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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01710020
Other study ID # A3921004
Secondary ID
Status Completed
Phase Phase 1
First received October 16, 2012
Last updated November 19, 2012
Start date February 2003
Est. completion date June 2003

Study information

Verified date November 2012
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

There were 2 study periods in this study. In the Period 1, CP-690,550 was to be administered approximately 1 to 2 hours following hemodialysis. If significant non-renal clearance of the drug occurred such that dialyzability of CP-690,550 could not be assessed in Period 1, a second period (Period 2) will be conducted. In Period 2, a single dose of drug will be administered approximately 4 hours prior to hemodialysis.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date June 2003
Est. primary completion date June 2003
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Subjects with end-stage renal disease

- Subjects need hemodialysis 3 times weekly

Exclusion Criteria:

- Subjects with evidence or history of clinically significant disease, excluding those common for subjects with End-Stage Renal Disease (ESRD).

- Subjects with any condition possibly affecting drug absorption.

- Subjects with malignancies with the exception of adequately treated basal cell carcinoma of the skin.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science


Intervention

Drug:
CP-690,550
CP-690,550 10 mg oral powder for constitution

Locations

Country Name City State
United States Pfizer Investigational Site Minneapolis Minnesota
United States Pfizer Investigational Site Orlando Florida

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Overall Dialyser Clearance (CL HD) Dialyser clearance was calculated as amount of drug in dialysate collected over a period of time (AHD) divided by the product of fraction unbound of drug in plasma (fu), corresponding mid-time plasma concentration of drug (Cmid), and duration of dialysate collection period (tm). CL HD = AHD/(fu*Cmid*tm). 0 to 4 hrs during hemodialysis started 4 hrs post-dose in Period 2 No
Other Dialyser Clearance (CL HD) From 3 to 3.5 Hour Dialyser clearance was calculated as amount of drug in dialysate collected over a period of time (AHD) divided by the product of fraction unbound of drug in plasma (fu), corresponding mid-time plasma concentration of drug (Cmid), and duration of dialysate collection period (tm). CL HD = AHD/(fu*Cmid*tm). 3 to 3.5 hrs during hemodialysis started 4 hrs post-dose in Period 2 No
Primary Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0 - 8)] AUC (0 - 8)= Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0 - 8). It is obtained from AUC (0 - t) plus AUC (t - 8). 0 (pre-dose), 0.25, 0.5, 1, 2, 3, 4, 8, 12, 16, 24 hours (hrs) post-dose in Period 1 No
Primary Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) Area under the plasma concentration time-curve from zero to the last measured concentration (AUClast) 0 (pre-dose), 0.25, 0.5, 1, 2, 3, 4, 8, 12, 16, 24 hrs post-dose in Period 1 No
Primary Maximum Observed Plasma Concentration (Cmax) 0 (pre-dose), 0.25, 0.5, 1, 2, 3, 4, 8, 12, 16, 24 hrs post-dose in Period 1 No
Primary Time to Reach Maximum Observed Plasma Concentration (Tmax) 0 (pre-dose), 0.25, 0.5, 1, 2, 3, 4, 8, 12, 16, 24 hrs post-dose in Period 1 No
Primary Plasma Decay Half-Life (t1/2) Plasma decay half-life is the time measured for the plasma concentration to decrease by one half. 0 (pre-dose), 0.25, 0.5, 1, 2, 3, 4, 8, 12, 16, 24 hrs post-dose in Period 1 No
Primary Oral Clearance (CLpo) Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes. Drug clearance is a quantitative measure of the rate at which a drug substance is removed from the blood. It was calculated by dividing given dose of drug with AUC. 0 (pre-dose), 0.25, 0.5, 1, 2, 3, 4, 8, 12, 16, 24 hrs post-dose in Period 1 No
Primary Dialyser Clearance (CL HD) From 0 to 1 Hour Dialyser clearance was calculated as amount of drug in dialysate collected over a period of time (AHD) divided (/) by the product of fraction unbound of drug in plasma (fu), corresponding mid-time plasma concentration of drug (Cmid), and duration of dialysate collection period (tm). CL HD = AHD/(fu*Cmid*tm). 0 to 1 hrs during hemodialysis started 4 hrs post-dose in Period 2 No
Primary Dialyser Clearance (CL HD) From 1 to 2 Hour Dialyser clearance was calculated as amount of drug in dialysate collected over a period of time (AHD) divided by the product of fraction unbound of drug in plasma (fu), corresponding mid-time plasma concentration of drug (Cmid), and duration of dialysate collection period (tm). CL HD = AHD/(fu*Cmid*tm). 1 to 2 hrs during hemodialysis started 4 hrs post-dose in Period 2 No
Primary Dialyser Clearance (CL HD) From 2 to 3 Hour Dialyser clearance was calculated as amount of drug in dialysate collected over a period of time (AHD) divided by the product of fraction unbound of drug in plasma (fu), corresponding mid-time plasma concentration of drug (Cmid), and duration of dialysate collection period (tm). CL HD = AHD/(fu*Cmid*tm). 2 to 3 hrs during hemodialysis started 4 hrs post-dose in Period 2 No
Primary Dialyser Clearance (CL HD) From 3 to 4 Hour Dialyser clearance was calculated as amount of drug in dialysate collected over a period of time (AHD) divided by the product of fraction unbound of drug in plasma (fu), corresponding mid-time plasma concentration of drug (Cmid), and duration of dialysate collection period (tm). CL HD = AHD/(fu*Cmid*tm). 3 to 4 hrs during hemodialysis started 4 hrs post-dose in Period 2 No
Secondary Fraction of Unbound Drug (fu) Fraction of unbound drug (fu) is defined as the ratio of unbound drug concentration to the total drug concentration. 2 hours post-dose in Period 1 No
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