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Phase 3 N=234 Randomized Treatment

Romiplostim (AMG 531) Versus Medical Standard of Care for Immune (Idiopathic) Thrombocytopenic Purpura

Idiopathic Thrombocytopenic Purpura · Thrombocytopenia · Thrombocytopenia in Subjects With Immune (Idiopathic) Thrombocytopenic Purpura (ITP) · Thrombocytopenic Purpura

Enrolled (actual)
234
Serious AEs
28.0%
Results posted
Jul 2013
Primary outcome: Primary: Number of Participants With Splenectomy During 52-Week Treatment Period — 28; 14; 49; 143 Participants — p=<0.0001

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Medical Standard of Care for ITP (Drug); Romiplostim (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Amgen
Primary completion
Nov 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Splenectomy During 52-Week Treatment Period
28; 14; 49; 143 <0.0001 sig
PRIMARY
Number of Participants With Treatment Failure During 52-Week Treatment Period
23; 18; 54; 139 0.0005 sig
SECONDARY
Time to Splenectomy
NA; NA
SECONDARY
Percentage of Participants With Platelet Response
6.7; 3.9; 28.2; 75.8; 34.3; 73.0
SECONDARY
Change in ITP-PAQ Physical Health Domain of Symptoms
12.5; 16.0 0.0133 sig
SECONDARY
Change in ITP-PAQ Physical Health Domain of Fatigue
9.5; 11.2 0.3434
SECONDARY
Change in ITP-PAQ Physical Health Domain of Bother
13.0; 16.8 0.0076 sig
SECONDARY
Change in ITP-PAQ Physical Health Domain of Activity
8.2; 17.1 0.0246 sig

Summary

This is a phase 3b, multi-center, randomized, Standard of Care (SOC)-controlled, open-label, 52-week treatment study to compare romiplostim to medical SOC for Idiopathic Thrombocytopenia Purpura (ITP), with a 6-month Safety Follow-up. Patients randomized to romiplostim must complete the taper or discontinuation of medical SOC for ITP as soon as medically feasible after the initiation of romiplostim. After the completion or discontinuation of the study treatment period, any participant who does not transfer in to another romiplostim study will complete a 6-month Safety Follow-up period.

Eligibility Criteria

Inclusion Criteria

  • Subject is ≥ 18 years of age
  • Subject has a diagnosis of Idiopathic Thrombocytopenia Purpura (ITP) according to the American Society of Hematology (ASH) guidelines
  • If subject is > 60 years of age, subject has a written bone marrow biopsy report confirming the diagnosis of ITP
  • Subject has received at least 1 prior therapy for ITP
  • Subject has a platelet count < 50,000 or their platelet count falls to < 50,000 during or after a clinically-indicated taper or discontinuation of current ITP therapy
  • Before any study-specific procedure, the appropriate written informed consent must be obtained

Exclusion Criteria

  • Subject has had a splenectomy for any reason
  • Subject has an active malignancy
  • Subject has a history of cancer, other than basal cell carcinoma or cervical carcinoma in situ, with treatment or active disease within 5 years
  • Subject has a known history of bone marrow stem cell disorder
  • Subject has participated in any study evaluating polyethylene glycol-conjugated recombinant human megakaryocyte growth and development factor (PEG-rHuMGDF), recombinant human thrombopoietin (rHuTPO), AMG 531, or a thrombopoietic protein
  • Subject is receiving other investigational agents or procedures
  • Subject is currently enrolled in, or has completed within the last 30 days, another investigational device or drug study
  • Subject is pregnant or breast feeding
  • Subject is not using adequate contraceptive precautions
  • Subject has known sensitivity to any recombinant E. coli-derived product
  • Subject has any kind of disorder that compromises the ability of the subject to give written informed consent and does not have a legally acceptable representative
  • Subject has any kind of disorder that compromises the ability of the subject to comply with study procedures
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00415532). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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