MedPath

A Double-blind, Randomized, Multicenter, Placebo-controlled, Parallel Group, Dose Ranging Study to Assess the Efficacy, Safety, and Pharmacokinetics of an Oral Thrombopoietin Receptor Agonist SB-497115-GR Administered at 50, 75, and 100 mg to Cancer Patients receiving Multiple Cycles of Chemotherapy

Conditions
Treatment of chemotherapy induced thrombocytopenia with carboplatin and paclitaxel in advanced solid tumors.
MedDRA version: 6.1Level: HLTClassification code 10029105
Registration Number
EUCTR2004-000368-28-IT
Lead Sponsor
GLAXO SMITHKLINE
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
164
Inclusion Criteria

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: ;Secondary Objective: ;Primary end point(s):
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath