search
Back to results

Pharmacokinetic and Safety Study of OMS201 in Subjects Undergoing Ureteroscopic Treatment for Removal of Urinary Tract-Located Stones

Primary Purpose

Urinary Calculi, Urinary Stones, Urinary Tract Stones

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
OMS201
Vehicle
Sponsored by
Omeros Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Calculi focused on measuring Urinary Calculi, Urinary Stones, Urinary Tract Stones, Calculi

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subject is undergoing unilateral ureteroscopic removal of renal collecting system or ureteral stones located in the ureter with a maximum stone diameter of 12 mm, for which general anesthesia will be used.
  • Subject's physical examination is within normal limits or examination is clinically non-significant for purposes of the study as determined by the Investigator, and subject is in good general health.
  • Subject's laboratory evaluations are within normal limits or evaluations are clinically non-significant as determined by the Investigator.
  • Female subject of childbearing potential who is using an effective method of birth control within at least 14 days prior to surgery and has a negative pregnancy test.
  • Subject is at minimal risk from anesthesia and is classified according to the American Society of Anesthesiologists Physical Status Classification as either PS-1 or PS-2.
  • Subject's body mass index is between 19 and 35, inclusive, based on the Body Mass Index Table.

Exclusion Criteria:

  • Subject taking a prohibited medication.
  • Subject who has had a renal transplant, has a single kidney or has evidence of a compromised renal function as measured by abnormal serum creatinine, as judged by the Investigator, or who has evidence of urinary tract infection, or has prior history of open or laparoscopic surgery, or any history of an ureteral stricture.
  • Subject who has congenital anomalies that would engender an increased procedural safety risk such as ureteropelvic junction obstruction resulting in severely dilated renal pelvis, duplicated urinary collecting system, horseshoe kidney or vascular anomalies such as renal arteriovenous fistulas or papillary necrosis.
  • Subject has bilateral renal or ureteral stones requiring concurrent ureteroscopic removal.
  • Subject with clinically significant hypotension at Screening.
  • Subject who has a present condition or history of any clinically significant uncontrolled gastrointestinal, cardiovascular, hepatic, renal, hematological, endocrine, neurological, psychiatric, connective tissue, respiratory or other medical disorder as determined by the Investigator.
  • Subject on chronic diuretic use.
  • Subject who has taken or used an investigational drug or device within 30 days prior to the day of surgery.

Sites / Locations

  • UC Irvine Medical Center
  • University of Texas Southwestern

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Drug

Vehicle

Outcomes

Primary Outcome Measures

Pharmacokinetic

Secondary Outcome Measures

Safety

Full Information

First Posted
December 26, 2007
Last Updated
April 28, 2010
Sponsor
Omeros Corporation
search

1. Study Identification

Unique Protocol Identification Number
NCT00599664
Brief Title
Pharmacokinetic and Safety Study of OMS201 in Subjects Undergoing Ureteroscopic Treatment for Removal of Urinary Tract-Located Stones
Official Title
Double-Blind, Placebo-Controlled, Two-Center, Pharmacokinetic Study Evaluating the Systemic Absorption and Safety of OMS201 in Subjects Undergoing Ureteroscopic Treatment of Unilateral Ureteral- or Renal Collecting System-Located Stones
Study Type
Interventional

2. Study Status

Record Verification Date
April 2010
Overall Recruitment Status
Completed
Study Start Date
December 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Omeros Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Evaluate the safety and systemic absorption of OMS201 following exposure during ureteroscopy.
Detailed Description
OMS201 is being developed to facilitate endoscopy of the ureters and to reduce postoperative discomfort, such as pain, frequency, urgency and/or difficult urination following endoscopic surgery to remove a urinary tract stone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Calculi, Urinary Stones, Urinary Tract Stones
Keywords
Urinary Calculi, Urinary Stones, Urinary Tract Stones, Calculi

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Drug
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Vehicle
Intervention Type
Drug
Intervention Name(s)
OMS201
Intervention Description
OMS201 irrigation solution during surgery
Intervention Type
Drug
Intervention Name(s)
Vehicle
Intervention Description
Vehicle irrigation solution during surgery
Primary Outcome Measure Information:
Title
Pharmacokinetic
Time Frame
Day of Surgery
Secondary Outcome Measure Information:
Title
Safety
Time Frame
Day 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject is undergoing unilateral ureteroscopic removal of renal collecting system or ureteral stones located in the ureter with a maximum stone diameter of 12 mm, for which general anesthesia will be used. Subject's physical examination is within normal limits or examination is clinically non-significant for purposes of the study as determined by the Investigator, and subject is in good general health. Subject's laboratory evaluations are within normal limits or evaluations are clinically non-significant as determined by the Investigator. Female subject of childbearing potential who is using an effective method of birth control within at least 14 days prior to surgery and has a negative pregnancy test. Subject is at minimal risk from anesthesia and is classified according to the American Society of Anesthesiologists Physical Status Classification as either PS-1 or PS-2. Subject's body mass index is between 19 and 35, inclusive, based on the Body Mass Index Table. Exclusion Criteria: Subject taking a prohibited medication. Subject who has had a renal transplant, has a single kidney or has evidence of a compromised renal function as measured by abnormal serum creatinine, as judged by the Investigator, or who has evidence of urinary tract infection, or has prior history of open or laparoscopic surgery, or any history of an ureteral stricture. Subject who has congenital anomalies that would engender an increased procedural safety risk such as ureteropelvic junction obstruction resulting in severely dilated renal pelvis, duplicated urinary collecting system, horseshoe kidney or vascular anomalies such as renal arteriovenous fistulas or papillary necrosis. Subject has bilateral renal or ureteral stones requiring concurrent ureteroscopic removal. Subject with clinically significant hypotension at Screening. Subject who has a present condition or history of any clinically significant uncontrolled gastrointestinal, cardiovascular, hepatic, renal, hematological, endocrine, neurological, psychiatric, connective tissue, respiratory or other medical disorder as determined by the Investigator. Subject on chronic diuretic use. Subject who has taken or used an investigational drug or device within 30 days prior to the day of surgery.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott Houston
Organizational Affiliation
Omeros Corporation
Official's Role
Study Director
Facility Information:
Facility Name
UC Irvine Medical Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
University of Texas Southwestern
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Pharmacokinetic and Safety Study of OMS201 in Subjects Undergoing Ureteroscopic Treatment for Removal of Urinary Tract-Located Stones

We'll reach out to this number within 24 hrs