Evaluating pacritinib for patients with myelofibrosis and low platelet counts
Official title: A Randomized, Controlled Phase 3 Study of Pacritinib Versus Physician's Choice in Patients with Primary Myelofibrosis, Post Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis with Severe Thrombocytopenia (Platelet Count <50,000/μL)(PACIFICA)
Run by Swedish Orphan Biovitrum · NCT03165734 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing if a new drug called pacritinib can help people with myelofibrosis and low platelet counts feel better compared to standard treatments chosen by their doctors.
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 399 (estimated) |
| Sponsor | Swedish Orphan Biovitrum Industry-sponsored |
| Drugs / interventions | pacritinib, ruxolitinib, fedratinib, momelotinib |
| Locations | 185 sites (Birmingham, Alabama and 184 other locations) |
| Trial ID | NCT03165734 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older with a diagnosis of primary myelofibrosis or related conditions and a platelet count of less than 50,000/μL.
✕Probably not a fit
Patients who have previously been treated with more than one JAK2 inhibitor may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This phase 3 study compares the efficacy of pacritinib, administered at a dose of 200 mg twice daily, against physician's choice therapy in patients suffering from primary myelofibrosis, post-polycythemia vera myelofibrosis, or post-essential thrombocythemia myelofibrosis who have severe thrombocytopenia. Approximately 399 patients will be enrolled and randomized in a 2:1 ratio to receive either pacritinib or a selected P/C therapy, which includes corticosteroids, hydroxyurea, danazol, or low-dose ruxolitinib. The study aims to determine the effectiveness of pacritinib in improving patient outcomes compared to standard treatment options.
Why it matters
Potential benefit: If successful, this treatment could provide a new effective option for patients with myelofibrosis who have low platelet counts.
How similar studies have gone: Other studies have shown promising results with similar approaches, particularly in the use of pacritinib for myelofibrosis treatment.
Who can join: the full rules
Show full inclusion / exclusion criteria
Diagnosis and Inclusion Criteria 1. Primary MF, post-polycythemia vera MF, or post-essential thrombocythemia MF (as defined by Tefferi and Vardiman 2008 2. Platelet count of \<50,000/μL at Screening (Day -35 to Day -3) 3. Dynamic International Prognostic Scoring System Intermediate-1, Intermediate-2, or High-Risk (Passamonti et al 2010 4. Palpable splenomegaly ≥5 cm below the lower costal margin (LCM) in the midclavicular line as assessed by physical examination 5. TSS of ≥10 on the MPN-SAF TSS 2.0 or a single symptom score of ≥5 or two symptoms of ≥3, including only the symptoms of left upper quadrant pain, bone pain, itching, or night sweats.The TSS criteria need only to be met on a single day. 6. Age ≥18 years 7. Eastern Cooperative Oncology Group performance status 0 to 2 8. Peripheral blast count of \<10% throughout the Screening period prior to randomization 9. Absolute neutrophil count of ≥500/µL 10. Left ventricular cardiac ejection fraction of ≥50% by echocardiogram or multigated acquisition scan 11. Adequate liver and renal function, defined by liver transaminases (aspartate aminotransferase \[AST\]/serum glutamic-oxaloacetic transaminase \[SGOT\] and alanine aminotransferase \[ALT\]/serum glutamic pyruvic transaminase \[SGPT\]) ≤3 × the upper limit of normal (ULN) (AST/ALT ≤5 × ULN if transaminase elevation is related to MF), total bilirubin ≤4 x ULN (in cases where total bilirubin is elevated, direct bilirubin ≤4 × ULN, is required) and creatinine ≤2.5 mg/dL 12. Adequate coagulation defined by prothrombin time/international normalized ratio and partial thromboplastin time ≤1.5 × ULN 13. If fertile, willing to use highly effective birth control methods during the study 14. Willing to undergo and able to tolerate frequent MRI or CT scan assessments during the study 15. Able to understand and willing to complete