IP Library Granted Patent US 11,559,618
Granted Patent B2
US 11,559,618 · App. 17/661,737 · Granted Jan 24, 2023

Formulations and methods for direct sodium removal in patients having severe renal dysfunction

Inventors: Jeffrey Testani (Guilford, CT); Christopher McIntyre (Ontario, CA); Ian Crosbie (London, GB); Oliver Goedje (Strasslach, DE)
Assignee: Sequana Medical NV
A61M1/282A61K9/0019A61K9/08A61K31/7004A61K31/716A61K33/14A61M1/28A61M1/285A61M1/287A61M27/002A61M31/002A61P7/08A61L2/0047A61L2202/21A61M2205/18A61M2205/3317A61M2205/3337A61M2205/3344A61M2205/3368A61M2205/3379A61M2205/3569A61M2205/3576A61M2205/502A61M2205/52A61M2205/587A61M2205/6009A61M2205/70A61M2205/8206A61M2205/8243A61M2209/086A61M2209/088A61M2210/1017A61M2210/1085
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Quick Facts
Patent No.
US 11,559,618
App. No.
17/661,737
Granted
Jan 24, 2023
Kind
B2
Abstract

A direct sodium removal (“DSR”) infusate regimen and methods of use are provided for removing sodium and reducing fluid overload in patients with severe renal dysfunction and/or heart failure, in which a patient has at least a first DSR session with a first DSR infusate having no or low sodium that is instilled into a patient's peritoneal cavity for a first dwell period to cause sodium and excess fluid to migrate to the patient's peritoneal cavity, and thereafter, the patient may undergo conventional dialysis to rebalance the patient's fluid and sodium levels.

Claims (26)

1. An infusate regimen for use in removing excess sodium and fluid from a patient having fluid overload or severe renal dysfunction, the infusate regimen comprising:

a first direct sodium removal (“DSR”) infusate formulated to be administered by infusion into, and removal from, a peritoneal cavity of a patient, the first DSR infusate having a first osmolality in which an aqueous solution contains a sodium concentration equal to or less than 35 meq/L and at least one of zero to 50 grams of dextrose per 100 ml of aqueous solution, 0.5 to 50 grams of icodextrin per 100 ml of aqueous solution, 0.5 to 50 grams of a high molecular weight biocompatible polymer having an average molecular weight greater than 10,000 Daltons per 100 ml of aqueous solution, or solutions containing any one or more of 0.5 to 50 grams of xylitol, glycerol, hyperbranched polyglycerol, sorbitol, carnitine, taurine, amino acids, urea, polyacrylate, polyethyleneimine, or stevioside per 100 ml of aqueous solution, or any combination thereof.

2. The infusate regimen of claim 1 , further comprising:

a second DSR infusate formulated to be administered by infusion into, and removal from, the peritoneal cavity of the patient, the second DSR infusate having a second osmolality in which an aqueous solution contains a sodium concentration equal to or less than 35 meq/L and at least one of zero to 50 grams of dextrose per 100 ml of aqueous solution, 0.5 to 50 grams of icodextrin per 100 ml of aqueous solution, or 0.5 to 50 grams of a high molecular weight biocompatible polymer having an average molecular weight greater than 10,000 Daltons per 100 ml of aqueous solution, or solutions containing any one or more of 0.5 to 50 grams of xylitol, glycerol, hyperbranched polyglycerol, sorbitol, carnitine, taurine, amino acids, urea, polyacrylate, polyethyleneimine or stevioside per 100 ml of aqueous solution, or any combination thereof, wherein the second osmolality is different than the first osmolality.

3. The infusate regimen of claim 1 , wherein the first DSR infusate has an osmolality and sodium concentration selected to induce a steep sodium gradient between a patient's blood serum sodium level and the first DSR infusate when instilled into the peritoneal cavity during a first dwell period.

4. The infusate regimen of claim 2 , wherein the second DSR infusate has an osmolality and sodium concentration selected to induce a shallow sodium gradient between the patient's blood serum sodium level and the second DSR infusate when instilled into the peritoneal cavity during a second dwell period.

5. The infusate regimen of claim 1 , wherein the first DSR infusate is sodium-free.

6. The infusate regimen of claim 2 , wherein the first DSR infusate or second DSR infusate further comprises an electrolyte selected from among a magnesium salt and a calcium salt.

7. The infusate regimen of claim 2 , wherein the first DSR infusate or second DSR infusate further comprises at least one of: an antimicrobial agent, an antifungal agent, and a buffering agent.

8. The infusate regimen of claim 1 , wherein the first DSR infusate is formulated to be sufficiently nonviscous that the infusate may be instilled into the peritoneal cavity from a reservoir via gravity feed.

9. The infusate regimen of claim 2 , wherein the second DSR infusate is formulated to be sufficiently nonviscous that the infusate may be instilled into the peritoneal cavity from a reservoir via gravity feed.

10. The infusate regimen of claim 2 , wherein the each of the first DSR infusate and the second DSR infusate are formulated to be instilled into a patient's peritoneal cavity in an amount between 0.25 liter and 2.0 liter per DSR session.

