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A Pharmacokinetic Study of CVX-096 (PF-04856883) in Healthy Volunteers

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ClinicalTrials.gov Identifier: NCT01637285
Recruitment Status : Completed
First Posted : July 11, 2012
Last Update Posted : July 31, 2015
Information provided by (Responsible Party):

Brief Summary:
The purpose of the study is to further evaluate the PK characteristics of PF-04856883.

Condition or disease Intervention/treatment Phase
Healthy Biological: PF-04856883 Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 49 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Official Title: A Phase 1, Randomized, Open-label, Parallel-group Study To Evaluate The Pharmacokinetics Of Pf-04856883 (Cvx-096) Following Subcutaneous Administration In Healthy Volunteers
Study Start Date : August 2012
Actual Primary Completion Date : January 2013
Actual Study Completion Date : January 2013

Arm Intervention/treatment
Experimental: PF-04856883 Treatment Arm 1 Biological: PF-04856883
Dose A

Experimental: PF-04856883 Treatment Arm 2 Biological: PF-04856883
Dose B

Experimental: PF-04856883 Treatment Arm 3 Biological: PF-04856883
Dose C

Experimental: PF-04856883 Treatment Arm 4 Biological: PF-04856883
Dose D

Primary Outcome Measures :
  1. PF-04856883 Pharmacokinetics including Cmax, Tmax, AUCo-infinity, AUClast, Cl/F, Vz/F and t1/2 [ Time Frame: 4 weeks ]

Secondary Outcome Measures :
  1. Number of subjects with AEs reported [ Time Frame: 4 weeks ]
  2. Number of subjects with abnormal physical examination findings [ Time Frame: 4 weeks ]
  3. Number of subjects with abnormal clinical laboratory results [ Time Frame: 4 weeks ]
  4. Number of subjects with abnormal ECGs [ Time Frame: 4 weeks ]
  5. Number of subjects with abnormal vital signs [ Time Frame: 4 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:


Exclusion Criteria:


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): NCT01637285

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United States, Connecticut
New Haven Clinical Research Unit
New Haven, Connecticut, United States, 06511
Sponsors and Collaborators
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Study Director: Pfizer CT.gov Call Center Pfizer
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Responsible Party: Pfizer
ClinicalTrials.gov Identifier: NCT01637285    
Other Study ID Numbers: B1111005
First Posted: July 11, 2012    Key Record Dates
Last Update Posted: July 31, 2015
Last Verified: July 2015