symptom assessments using a patient-reported outcome instrument 16. Provision of signed informed consent Exclusion Criteria 1. Life expectancy \<6 months 2. Completed allogeneic stem cell transplant (allo-SCT) or are eligible for and willing to complete other approved available therapy including allogeneic stem cell 3. History of splenectomy or planning to undergo splenectomy 4. Splenic irradiation within the last 6 months 5. Previously treated with pacritinib 6. Treatment with any MF-directed therapy within 14 days prior to treatment Day 1 7. Prior treatment with more than one JAK2 inhibitor 8. Prior treatment with with ruxolitinib, if BOTH of the following conditions are met: i. exposure to higher-dose ruxolitinib (\>10 mg daily) within 120 days prior to treatment Day 1 AND ii. total duration of treatment with higher-dose ruxolitinib (\>10 mg daily) was \>90 days, from first to last exposure (i.e., this 90-day period starts on the date of first administration of ruxolitinib at a total daily dose of \>10 mg and continues for 90 calendar days, regardless of whether higher-dose ruxolitinib is administered continuously or intermittently). 9. Prior treatment with any JAK2 inhibitor other than ruxolitinib, irrespective of dose, with a duration of \>90 days. The 90-day period starts on the date of first administration of JAK2 inhibitor therapy and continues for 90 calendar days, regardless of whether therapy is administered continuously or intermittently. 10. Treatment with an experimental therapy, including MF-directed experimental therapies within 28 days prior to treatment Day 1 11. Systemic treatment with a strong CYP 3A4 inhibitor or a strong CYP 3A4 inducer within 14 days prior to treatment Day 1. Shorter washout periods may be permitted with approval of the Medical Monitor, provided that the washout period is at least five half-lives of the drug prior to treatment Day 1 12. Significant recent bleeding history defined as National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) grade ≥2 within 3 months prior to treatment Day 1, unless precipitated by an inciting event (eg, surgery, trauma, or injury) 13. Systemic treatment with medications that increase the risk of bleeding, including anticoagulants, antiplatelet agents (except for aspirin dosages of ≤100 mg per day),and daily use of cyclooxygenase-1 (COX-1) inhibiting non-steroidal anti-inflammatory drugs (NSAIDs) within 14 days prior to treatment Day 1. Treatment with systemic anti-vascular endothelial growth factor (anti-VEGF) agents within 28 days prior to treatment Day 1. 14. Systemic treatment with medications that can prolong the QT interval within 14 days prior to treatment Day 1. Shorter washout periods may be permitted with approval of the Medical Monitor, provided that the washout period is at least five half-lives of the drug prior to treatment Day 1 15. Any history of CTCAE grade ≥2 non-dysrhythmia cardiac conditions within 6 months prior to treatment Day 1. Patients with asymptomatic grade 2 non-dysrhythmia cardiovascular conditions may be considered for inclusion, with the approval of the Medical Monitor, if stable and unlikely to affect patient safety. 16. Any history of CTCAE grade ≥2 cardiac dysrhythmias within 6 months prior to treatment Day 1. Patients with non-corrected QT interval CTCAE grade 2 cardiac dysrhythmias may be considered for inclusion, with the approval of the Medical Monitor, if the dysrhythmias are stable, asymptomatic, and unlikely to affect patient safety. 17. QT corrected by the Fridericia method (QTcF) prolongation \>450 ms or other factors that increase the risk for QT interval prolongation (eg, hypokalemia \[defined as serum potassium \<3.0 mEq/L that is persistent and refractory to correction\], or history of long QT interval syndrome). 