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NCT02974855 · ClinicalTrials.gov registry record · Phase 2

PF-06741086 Multiple Dose Study in Severe Hemophilia

A Phase 2 study of Hemophilia A or B, sponsored by Pfizer.

Completed
Registry status
Phase 2
Development phase
27
Enrollment target
10
Study locations

NCT02974855 is a Phase 2 study of Hemophilia A or B that has completed, run by Pfizer. The registered enrollment target is 27 participants. The trial reports 10 study locations across 5 states.

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The verdict

NCT02974855, a Phase 2 study of Hemophilia A or B, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
27 participants
Enrollment target
10
Study locations

Study Summary

This study is designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of multiple subcutaneous and/or intravenous doses of PF-06741086 in subjects with severe hemophilia.

Conditions Studied

Interventions

  • BIOLOGICAL PF-06741086

Study Locations (10)

Other

  • Hospital Dr. Sotero del Rio - Santiago
  • Klinicki bolnicki centar Zagreb - Zagreb
  • Klinika Hematologii i Transplantologii Uniwersyteckie Centrum Kliniczne - Gdansk
  • UniversitatsSpital Zurich, Klinik fur Hamatologie - Zurich

Colorado

  • UC Denver Hemophilia and Thrombosis Center - Pharmacy - Aurora
  • UC Denver Hemophilia and Thrombosis Center - Aurora

Illinois

  • Pharmacy - Chicago
  • Rush University Medical Center - Chicago

Eastern Cape

  • Phoenix Pharma (Pty) Ltd - Port Elizabeth

Gauteng

  • Haemophilia Comprehensive Care Centre - Johannesburg

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2017-03-08
Est. Completion 2018-12-03
Phase Phase 2

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT02974855

The ClinicalTrials.gov registry entry for NCT02974855 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hemophilia A or B appearing as the primary indexed condition, and to 1 intervention - of which PF-06741086 is the first listed.

NCT02974855 reports 10 study locations spanning 5 distinct geographic areas - top geographies include Other, Colorado, Illinois.

Frequently Asked Questions

What is clinical trial NCT02974855 about?

NCT02974855 is a clinical study titled "PF-06741086 Multiple Dose Study in Severe Hemophilia". This study is designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of multiple subcutaneous and/or intravenous doses of PF-06741086 in subjects with severe hemophilia.

What is the current status of trial NCT02974855?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 27 participants. The study started on 2017-03-08. Estimated completion is 2018-12-03.

What conditions does trial NCT02974855 study?

This clinical trial studies the following conditions: Hemophilia A or B.

What interventions are being tested in trial NCT02974855?

The interventions under investigation include: PF-06741086 (BIOLOGICAL).

Who is sponsoring clinical trial NCT02974855?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02974855 being conducted?

This trial has 10 study locations across Colorado, Illinois, Eastern Cape, Gauteng. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.