A Phase 1, Within Cohort, Randomized, Double Blind, Third-Party Open, Placebo-Controlled, Single- And Multiple Dose Escalation, Parallel Group Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of Pf-04965842 In Healthy Western and Japanese Subjects

Trial Profile

A Phase 1, Within Cohort, Randomized, Double Blind, Third-Party Open, Placebo-Controlled, Single- And Multiple Dose Escalation, Parallel Group Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of Pf-04965842 In Healthy Western and Japanese Subjects

Completed
Phase of Trial: Phase I

Latest Information Update: 09 Jul 2014

At a glance

  • Drugs PF 4965842 (Primary)
  • Indications Lupus vulgaris; Rheumatoid arthritis
  • Focus Adverse reactions; First in man; Pharmacodynamics
  • Sponsors Pfizer
  • Most Recent Events

    • 19 Jun 2014 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
    • 22 May 2014 Planned End Date changed from 1 Apr 2014 to 1 Jun 2014 as reported by ClinicalTrials.gov.
    • 24 Feb 2014 Planned number of patients changed from 64 to 72, as per ClinicalTrials.gov record.
Restricted Access

Oops, it looks like you don’t have a valid subscription to this content. To gain full access to the content and functionality of the AdisInsight database try one of the following.

  • with a username/password associated to an account with a valid subscription
  • Contact your organization’s admin about adding this content to your AdisInsight subscription
  • Request a trial

If you are a subscriber to this content then contact us at AsktheExpert.AdisInsight@springer.com so we can help.

Back to top