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Pharmacokinetics And Tolerability Of Subcutaneous Administration Of PF 04236921 In Healthy Volunteers

Pfizer logo

Pfizer

Status and phase

Completed
Phase 1

Conditions

Healthy

Treatments

Drug: PF-04236921

Study type

Interventional

Funder types

Industry

Identifiers

NCT01166555
EudraCT 2010-019770-32
B0151004

Details and patient eligibility

About

This study will evaluate the safety, tolerability, and pharmacokinetics of PF-04236921 administered as a single subcutaneous dose in healthy volunteers.

Full description

Tolerability and Pharmacokinetics of subcutaneously administered dose of PF-04236921 in healthy volunteers

Enrollment

10 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy males between 18-55 years, inclusive.
  • Healthy females of non-childbearing potential between 18 and 55 years, inclusive.

Exclusion criteria

  • Evidence or history of clinically significant disease.
  • Females of childbearing potential.

Trial design

10 participants in 1 patient group

1
Experimental group
Treatment:
Drug: PF-04236921

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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