Trial record 5 of 330 for:
"Myelofibrosis"
Oral Pacritinib Versus Best Available Therapy to Treat Myelofibrosis
This study is currently recruiting participants.
Verified April 2013 by Cell Therapeutics
Sponsor:
Cell Therapeutics
Information provided by (Responsible Party):
Cell Therapeutics
ClinicalTrials.gov Identifier:
NCT01773187
First received: January 18, 2013
Last updated: April 18, 2013
Last verified: April 2013
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The primary hypothesis of the study is that treatment with pacritinib results in a greater proportion of patients achieving ≥ 35% reduction in spleen volume from baseline to Week 24 than treatment with BAT.
| Condition | Intervention | Phase |
|---|---|---|
|
Primary Myelofibrosis Post-polycythemia Vera Myelofibrosis Post-essential Thrombocythemia Myelofibrosis |
Drug: Pacritinib Drug: Best Available Therapy |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Randomized Controlled Phase 3 Study of Oral Pacritinib Versus Best Available Therapy in Patients With Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis |
Resource links provided by NLM:
Genetics Home Reference related topics:
essential thrombocythemia
polycythemia vera
primary myelofibrosis
U.S. FDA Resources
Further study details as provided by Cell Therapeutics:
Primary Outcome Measures:
- Efficacy [ Time Frame: Baseline to Week 24 ] [ Designated as safety issue: No ]To compare the efficacy of pacritinib with that of best available therapy (BAT) in patients with primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (PPV-MF), or post-essential thrombocythemia myelofibrosis (PET-MF); the efficacy measure for this analysis is the proportion of patients achieving a ≥ 35% reduction in spleen volume from baseline to week 24 by magnetic resonance imaging (MRI) or computed tomography (CT)
Secondary Outcome Measures:
- Symptomatic Efficacy [ Time Frame: Baseline to week 24 ] [ Designated as safety issue: No ]To compare pacritinib with best available therapy with respect to the proportion of patients with >= 50% reduction in total score from baseline to week 24 on the Myeloproliferative Neoplasm Symptom Assessment Form (MPN-SAF TSS)
| Estimated Enrollment: | 270 |
| Study Start Date: | December 2012 |
| Estimated Study Completion Date: | August 2017 |
| Estimated Primary Completion Date: | August 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Pacritinib
Pacritinib 400 mg taken orally, once daily
|
Drug: Pacritinib |
|
Active Comparator: Best Available Therapy
BAT includes any physician-selected treatment for PMF, PPV-MF, or PET-MF with the exclusion of JAK inhibitors (inhibitors of Janus kinases). For example, BAT may include hydroxyurea, glucocorticoids, erythropoietic agents, immunomodulatory agents, mercaptopurine, danazol, interferons, cytarabine, melphalan, or other agents.
|
Drug: Best Available Therapy |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Intermediate -1 or -2 or high-risk Myelofibrosis (per Passamonti et al 2010)
- Palpable splenomegaly ≥ 5 cm on physical examination
- Score ≥ 3 for at least two symptoms on the MPN-SAF TSS or score ≥ 4 for at least one symptom on MPN-SAF TSS other than fatigue
- Patients who are platelet or red blood cell transfusion-dependent are eligible
- Adequate white blood cell counts (with low blast counts), liver function, and renal function
- No spleen radiation therapy for 6-12 months
- Last therapy for myelofibrosis was 2-4 weeks ago, including any erythropoietic or thrombopoietic agent
- Not pregnant, not lactating, and agree to use effective birth control
Exclusion Criteria:
- Prior treatment with a JAK2 inhibitor
- History of (or plans to undergo) spleen removal surgery or allogeneic stem cell transplant
- Ongoing gastrointestinal medical condition such as Crohn's disease, Inflammatory bowel disease, chronic diarrhea, or constipation
- Cardiovascular disease, including recent history or currently clinically symptomatic and uncontrolled: congestive heart failure, arrhythmia, angina, QTc prolongation or other QTc risk factors, myocardial infarction
- Other malignancy within last 3 years other than certain limited skin, cervical, prostate, breast, or bladder cancers
- Other ongoing, uncontrolled illnesses (including HIV infection and active hepatitis A, B, or C), psychiatric disorder, or social situation that would prevent good care on this study
- Life expectancy < 6 months
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01773187
Contacts
| Contact: James Dean, MD, PhD | 206.272.4679 | jdean@ctiseattle.com |
| Contact: Jennifer Callahan, MAS | 206.272.4683 | jcallahan@ctiseattle.com |
Locations
| United States, New Jersey | |
| CTI Investigational Site 10001 | Recruiting |
| Morristown, New Jersey, United States, 07962 | |
| Australia | |
| CTI Investigational Site 61001 | Recruiting |
| Coffs Harbour, Australia | |
| CTI Investigational Site 61005 | Recruiting |
| Geelong, Australia | |
| CTI Investigational Site 61004 | Recruiting |
| Hobart, Australia | |
| CTI Investigational Site 61002 | Recruiting |
| Milton, Australia | |
| Belgium | |
| CTI Investigational Site 32002 | Recruiting |
| Antwerp, Belgium | |
| CTI Investigational Site 32003 | Recruiting |
| Antwerp, Belgium | |
| CTI Investigational Site 32001 | Recruiting |
| Brugge, Belgium | |
| Czech Republic | |
| CTI Investigational Site 42002 | Recruiting |
| Plzen, Czech Republic | |
| Netherlands | |
| CTI Investigational Site 31001 | Recruiting |
| Amsterdam, Netherlands | |
| New Zealand | |
| CTI Investigational Site 64001 | Recruiting |
| Christchurch, New Zealand | |
| CTI Investigational Site 64002 | Recruiting |
| Hamilton, New Zealand | |
| CTI Investigational Site 64003 | Recruiting |
| Takapuna, New Zealand | |
Sponsors and Collaborators
Cell Therapeutics
Investigators
| Study Director: | James Dean, MD, PhD | Cell Therapeutics |
More Information
No publications provided
| Responsible Party: | Cell Therapeutics |
| ClinicalTrials.gov Identifier: | NCT01773187 History of Changes |
| Other Study ID Numbers: | PERSIST-1 (PAC325) |
| Study First Received: | January 18, 2013 |
| Last Updated: | April 18, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Cell Therapeutics:
|
Myelofibrosis Post-Polycythemia Vera Myelofibrosis Post-Essential Thrombocythemia Myelofibrosis Primary Myelofibrosis Polycythemia Polycythemia Vera Thrombocythemia, Essential Thrombocythemia Myeloproliferative Disorders Bone Marrow Disease Hematologic Diseases Blood Platelet Disorders |
Hemorrhagic Disorders Splenomegaly Pacritinib MPN-SAF MPN-SAF TSS Anemia Myeloproliferative Myeloproliferative Neoplasm Spleen Spleen volume Thrombocytopenia SB1518 |
Additional relevant MeSH terms:
|
Primary Myelofibrosis Polycythemia Polycythemia Vera Thrombocythemia, Essential Thrombocytosis Myeloproliferative Disorders |
Bone Marrow Diseases Hematologic Diseases Blood Coagulation Disorders Blood Platelet Disorders Hemorrhagic Disorders |
ClinicalTrials.gov processed this record on May 16, 2013