18. New York Heart Association Class II, III, or IV congestive heart failure 19. Any active gastrointestinal or metabolic condition that could interfere with absorption of oral medication 20. Active or uncontrolled inflammatory or chronic functional bowel disorder such as Crohn's Disease, inflammatory bowel disease, chronic diarrhea, or chronic constipation 21. Other malignancy within 3 years prior to treatment Day 1. The following patients may be eligible despite having had a malignancy within the prior 3 years: patients with curatively treated squamous or basal cell carcinoma of the skin; patients with curatively treated non-invasive cancers; patients with organ-confined prostate cancer with prostate specific antigen (PSA) \<20 ng/mL and National Comprehensive Cancer Network risk of Very Low, Low, or Favorable Intermediate; and patients with curatively treated non-metastatic prostate cancer with negative PSA. 22. Uncontrolled intercurrent illness, including, but not limited to, ongoing active infection, psychiatric illness, or social situation that, in the judgment of the treating physician, would limit compliance with study requirements 23. Known seropositivity for human immunodeficiency (HIV) virus. For patients in France, Czech Republic, and Italy only: testing for HIV is required during Screening. 24. Known active hepatitis A, B, or C virus infection. For patients in France, Czech Republic and Italy only: testing for hepatitis B and C is required during Screening. 25. Women who are pregnant or lactating 26. Concurrent enrollment in another interventional trial 27. Severe thrombocytopenia due to vitamin B12 deficiency, folate deficiency, or viral infection in the opinion of the investigator 28. Known hypersensitivity to pacritinib or any of the following inactive ingredients: microcrystalline cellulose, polyethylene glycol, and magnesium stearate; any contraindication to the "physician's choice" medicinal product selected by the investigator to be used as the comparator or to loperamide or equivalent antidiarrheal medication 29. Persons deprived of their liberty by a judicial or administrative decision 30. Persons subject to legal protection measures or unable to express their consent 31. Temporarily incapacitated persons
Where it's running
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Westmead Hospital
Sydney, New South Wales, Australia Recruiting -
Alfred Hospital, Malignant Hematology and Stem Cell Transplantation Service
Melbourne, Victoria, Australia Recruiting -
The Perth Blood Institute
Perth, Western Australia, Australia Recruiting -
Republican Research Center for Radiation Medicine and Human Ecology
Gomel, Belarus Recruiting -
Minsk Scientific and Practical Center of Surgery, Transplantology and Hematology
Minsk, Belarus Recruiting -
University Clinical Centre of the Republic of Srpska
Banja Luka, Bosnia and Herzegovina Recruiting
Show 44 more locations
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University Clinical Center of Sarajevo
Sarajevo, Bosnia and Herzegovina Recruiting -
University Multiprofile Hospital for Active Treatment "Dr. Georgi Stranski"
Pleven, Bulgaria Recruiting -
University Multiprofile Hospital for Active Treatment "Sveti Georgi", Plovdiv
Plovdiv, Bulgaria Recruiting -
Multiprofile Hospital for Active Treatment - Sofia, part of Military Medical Academy
Sofia, Bulgaria Recruiting -
Multiprofile Hospital for Active Treatment "Sveta Marina"
Varna, Bulgaria Recruiting -
Tom Baker Cancer Center, Internal Medicine/Hematology
Calgary, Alberta, Canada Recruiting -
Providence Hematology - Vancouver
Vancouver, British Columbia, Canada Recruiting -
Eastern Regional Health Authority
Saint John's, Newfoundland and Labrador, Canada Recruiting -
Nova Scotia Health Authority, Centre for Clinical Research
Halifax, Nova Scotia, Canada Recruiting -
Princess Margaret Cancer Centre
Toronto, Ontario, Canada Recruiting -
Jewish General Hospital; Clinical Research Unit
Montreal, Quebec, Canada Recruiting -
University Hospital Brno
Brno, Czechia Recruiting -
University Hospital Olomouc
Olomouc, Czechia Recruiting -
University Hospital Plzen
Pilsen, Czechia Recruiting -
University Hospital Kralovske Vinohrady, Clinic of Internal Hematology
Prague, Czechia Recruiting -
CHU Hôpital Amiens Sud
Amiens, France Recruiting -
La Conception Hospital
Marseille, France Recruiting -
CHU de Nimes - Hopital Universitaire Caremeau
Nîmes, France Recruiting -
