Prosecution Insights
Last updated: April 19, 2026
Application No. 17/707,432

Steviol Glycoside Compositions for Oral Ingestion or Use

Non-Final OA §102
Filed
Mar 29, 2022
Examiner
MORNHINWEG, JEFFREY P
Art Unit
1793
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Cargill Incorporated
OA Round
7 (Non-Final)
36%
Grant Probability
At Risk
7-8
OA Rounds
3y 11m
To Grant
70%
With Interview

Examiner Intelligence

Grants only 36% of cases
36%
Career Allow Rate
200 granted / 558 resolved
-29.2% vs TC avg
Strong +34% interview lift
Without
With
+33.7%
Interview Lift
resolved cases with interview
Typical timeline
3y 11m
Avg Prosecution
62 currently pending
Career history
620
Total Applications
across all art units

Statute-Specific Performance

§101
3.0%
-37.0% vs TC avg
§103
48.8%
+8.8% vs TC avg
§102
15.6%
-24.4% vs TC avg
§112
22.0%
-18.0% vs TC avg
Black line = Tech Center average estimate • Based on career data from 558 resolved cases

Office Action

§102
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Status of the Application Receipt of the Request for Continued Examination (RCE under 37 CFR 1.114), the Response and Amendment filed 03/16/2026 is acknowledged. The status of the claims upon entry of the present amendment stands as follows: Pending claims: 1-17, 20, and 21 Withdrawn claims: None Previously canceled claims: 18 and 19 Newly canceled claims: None Amended claims: 1, 6, 8-10, 16, 17, 20, and 21 New claims: None Claims currently under consideration: 1-17, 20, and 21 Currently rejected claims: 1-17, 20, and 21 Allowed claims: None Continued Examination Under 37 CFR 1.114 A request for continued examination under 37 CFR 1.114, including the fee set forth in 37 CFR 1.17(e), was filed in this application after final rejection. Since this application is eligible for continued examination under 37 CFR 1.114, and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114. Applicant's submission filed on 03/16/2026 has been entered. Claim Rejections - 35 USC § 102 The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior Office action. Claims 1-17, 20 and 21 are rejected under 35 U.S.C. 102(a)(2) as being anticipated by Jackson (U.S. 2017/0006906 A1). Regarding claim 1, Jackson discloses a sweetener composition ([0002], [0113]) comprising SG348 ([0117], “Rebaudioside M G2”; p. 11, column 1, figure, where Rebaudioside M G2 may comprise “-9H, -glucosyl” at R1 and “-9H, -glucosyl” at R2, with the two glucosyl moieties being at carbon atoms that causes the compound to be equivalent to that claimed in SG348, see label A in the figure below). MPEP 2131.02 II states: “when the species is clearly named, the species claim is anticipated no matter how many other species are additionally named.” The disclosure of Jackson is considered to clearly name a compound that is equivalent to SG348 due to there being 10 instances of each of the “R1” and “R2” positions, any two of which (i.e., one R1 and one R2) may individually be the position at which the two “-glucosyl” substituents are added. [AltContent: textbox (A)][AltContent: arrow][AltContent: textbox (A)][AltContent: textbox (A)][AltContent: arrow][AltContent: arrow] PNG media_image1.png 726 418 media_image1.png Greyscale [AltContent: textbox ()] As for claim 2, Jackson discloses the sweetener as further comprising rebaudioside D ([0113], [0103]). As for claim 3, Jackson discloses the sweetener as further comprising rebaudioside A ([0113], [0103]). As for claim 4, Jackson discloses the sweetener as comprising rebaudioside D in an amount in the range of 10-500 times greater than any of the supplementary steviol glycosides ([0127]-[0128]), where there may be multiple glycosylated steviol glycosides ([0113]), and where one of the glycosylated steviol glycosides may be “Rebaudioside M G1” that may comprise hydrogen at all ten R1 positions and one -glucosyl substituent at the carbon that causes the compound to be equivalent to that claimed for SG102 ([0117], p. 11, column 1, rebaudioside M figure). As for claim 5, Jackson discloses the sweetener as comprising rebaudioside D in an amount in the range of 20-200 times greater than any of the supplementary steviol glycosides ([0127]-[0128]), where there may be multiple glycosylated steviol glycosides ([0113]), and where one of the glycosylated steviol glycosides may be “Rebaudioside M G1” that may comprise hydrogen at all ten R1 positions and one -glucosyl substituent at the carbon that causes the compound to be equivalent to that claimed for SG102 ([0117], p. 11, column 1, rebaudioside M figure). As for claim 6, Jackson discloses a beverage comprising a glucosylated steviol glycoside ([0132]) that may be SG348 as was detailed previously in relation to claim 1. As for claim 7, Jackson discloses the beverage as having a total steviol glycoside amount in the range of 50-1,000 ppm ([0127]). As for claim 8, Jackson discloses the compound may be in an amount ranging from about 0 to about 2000 ppm ([0127]), which includes amounts that would be below the sweetness perception threshold. As for claim 9, Jackson discloses the compound may be in an amount ranging from about 0 to about 2000 ppm ([0127]), which includes amounts that would have a SEV of <1.0. Regarding claim 10, Jackson discloses a method of modifying a sensory characteristic of a composition, comprising adding a sensory modifying amount of a glycosylated steviol glycoside and an amount of rebaudioside A to provide a first composition, wherein the sensory modifying amount alters a sensory characteristic of the first composition relative to a second composition having the same amount of rebaudioside A without the sensory-modifying amount (specifically, “improved sweetness in comparison to each component separately”) ([0127]), where the glycosylated steviol glycoside may be SG348 as was detailed previously in relation to claim 1. As for claim 11, Jackson discloses the sensory characteristic is sweetness ([0127]). As for claim 12, Jackson discloses the sensory characteristic is “improved sweetness” ([0127]), which is considered to include an improvement in sweetness linger ([0010]). As for claim 13, Jackson discloses the sensory characteristic is “improved sweetness” ([0127]), which is considered to include an improvement in sweetness linger ([0010]), for rebaudioside M ([0127]). As for claim 14, Jackson discloses the composition as being a beverage ([0132]). As for claim 15, Jackson discloses rebaudioside D and/or rebaudioside M as being present in the beverage in an amount ranging from 0.05-1.0 g/L (specifically, about 0-2000 ppm, or 0-2.0 g/L) ([0127]). As for claim 16, Jackson discloses the compound may be in an amount ranging from 0.001-0.1 g/L (specifically, about 0-2000 ppm, or 0-2.0 g/L) ([0127]-[0128]). As for claim 17, Jackson discloses the compound, and the total glycoside concentration, may be in an amount ranging from 0.001-0.1 g/L (specifically, about 0-2000 ppm, or 0-2.0 g/L) ([0127]-[0128]). As for claim 20, Jackson discloses the sweetener composition of claim 1, comprising a sensory modifying amount of a glycosylated steviol glycoside that alters at least one sensory characteristic of the composition relative to a composition that lacks the glycosylated steviol glycoside (specifically, “improved sweetness in comparison to each component separately”) ([0127]), where the glycosylated steviol glycoside may be SG348 as was detailed previously in relation to claim 1. As for claim 21, Jackson discloses a method of altering a sensory characteristic of a composition comprising adding a sensory modifying amount of a glycosylated steviol glycoside to provide a first composition, wherein the sensory modifying amount alters at least one sensory characteristic of the composition relative to a composition that lacks the glycosylated steviol glycoside (specifically, “improved sweetness in comparison to each component separately”) ([0127]), where the glycosylated steviol glycoside may be SG348 as was detailed previously in relation to claim 1. Response to Arguments Claim Rejections - 35 U.S.C. § 102(a)(2) of claims 1-17, 20, and 21 over Jackson as evidenced by Prakash et al.: Applicant’s argument that Jackson does not disclose any of the claimed steviol glycosides (Applicant’s Remarks, p. 6, ¶6) is not persuasive. Jackson et al. discloses SG348 as detailed previously herein. The rejections of claims 1-17, 20, and 21 have been maintained herein. Conclusion Claims 1-17, 20, and 21 are rejected. No claims are allowed at this time. Any inquiry concerning this communication or earlier communications from the examiner should be directed to JEFFREY P MORNHINWEG whose telephone number is (571)270-5272. The examiner can normally be reached 8:30AM-5:00PM. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Emily Le can be reached at 571-272-0903. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /JEFFREY P MORNHINWEG/Primary Examiner, Art Unit 1793
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Prosecution Timeline

