RELEASE BIOADHESIVE THERAPEUTIC CARRIERSFebruary 2015August 2015Allow711YesNo
14499457COMPOSITIONS AND METHODS FOR ENHANCING BRAIN FUNCTIONSeptember 2014February 2016Allow1700YesNo
14453861COMPOSITIONS AND METHODS FOR ENHANCING BRAIN FUNCTIONAugust 2014February 2016Allow1801YesNo

Appeals Overview

This analysis examines appeal outcomes and the strategic value of filing appeals for examiner SOROUSH, LAYLA.

Patent Trial and Appeal Board (PTAB) Decisions

Total PTAB Decisions
8
Examiner Affirmed
3
(37.5%)
Examiner Reversed
5
(62.5%)
Reversal Percentile
84.5%
Higher than average

What This Means

With a 62.5% reversal rate, the PTAB has reversed the examiner's rejections more often than affirming them. This reversal rate is in the top 25% across the USPTO, indicating that appeals are more successful here than in most other areas.

Strategic Value of Filing an Appeal

Total Appeal Filings
34
Allowed After Appeal Filing
18
(52.9%)
Not Allowed After Appeal Filing
16
(47.1%)
Filing Benefit Percentile
85.1%
Higher 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, 52.9% of applications that filed an appeal were subsequently allowed. This appeal filing benefit rate is in the top 25% across the USPTO, indicating that filing appeals is particularly effective here. The act of filing often prompts favorable reconsideration during the mandatory appeal conference.

Strategic Recommendations

Appeals to PTAB show good success rates. If you have a strong case on the merits, consider fully prosecuting the appeal to a Board decision.

Filing a Notice of Appeal is strategically valuable. The act of filing often prompts favorable reconsideration during the mandatory appeal conference.

Examiner SOROUSH, LAYLA - Prosecution Strategy Guide

Executive Summary

Examiner SOROUSH, LAYLA works in Art Unit 1622 and has examined 107 patent applications in our dataset. With an allowance rate of 90.7%, this examiner has an above-average tendency to allow applications. Applications typically reach final disposition in approximately 43 months.

Allowance Patterns

Examiner SOROUSH, LAYLA's allowance rate of 90.7% places them in the 74% percentile among all USPTO examiners. This examiner has an above-average tendency to allow applications.

Office Action Patterns

On average, applications examined by SOROUSH, LAYLA receive 2.79 office actions before reaching final disposition. This places the examiner in the 81% percentile for office actions issued. This examiner issues more office actions than most examiners, which may indicate thorough examination or difficulty in reaching agreement with applicants.

Prosecution Timeline

The median time to disposition (half-life) for applications examined by SOROUSH, LAYLA is 43 months. This places the examiner in the 15% 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 +4.6% benefit to allowance rate for applications examined by SOROUSH, LAYLA. This interview benefit is in the 29% percentile among all examiners. Recommendation: Interviews provide a below-average benefit with this examiner.

Request for Continued Examination (RCE) Effectiveness

When applicants file an RCE with this examiner, 17.0% of applications are subsequently allowed. This success rate is in the 15% percentile among all examiners. Strategic Insight: RCEs show lower effectiveness with this examiner compared to others. Consider whether a continuation application might be more strategic, especially if you need to add new matter or significantly broaden claims.

After-Final Amendment Practice

This examiner enters after-final amendments leading to allowance in 58.1% of cases where such amendments are filed. This entry rate is in the 84% 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.

Pre-Appeal Conference Effectiveness

When applicants request a pre-appeal conference (PAC) with this examiner, 100.0% result in withdrawal of the rejection or reopening of prosecution. This success rate is in the 69% percentile among all examiners. Strategic Recommendation: Pre-appeal conferences show above-average effectiveness with this examiner. If you have strong arguments, a PAC request may result in favorable reconsideration.

Appeal Withdrawal and Reconsideration

This examiner withdraws rejections or reopens prosecution in 76.5% of appeals filed. This is in the 68% percentile among all examiners. Of these withdrawals, 50.0% occur early in the appeal process (after Notice of Appeal but before Appeal Brief). Strategic Insight: This examiner shows above-average willingness to reconsider rejections during appeals. The mandatory appeal conference (MPEP § 1207.01) provides an opportunity for reconsideration.

Petition Practice

When applicants file petitions regarding this examiner's actions, 68.2% are granted (fully or in part). This grant rate is in the 76% 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 14.0% of allowed cases (in the 96% percentile). Per MPEP § 1302.04, examiner's amendments are used to place applications in condition for allowance when only minor changes are needed. This examiner frequently uses this tool compared to other examiners, indicating a cooperative approach to getting applications allowed. Strategic Insight: If you are close to allowance but minor claim amendments are needed, this examiner may be willing to make an examiner's amendment rather than requiring another round of prosecution.

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:

  • Expect multiple rounds of prosecution: This examiner issues more office actions than average. Address potential issues proactively in your initial response and consider requesting an interview early in prosecution.
  • 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.
  • Examiner cooperation: This examiner frequently makes examiner's amendments to place applications in condition for allowance. If you are close to allowance, the examiner may help finalize the claims.

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.