Hôpital Saint-Louis
Paris, France Recruiting -
CHU Hopitaux de Bordeaux - Hôpital Haut-Lévêque
Pessac, France Recruiting -
Centre Hospitalier Lyon-Sud
Pierre Benite, France Recruiting -
University Hospital Center of Poitiers
Poitiers, France Recruiting -
JSC K. Eristavi National Center For Experimental and Clinical Surgery
Tbilisi, Georgia Recruiting -
Tbilisi State Medical University and Ingorokva High Medical Technology University Clinic LLC
Tbilisi, Georgia Recruiting -
University of Debrecen Clinical Center (Debreceni Egyetem Klinikai Központ)
Debrecen, Hungary Recruiting -
Somogy Megyei Kaposi Mór Oktató Kórház
Kaposvár, Hungary Recruiting -
Szabolcs-Szatmar-Bereg County Hospitals and University Teaching Hospital, Department of Hematology
Nyíregyháza, Hungary Recruiting -
Gauhati Medical College and Hospital
Guwahati, Assam, India Recruiting -
Sahyadri Super Speciality Hospital
Pune, Maharashtra, India Recruiting -
Shri Ram Cancer Centre, Mahatma Gandhi Medical College & Hospital
Jaipur, Rajasthan, India Recruiting -
Tata Medical Center
Kolkata, West Bengal, India Recruiting -
St. John's Medical College Hospital
Bengaluru, India Recruiting -
Lady Davis Carmel Medical Center, Department of Hematology,
Haifa, Israel Recruiting -
Hadassah Medical Center, Department of Hematology,
Jerusalem, Israel Recruiting -
Meir Medical Center, Hematology Institute and Blood Bank
Kfar Saba, Israel Recruiting -
Rabin Medical Center, Clinic for Myeloproliferative Disorders
Petah-Tikva, Israel Recruiting -
The Tel Aviv Sourasky Medical Center, Department of Internal Medicine
Tel Aviv, Israel Recruiting -
Cancer Institute "Giovanni Paolo II", IRCCS
Bari, Italy Recruiting -
Polyclinic S. Orsola-Malpighi
Bologna, Italy Recruiting -
ASST Spedali Civili Brescia, Hematology Unit
Brescia, Italy Recruiting -
Azienda Ospedaliero-Universitaria Careggi
Florence, Italy Recruiting -
Scientific Institute of Romagna for the Study and Treatment of Cancer (IRST), IRCCS
Forlì, Italy Recruiting -
Maggiore Polyclinic Hospital, Fondazione IRCCS Ca' Granda
Milan, Italy Recruiting -
ASST Monza - Ospedale San Gerardo
Monza, Italy Recruiting
+135 more sites. See ClinicalTrials.gov for the full list.
Study contacts
- Study coordinator: Study Contact
- Email: medical.info@sobi.com
- Phone: +4686972000
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
MPN PROGRESSion Registry — tracking symptoms, treatments, and disease progression in people with MPNs.
Track long-term symptoms, treatments, and disease progression in adults with myeloproliferative neoplasms to see how these conditions evolve over time.
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Combining Momelotinib and Luspatercept for Myelofibrosis Treatment
This study is testing if combining two medications, momelotinib and luspatercept, can help people with myelofibrosis who need blood transfusions feel better and reduce their transfusion needs.
-
Combining Pacritinib and Talazoparib for Patients with Myeloproliferative Neoplasms Not Responding to JAK2 Therapy
This study is testing a combination of two medications, pacritinib and talazoparib, to see if they can help patients with certain blood cancers who haven't responded to other treatments.
-
Pacritinib and Selinexor in JAK-inhibitor naive myelofibrosis with anemia and low platelets
This trial tests whether combining pacritinib and selinexor helps patients with myelofibrosis who have anemia and low platelets and have not yet tried a JAK inhibitor.
-
National registry for people with myelofibrosis and anemia in Germany.
This project will collect health, treatment, and quality-of-life information from people in Germany with primary or secondary myelofibrosis and anemia to see how their care and symptoms change over time.
-
Evaluating the safety and effectiveness of bomedemstat for blood disorders
This study is trying to see how safe and effective bomedemstat is for people with blood disorders like essential thrombocythemia and myelofibrosis who have been doing well on the treatment for at least six months.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.