Indirect Comparison Between Eltrombopag & Romiplostim

NCT ID: NCT01236014

Last Updated: 2017-06-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

1 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-08-31

Study Completion Date

2009-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

An indirect comparison to compare the efficacy of eltrombopag versus romiplostim

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

An indirect analysis was conducted to evaluate the relative efficacy of eltrombopag and romiplostim using placebo as a common comparator

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Thrombocytopaenia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Eltrombopag & standard of care

Eltrombopag

Intervention Type DRUG

Eltrombopag \& standard of care

Romiplostim & standard of care

Romiplostim

Intervention Type DRUG

Romiplostim \& standard of care

Standard of care

Placebo

Intervention Type DRUG

Placebo \& standard of care

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Eltrombopag

Eltrombopag \& standard of care

Intervention Type DRUG

Romiplostim

Romiplostim \& standard of care

Intervention Type DRUG

Placebo

Placebo \& standard of care

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adults with ITP
* Pre-specified treatment
* Prospective clinical studies with at least 10 patients

Exclusion Criteria

* Adults with ITP for other reasons
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

GlaxoSmithKline

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

114014

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Meta-analysis - Eltrombopag
NCT01235988 COMPLETED