IP Library Patent Application 17516503
Patent Application
App. No. 17/516,503

METHODS AND SYSTEMS FOR TREATING DIABETES AND RELATED DISEASES AND DISORDERS

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Patent No.
US None
App. No.
17/516,503
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 (36)

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%;

advancing a treatment element of an elongate device into the duodenum of a patient;

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

removing the treatment element from the patient;

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.

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

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

4 . The method according to claim 1 , wherein the first dosage level comprises a level of at least 10 units of insulin per day, and wherein the second dosage level is no more than 50% of the first.

5 . The method according to claim 1 , wherein the first dosage level comprises a level of at least 20 units of insulin per day, and wherein the second dosage level is no more than 50% of the first.

6 . The method according to claim 1 , wherein the first dosage level comprises a level of at least 50 units of insulin per day, and wherein the second dosage level is no more than 50% of the first.

7 . The method according to claim 1 , wherein the first dosage level comprises a level of at least 60 units of insulin per day, and wherein the second dosage level is no more than 50% of the first.

8 . The method according to claim 1 , wherein the risk of hypoglycemia is reduced to a level of no more than 0.5% occurrence rate of serious hypoglycemic events per year.

9 . The method according to claim 1 , wherein the method is performed without surgery.

10 . The method according to claim 1 , wherein the method does not include implanting a chronic implant in the patient.

11 . 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.

12 . 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.

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

14 . The method according to claim 13 , wherein the second HbA1c level comprises a level of at least 0.5% less than the first HbA1c level.

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

16 . The method according to claim 15 , wherein the second HbA1c level comprises an HbA1c level less than or equal to 7.0%

17 . The method according to claim 15 , wherein the second dosage level is zero units of insulin per day.

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

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

20 . 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.

21 . 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.

22 . 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.

23 . The method according to claim 1 , wherein the method results in a therapeutic benefit to the selected patient comprising a reduced risk of hypoglycemia.

24 . 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.

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

26 . 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.

27 . The method according to claim 26 , wherein at the time of selection, the selected patient has a c-peptide level of at least 1.0 ng/mL.

28 . 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.

29 . The method according to claim 28 , 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.

30 . The method according to claim 28 , 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.

31 . 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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2021
From: RAJAGOPALAN, HARITH; CAPLAN, JAY; GARDNER, CRAIG M.; FLAHERTY, J. CHRISTOPHER
To: FRACTYL LABORATORIES, INC.
Reel/Frame 057986/0663 →
CHANGE OF NAME Recorded Nov 1, 2021
From: FRACTYL LABORATORIES, INC.
To: FRACTYL HEALTH, INC.
Reel/Frame 057988/0845 →