Mar 29, 2022
Application Filed
Apr 21, 2023
Non-Final Rejection — §102
Sep 25, 2023
Response Filed
Jan 05, 2024
Final Rejection — §102
Jan 19, 2024
Response after Non-Final Action
Jan 23, 2024
Response after Non-Final Action
Jan 30, 2024
Request for Continued Examination
Feb 04, 2024
Response after Non-Final Action
Aug 10, 2024
Non-Final Rejection — §102
Nov 12, 2024
Response Filed
Feb 21, 2025
Final Rejection — §102
Jun 16, 2025
Request for Continued Examination
Jun 18, 2025
Response after Non-Final Action
Jul 11, 2025
Non-Final Rejection — §102
Nov 11, 2025
Response Filed
Nov 19, 2025
Final Rejection — §102
Mar 16, 2026
Request for Continued Examination
Mar 18, 2026
Response after Non-Final Action
Mar 24, 2026
Non-Final Rejection — §102 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12599157
NATURAL SWEETENING FLAVOR COMPOSITION
2y 5m to grant Granted Apr 14, 2026
Patent 12550923
ALLULOSE SYRUPS
2y 5m to grant Granted Feb 17, 2026
Patent 12520863
Compositions used for sweetened substances
2y 5m to grant Granted Jan 13, 2026
Patent 12514274
GRANULATION OF A STEVIA SWEETENER
2y 5m to grant Granted Jan 06, 2026
Patent 12490754
WHEY PROTEIN-BASED, HIGH PROTEIN, YOGHURT-LIKE PRODUCT, INGREDIENT SUITABLE FOR ITS PRODUCTION, AND METHOD OF PRODUCTION
2y 5m to grant Granted Dec 09, 2025
Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

7-8
Expected OA Rounds
36%
Grant Probability
70%
With Interview (+33.7%)
3y 11m
Median Time to Grant
High
PTA Risk
Based on 558 resolved cases by this examiner. Grant probability derived from career allow rate.

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