We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Assessing the Pharmacokinetics of NKTR-118 in Subjects With Renal Impairment Compared to That in Subjects With Normal Renal Function

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01372826
First Posted: June 14, 2011
Last Update Posted: October 15, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
AstraZeneca
  Purpose
This study will be assessing the pharmacokinetics of NKTR-118 in subjects with renal impairment compared to that in subjects with normal renal function.

Condition Intervention Phase
Renal Impairment Drug: NKTR118 Group1 Drug: NKTR118 Group 2 Drug: NKTR118 Group3 Drug: NKTR118 Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: An Open-Label, Parallel-Group, Phase I Study to Compare the Pharmacokinetics of NKTR-118 Following a Single Oral Dose in Subjects With Renal Impairment and Subjects With Normal Renal Function

Resource links provided by NLM:


Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • To assess the pharmacokinetics of a single dose of NKTR-118 25 mg by assessment of area under the curve over the time (AUC) [ Time Frame: PK blood samples will be collected in treatment periods 1 and 2 at predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 h post-dose. ]
    Groups 1 (normal), 2 (moderate), 3 (severe), and for Group 4 (End-stage renal disease requiring hemodialysis)

  • To assess the pharmacokinetics of a single dose of NKTR-118 25 mg by assessment of maximum concentration (Cmax) [ Time Frame: PK blood samples will be collected in treatment periods 1 and 2 at predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 h post-dose. ]
    Groups 1 (normal), 2 (moderate), 3 (severe), and for Group 4 (End-stage renal disease requiring hemodialysis)


Secondary Outcome Measures:
  • To assess the safety and tolerability of NKTR-118 in subjects with renal impairment and normal renal function by assessing Adverse events. [ Time Frame: Duration Day -1 to follow-up at either visit 3 or 6 dependant on treatment ]
  • To assess the safety and tolerability of NKTR-118 in subjects with renal impairment and normal renal function by assessing vital signs [ Time Frame: Duration Day -1 to follow-up at either visit 3 or 6 dependant on treatment ]
  • To assess the safety and tolerability of NKTR-118 in subjects with renal impairment and normal renal function by assessing safety blood samples [ Time Frame: Duration Day -1 to follow-up at either visit 3 or 6 dependant on treatment ]

Enrollment: 32
Study Start Date: June 2011
Study Completion Date: November 2011
Primary Completion Date: October 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: NKTR118 Group1
Normal Renal Function
Drug: NKTR118 Group1
Oral dose, 25 mg
Experimental: NKTR118 Group 2
Moderate Renal Function
Drug: NKTR118 Group 2
Oral dose, 25 mg
Experimental: NKTR118 Group 3
Severe Renal Impairment
Drug: NKTR118 Group3
Oral dose, 25 mg
Experimental: NKTR118 Group 4
End-Stage Renal Disease
Drug: NKTR118
Oral dose, 25 mg

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Provision of signed written and dated informed consent prior to any study specific procedures.
  • Male or female volunteers aged 18 to 80 years (inclusive) having normal renal function, or suffering from moderate or severe renal impairment or ESRD.

Male subjects who are sexually active must be willing to use a barrier method of contraception (condom). Women must be of non-childbearing potential or, if of childbearing potential, must have a negative pregnancy test (at screening and at each admission) and be using a highly effective form of birth control for 3 months before enrollment and be willing to use a highly effective form of birth control during the study and until 3 months after their last dose of IP.

  • Have a BMI between 18 and 40 kg/m2 (inclusive) and weigh at least 50 kg.
  • Subjects must be able to understand and to comply with study procedures, restrictions and requirements.

Exclusion Criteria:

  • History of any clinically significant medical history which, in the opinion of the Investigator and Sponsor, may either put the subject at risk because of participation in the study, or influence the results, or the subject's ability to participate in the study.
  • History or presence of gastrointestinal hepatic or other condition known to interfere with disposition of the study drug (except for renal function impairment).
  • Subjects who have a functioning kidney transplant.
  • Acute illness, surgical procedures or trauma from within 2 weeks before enrollment until first administration of study drug
  • Known or suspected history of drug abuse as judged by the Investigator.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01372826


Locations
United States, California
Research Site
Anaheim, California, United States
United States, Florida
Research Site
Orlando, Florida, United States
United States, Kansas
Research Site
Overland Park, Kansas, United States
Sponsors and Collaborators
AstraZeneca
Investigators
Study Director: Mark Sostek, MD AstraZeneca
Principal Investigator: Thomas Marbury, MD Orlando Clinical Research Center US
  More Information

Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: AstraZeneca
ClinicalTrials.gov Identifier: NCT01372826     History of Changes
Other Study ID Numbers: D3820C00009
First Submitted: May 25, 2011
First Posted: June 14, 2011
Last Update Posted: October 15, 2014
Last Verified: October 2014

Keywords provided by AstraZeneca:
Phase 1
Pharmacokinetics
NKTR-118
renal impairment
parallel study
QTcF Interval
AUC(0-t)
Cmax
tmax

Additional relevant MeSH terms:
Renal Insufficiency
Kidney Diseases
Urologic Diseases
Naloxegol
Narcotic Antagonists
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents