IP Library Granted Patent US 10,406,335
Granted Patent B2
US 10,406,335 · App. 15/473,437 · Granted Sep 10, 2019

Drug delivery systems and methods for treatment of prostate

Inventor: Dennis Giesing (Lee's Summit, MO)
Assignee: TARIS Biomedical LLC
A61M31/002A61K9/0034A61K31/7068A61K45/06A61M2205/04A61M2210/1085A61M2210/166
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Quick Facts
Patent No.
US 10,406,335
App. No.
15/473,437
Granted
Sep 10, 2019
Kind
B2
Abstract

Methods, devices, and medicaments that include a drug are provided for use in the treatment of the prostate by locally administering the drug into the bladder of a patient to achieve a sustained concentration of the drug in urine in the bladder sufficient to produce a therapeutic concentration of the drug in the prostate. The drug may be delivered into the bladder from an intravesical drug delivery device inserted into the bladder, wherein the device continuously releases the drug into the urine in the bladder over an extended period of hours or days.

Claims (25)

1. A medical device comprising:

a housing configured for intravesical insertion; and

a dosage form comprising gemcitabine,

wherein the housing holds the dosage form and is configured to release the gemcitabine into a bladder of a patient at a mean average amount from 1 mg/day to about 300 mg/day to provide an amount therapeutically effective for treatment of prostate cancer.

2. The device of claim 1 , wherein the gemcitabine contained in the housing is in a non-liquid form.

3. The device of claim 2 , wherein the non-liquid form is selected from the group consisting of tablets, granules, semisolids, capsules, and combinations thereof.

4. The device of claim 1 , wherein the housing is elastically deformable between a retention shape configured to retain the device in the bladder and a deployment shape for passage of the device through a urethra of the patient.

5. The device of claim 1 , which is configured to release from 1 mg/day to 100 mg/day of the gemcitabine for up to 7 days.

6. The device of claim 1 , which is configured to release from 20 mg/day to 300 mg/day of the gemcitabine for up to 7 days.

7. The device of claim 1 , wherein the device is configured to continuously release the gemcitabine into urine in the bladder over a sustained period.

8. The device of claim 7 , wherein the sustained period is at least 2 hours.

9. The device of claim 7 , wherein the sustained period is from 1 day to 14 days.

10. The device of claim 1 , wherein the device is configured to release the gemcitabine to achieve a sustained concentration of the gemcitabine in urine in the bladder sufficient to produce a therapeutic concentration of the gemcitabine in a prostate of the patient.

11. A medical device comprising:

a housing configured for intravesical insertion; and

a dosage form comprising gemcitabine,

wherein the housing holds the dosage form and is configured to release the gemcitabine at a mean average amount from 1 mg/day to about 300 mg/day to provide an amount effective to achieve a sustained concentration of the gemcitabine in urine in a bladder of a patient, the amount being sufficient to produce a therapeutic concentration of the gemcitabine in a prostate of the patient for treatment of prostate cancer.

12. The device of claim 11 , wherein the gemcitabine contained in the housing is in a non-liquid form.

13. The device of claim 12 , wherein the non-liquid form is selected from the group consisting of tablets, granules, semisolids, capsules, and combinations thereof.

14. The device of claim 11 , wherein the housing is elastically deformable between a retention shape configured to retain the device in the bladder and a deployment shape for passage of the device through a urethra of the patient.

15. The device of claim 11 , which is configured to release from 1 mg/day to 100 mg/day of the gemcitabine for up to 7 days.

16. The device of claim 11 , which is configured to release from 20 mg/day to 300 mg/day of the gemcitabine for up to 7 days.

17. The device of claim 11 , wherein the device is configured to continuously release the gemcitabine into the urine in the bladder over a sustained period.

18. The device of claim 17 , wherein the sustained period is at least 2 hours.

19. The device of claim 17 , wherein the sustained period is from 1 day to 14 days.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2018
From: GIESING, DENNIS
To: TARIS BIOMEDICAL, INC.
Reel/Frame 045535/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2018
From: LIRIS BIOMEDICAL, INC.
To: TARIS BIOMEDICAL LLC
Reel/Frame 045535/0528 →
CHANGE OF NAME Recorded Apr 13, 2018
From: TARIS BIOMEDICAL, INC.
To: LIRIS BIOMEDICAL, INC.
Reel/Frame 045947/0145 →
Continuity (4)
Division 14628874 · Feb 23, 2015
Continuation PCTUS2013057841 · Sep 3, 2013
Provisional Application 61696029 · Aug 31, 2012
Related Publication 20170203085A1 · Jul 20, 2017