IP Library Granted Patent US 11,185,367
Granted Patent B2
US 11,185,367 · App. 17/189,772 · Granted Nov 30, 2021

Methods and systems for treating diabetes and related diseases and disorders

Inventors: Harith Rajagopalan (Wellesley Hills, MA); Jay Caplan (Belmont, MA); Craig M. Gardner (Belmont, MA); J. Christopher Flaherty (Auburndale, FL)
Assignee: Fractyl Health, Inc.
A61B18/1492A61M29/02A61B2018/0022A61B2018/00029A61B2018/0041A61B2018/00196A61B2018/00404A61B2018/00577A61B2018/00779A61B2018/00797A61B2018/00839A61B2018/00875A61B2018/00994A61B2018/1467A61M2025/0087
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Quick Facts
Patent No.
US 11,185,367
App. No.
17/189,772
Granted
Nov 30, 2021
Kind
B2
Abstract

Systems, devices and methods treat target tissue to provide a therapeutic benefit to the patient. A tissue treatment device comprises a tissue treatment element constructed and arranged to treat target tissue, such as duodenal mucosa and/or submucosal tissue. Patients treated can safely eliminate or reduce their daily insulin intake.

Claims (30)

1. A method of treating a medical condition of a patient, the method comprising:

selecting a patient diagnosed with type 2 diabetes that is being treated with daily insulin at a first dosage level and having a first HbA1c level of at least 7.5%; and

performing a tissue treatment procedure comprising treating one or more segments of the selected patient's intestinal tissue, wherein the tissue segments comprise duodenal mucosal tissue and/or duodenal submucosal tissue;

wherein after the tissue treatment procedure is performed, the selected patient receives daily insulin at a second dosage level less than the first dosage level and maintains a second HbA1c level that is no greater than the first HbA1c level and wherein the method results in a therapeutic benefit to the selected patient comprising a reduced risk of hypoglycemia wherein the risk of hypoglycemia is reduced to a level of no more than 0.1% occurrence rate of serious hypoglycemic events per year.

2. The method according to claim 1 , wherein the selected patient has a c-peptide level of at least 0.5 ng/mL prior to the performing of the tissue treatment procedure.

3. The method according to claim 1 , wherein the second HbA1c level comprises an HbA1c level of the selected patient measured 24 weeks after the performance of the tissue treatment procedure.

4. The method according to claim 1 , wherein the second HbA1c level is less than the first HbA1c level.

5. The method according to claim 4 , wherein the second HbA1c level comprises a level of at least 0.5% less than the first HbA1c level.

6. The method according to claim 1 , wherein the second HbA1c level comprises an HbA1c level less than or equal to 7.5%.

7. The method according to claim 6 , wherein the second HbA1c level comprises an HbA1c level less than or equal to 7.0%.

8. The method according to claim 6 , wherein the second dosage level is zero units of insulin per day.

9. The method according to claim 1 , wherein the tissue treatment procedure comprises ablating the duodenal mucosal tissue and/or duodenal submucosal tissue.

10. The method according to claim 1 , wherein the tissue treatment procedure comprises ablating neuronal cells of the duodenal mucosa and/or duodenal submucosa.

11. The method according to claim 1 , wherein the tissue treatment procedure comprises a tissue treatment selected from the group consisting of: thermal coagulation; desiccation; non-desiccating tissue ablation; heat ablation; cryoablation; radiofrequency ablation; electroporation; ultrasound and/or other sound-based ablation; sonoporation; laser and/or other light-based ablation; mechanical abrasion; chemical abrasion and/or chemical ablation; and combinations thereof.

12. The method according to claim 1 , wherein the method results in a therapeutic benefit to the selected patient comprising a decrease in total body weight.

13. The method according to claim 1 , wherein the method results in a therapeutic benefit to the selected patient comprising a weight loss of at least 5% of the patient's weight prior to the performing of the tissue treatment procedure.

14. The method according to claim 1 , wherein the second dosage level is zero units of insulin per day.

15. The method according to claim 1 , wherein the second dosage level is no more than 50% of the first dosage level.

16. The method according to claim 1 , wherein the first dosage level comprises a level of at least 10 units of insulin per day.

17. The method according to claim 16 , wherein the first dosage level comprises a level of at least 20 units of insulin per day.

18. The method according to claim 16 , wherein the first dosage level comprises a level of at least 50 units of insulin per day.

19. The method according to claim 16 , wherein the first dosage level comprises a level of at least 60 units of insulin per day.

20. The method according to claim 1 , wherein the first dosage level comprises a level of at least 0.5 units of insulin per kilogram of patient body weight per day.

21. The method according to claim 1 , wherein at the time of selection, the selected patient is further taking a non-insulin anti-diabetic medication.

22. The method according to claim 1 , wherein at the time of selection, the selected patient has a c-peptide level of at least 0.6 ng/mL.

23. The method according to claim 22 , wherein at the time of selection, the selected patient has a c-peptide level of at least 1.0 ng/mL.

24. The method according to claim 1 , wherein at the time of selection, the selected patient further comprises a patient with a fasting plasma glucose level of at least 140 mg/dL.

25. The method according to claim 24 , wherein at the time of selection, the selected patient further comprises a patient with a fasting plasma glucose level of at least 160 mg/dL.

26. The method according to claim 24 , wherein at the time of selection, the selected patient further comprises a patient with a fasting plasma glucose level of at least 180 mg/dL.

27. The method according to claim 1 , wherein the method further comprises the selected patient taking at least one non-insulin anti-diabetic medication after the performance of the tissue treatment procedure.

Assignments (3)
SECURITY INTEREST Recorded Sep 7, 2023
From: FRACTYL HEALTH, INC.
To: SYMBIOTIC CAPITAL AGENCY LLC
Reel/Frame 064840/0561 →
CHANGE OF NAME Recorded Oct 4, 2021
From: FRACTYL LABORATORIES, INC.
To: FRACTYL HEALTH, INC.
Reel/Frame 057710/0228 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2021
From: RAJAGOPALAN, HARITH; CAPLAN, JAY; GARDNER, CRAIG M.; FLAHERTY, J. CHRISTOPHER
To: FRACTYL LABORATORIES, INC.
Reel/Frame 056979/0334 →
Continuity (8)
Continuation 17096855 · Nov 12, 2020
Continuation 15406572 · Jan 13, 2017
Continuation PCTUS2015040775 · Jul 16, 2015
Provisional Application 63085375 · Sep 30, 2020
Provisional Application 63076737 · Sep 10, 2020
Provisional Application 62991219 · Mar 18, 2020
Provisional Application 62025307 · Jul 16, 2014
Related Publication 20210220045A1 · Jul 22, 2021
Cited By (6)
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