Trombositopenisi Olan Miyelofibrozis Hastalarında Kemik İliği Fibrozisi İçin Pacritinib

Sade dilde özet

Bu çalışma, Pacritinib adlı ilacın kemik iliği fibrozisi üzerine etkisini, trombositopenisi (düşük trombosit sayısı) olan miyelofibrozis (myelofibrosis) hastalarında değerlendirmektedir. Çalışmaya, 18 yaş ve üzeri, primer ya da polisitemia vera/esansiyel trombositemi sonrası miyelofibrozis tanısı doğrulanmış ve JAK-2 inhibitörü tedavisine uygun hastalar alınmaktadır. Çalışma Faz 2 aşamasında yürütülmekte olup halen katılımcı almaktadır.

Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.

Deney bilgileri

Faz

Faz 2 (Phase 2)

Durum

Katılımcı alıyor

Sponsor

Grupo Español de Enfermedades Mieloproliferativas Crónicas PH Negativas

Müdahale

Pacritinib

Başlangıç

15.04.2026

Tahmini bitiş

01.06.2028

Ülkeler

Spain

İlgili genler

Merkezler

• Barcelona, Spain
• Barcelona, Spain
• Barcelona, Spain
• Jerez de la Frontera, Spain
• Madrid, Spain
• Madrid, Spain
• Madrid, Spain
• Madrid, Spain
• Murcia, Spain
• Salamanca, Spain
• Valencia, Spain
• Valencia, Spain
• Valencia, Spain

Uygunluk kriterleri

Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.

Inclusion Criteria:

1. Signed written and voluntary informed consent.
2. Age ≥18 years
3. Patients with a confirmed diagnosis of myelofibrosis, either primary myelofibrosis (PMF) or post polycythemia vera (PPV-MF) or post essential thrombocythemia (PET-MF).
4. Patients with thrombocytopenia, delimited by platelets counts between 50 - 120 x 109/L.
5. Patients who require JAK-2 inhibitor therapy in the opinion of the investigator and are eligible to start treatment with pacritinib either in the first line (JAK2 inhibitor-naive) or in second line setting (after no response or loss of response or intolerance to one prior JAK2 inhibitor ).

   Note: patients should have recovered to grade ≤ 1 from any toxicity from previous treatment.
6. Have a Eastern Cooperative Oncology Group Performance Status (ECOG-PS) of 0 - 2.
7. Have a dynamic international prognostic scoring system (DIPSS) Intermediate-1, Intermediate-2, or High risk.
8. Peripheral blasts count \< 5% and absolute neutrophil count (ANC) of ≥500/μL.
9. Adequate liver and renal function, defined by:

   1. liver transaminases, including alanine aminotransferase (ALT or GOT) and aspartate aminotransferase (AST or GOT) ≤ 3 x upper limit normal (ULN). AST/ALT ≤5 × ULN if transaminase elevation is related to MF.
   2. Total bilirubin and/or direct bilirubin ≤ 4 x ULN.
   3. Estimated glomerular filtration rate (eGFR) \> 30 mL/min.
10. Adequate coagulation defined by prothrombin time/international normalized ratio and partial thromboplastin time ≤ 1.5 × ULN.
11. If fertile, willing to use effective birth control methods during the study and up to 30 days after the last dose of pacritinib.
12. Willing to undergo and able to tolerate frequent MRI during the study and BM biopsy
13. Able to understand and willing to complete symptom assessments.

Exclusion Criteria:

1. Life expectancy \<6 months.
2. Splenic irradiation within the last 6 months.
3. Previously treated with pacritinib.
4. Concurrent enrollment in another interventional trial.
5. Treatment with an experimental therapy within 28 days prior to the first dose of study treatment.
6. Systemic treatment with a strong CYP3A4 inhibitor or inducer and the treatment cannot be either discontinued or switched to a different medication within 5 half-lifes prior to study entry.
7. Severe (Child-Pugh C) liver impairment.
8. Significant recent bleeding history defined as NCI CTCAE grade ≥2 within 3 months prior to first dose of study treatment, or with active bleeding, unless precipitated by an inciting event (e.g., surgery, trauma, or injury).
9. Conditions or medications that increase the risk of bleeding, except for aspirin (dosages of ≤100 mg per day). Patients treated with "direct-acting oral anticoagulants (DOACs), could be considered for inclusion (may be consulted with the Sponsor, GEMFIN).
10. Any history of CTCAE grade ≥2 dysrhythmias or non-dysrhythmia cardiac conditions within 6 months prior to the first dose of study treatment. Patients with non-dysrhythmia or non-QTc grade 2 cardiovascular conditions , may be considered for inclusion, if stable , asymptomatic and unlikely to affect patient safety.
11. QT corrected by the Fridericia method (QTcF) prolongation \>480 ms or other factors that increase the risk for QTcF interval prolongation (e.g., heart failure, hypokalemia or history of long QT interval syndrome).
12. New York Heart Association Class II, III, or IV congestive heart failure.
13. Active or uncontrolled inflammatory or chronic functional bowel disorder such as Crohn's disease, inflammatory bowel disease, chronic diarrhea or constipation
14. Other malignancy within 3 years prior to treatment Day 1, other than curatively treated basal cell or squamous cell skin or corneal cancer; curatively treated carcinoma in situ of the cervix. The exception is if patients have been disease-free for at least 5 years, and are deemed by the investigator to be at low risk for recurrence of that malignancy.
15. Known seropositivity for human immunodeficiency virus. Known active hepatitis B, or C virus infection.
16. Women who are pregnant or lactating
17. 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.
18. Any active GI or metabolic condition that could interfere with absorption of oral medication.