11. A method of reducing fluid overload in a patient suffering from severe renal dysfunction or heart failure, the method comprising:

administering a first DSR infusate having no or low sodium and a first osmolality into a peritoneal cavity of a patient to induce sodium and osmotic ultrafiltrate to accumulate with the first DSR infusate in the peritoneal cavity during a first dwell period, wherein the first DSR infusate has a first osmolality in which an aqueous solution contains a sodium concentration equal to or less than 35 meq/L and at least one of zero to 50 grams of dextrose per 100 ml of aqueous solution, 0.5 to 50 grams of icodextrin per 100 ml of aqueous solution, 0.5 to 50 grams of a high molecular weight biocompatible polymer having an average molecular weight greater than 10,000 Daltons per 100 ml of aqueous solution, or solutions containing any one or more of 0.5 to 50 grams of xylitol, glycerol, hyperbranched polyglycerol, sorbitol, carnitine, taurine, amino acids, urea, polyacrylate, polyethyleneimine, or stevioside per 100 ml of aqueous solution, or any combination thereof; and

removing the first DSR infusate, sodium and osmotic ultrafiltrate from the peritoneal cavity of the patient by pumping fluid with an implantable pump from the peritoneal cavity to a bladder of the patient, for subsequent elimination by urination.

12. The method of claim 11 , further comprising:

administering a second DSR infusate having no or low sodium and a second osmolality, different than the first osmolality, into the peritoneal cavity of the patient to induce sodium and osmotic ultrafiltrate to accumulate with the second DSR infusate in the peritoneal cavity during a second dwell period, wherein the second DSR infusate has a second osmolality in which an aqueous solution contains a sodium concentration equal to or less than 35 meq/L and at least one of zero to 50 grams of dextrose per 100 ml of aqueous solution, 0.5 to 50 grams of icodextrin per 100 ml of aqueous solution, or 0.5 to 50 grams of a high molecular weight biocompatible polymer having an average molecular weight greater than 10,000 Daltons per 100 ml of aqueous solution, or solutions containing any one or more of 0.5 to 50 grams of xylitol, glycerol, hyperbranched polyglycerol, sorbitol, carnitine, taurine, amino acids, urea, polyacrylate, polyethyleneimine or stevioside per 100 ml of aqueous solution, or any combination thereof; and

removing the second DSR infusate, sodium and osmotic ultrafiltrate from the peritoneal cavity of the patient to the bladder.

13. The method of claim 12 , wherein removing the second DSR infusate, sodium and osmotic ultrafiltrate from the peritoneal cavity of the patient comprises pumping fluid from the peritoneal cavity to a bladder of the patient with an implantable pump.

14. The method of claim 12 , further comprising, between administering a first DSR infusate and administering a second DSR infusate or thereafter, adjusting a serum sodium level of the patient by conducting hemodialysis or peritoneal dialysis.

15. The method of claim 12 , wherein administering a first DSR infusate or a second DSR infusate comprises introducing a DSR infusate containing dextrose or Icodextrin or combinations thereof.

16. The method of claim 12 , wherein administering a first DSR infusate or a second DSR infusate comprises introducing a DSR infusate via a subcutaneous port or a conventional peritoneal dialysis catheter.

17. The method of claim 11 , further comprising monitoring a serum sodium level of the patient during the first dwell period.

18. The method of claim 11 , wherein the first DSR infusate has an osmolality and sodium concentration selected create a steep sodium gradient between a patient's blood serum sodium level and the first DSR infusate when instilled into the peritoneal cavity during the first dwell period.

19. The method of claim 12 , wherein the second DSR infusate has an osmolality and sodium concentration selected to create a shallow sodium gradient between a person's blood serum sodium level and the second DSR infusate when instilled into the peritoneal cavity during the second dwell period.

20. The method of claim 12 , wherein administering each of the first DSR infusate and the second DSR infusate comprises instilling into the patient's peritoneal cavity an amount between 0.25 liter and 2.0 liter of fluid per DSR session.

Assignments (4)
SECURITY INTEREST Recorded Feb 27, 2025
From: DSRCO BV
To: KREOS CAPITAL VII (UK) LIMITED
Reel/Frame 070356/0934 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2025
From: SEQUANA MEDICAL NV
To: DSRCO BV
Reel/Frame 070308/0171 →
SECURITY INTEREST Recorded Sep 25, 2024
From: SEQUANA MEDICAL NV
To: KREOS CAPITAL VII (UK) LIMITED
Reel/Frame 069049/0129 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2022
From: TESTANI, JEFFREY; MCINTYRE, CHRISTOPHER; CROSBIE, IAN; GOEDJE, OLIVER
To: SEQUANA MEDICAL NV
Reel/Frame 060263/0215 →
Continuity (4)
Continuation In Part 17174855 · Feb 12, 2021
Continuation 15985598 · May 21, 2018
Provisional Application 62510652 · May 24, 2017
Related Publication 20220257843A1 · Aug 18, 2022
Cited By (2)
US 12,496,384 US 12,623,011