High Dose Ruxolitinib and Allogeneic Stem Cell Transplantation in Myelofibrosis Patients With Splenomegaly

Myelofibrosis Clinical Trial

Official title:

High Dose Ruxolitinib and Allogeneic Stem Cell Transplantation in Myelofibrosis Patients With Splenomegaly

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06345495
• Other study ID #: 2023-0899
• Secondary ID: NCI-2024-02814
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: September 30, 2024
• Est. completion date: January 1, 2029

Study information

• Verified date: May 2024
• Source: M.D. Anderson Cancer Center
• Contact: Uday Popat, MD
• Phone: (713) 563-0812
• Email: upopat[@]mdanderson.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To learn if giving ruxolitinib and busulfan before a stem cell transplant can help to reduce spleen size and help the transplant to succeed.

Description:

Primary Objective 1) Compare the proportion of patients alive, disease free, engrafted, and without poor graft function at 100 days post-transplant with the historical rate of 45%. Secondary Objectives: 1. Overall survival 2. Progression-free survival 3. Graft vs host disease relapse free survival 4. Relapse rate 5. Non-relapse Mortality 6. Time to Neutrophil and platelet engraftment 7. Time to red cell transfusion independence 8. Graft failure 9. Acute and chronic GVHD 10. Grade 3 -5 Toxicity 11. Incidence of poor graft function5 12. Need for growth factors (myeloid or thrombopoietic) at 100 days 13. Spleen response around day -7, -1, 30, and 100 days 14. Need for transfusions at 100 days 15. Time to discontinuation of immunosuppressives Exploratory Objectives: 1. Immune reconstitution 2. Cytokine profile

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: January 1, 2029
• Est. primary completion date: January 1, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Participants 18 years to less than or equal to 75 years.

2. Able to provide written consent.

3. Primary or secondary Myelofibrosis (may have received Jak inhibitors including ruxolitinib)

4. Enlarged spleen by palpation or imaging. For the purpose of this study, splenomegaly is defined as any clinically palpable spleen or spleen larger than 12 cms on imaging.

5. Has a fully matched (8/8:HLA A, B, C, DRB1) related or matched unrelated donor.

6. Adequate renal function, including:

a. Serum creatinine </= 1.5 mg/dL or estimated Glomerular Filtration Rate (eGFR using the CKI-EPI equation) >/= 40 ml/min/1.73 m2.

7. Adequate liver function, including:

1. ALT/AST </= 3 x ULN

2. Direct bilirubin </= 1mg/dL

3. No history of liver cirrhosis. No ascites.

8. Female participants of childbearing potential must have negative results for a serum pregnancy test. Female participants must agree to not breastfeed during the study and for 3 months post-completion of the study therapy.

9. Subjects who are of childbearing potential, sexually active, and at risk of pregnancy must agree to use a highly effective method of contraception for the duration of the active treatment and at least 3 months post-completion of the study therapy. Highly

effective methods of contraception include the following:

1. Hormonal contraception (i.e., birth control pills, injection, implant, transdermal patch, vaginal ring), Intrauterine device (IUD), Tubal Ligation or hysterectomy, Subject/Partner post vasectomy, Implantable or injectable contraceptives, and condoms plus spermicide. Not engaging in sexual activity for the total duration of the trial and the drug washout period is an acceptable practice; however periodic abstinence, the rhythm method, and the withdrawal method are not acceptable methods of birth control. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.

2. Men treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of study participation, and 4 months after completion of study agent administration. Men who are able to have children must use effective birth control while on the study. If the male participant fathers a child or suspects that he has fathered a child while on the study, he must immediately notify his doctor.

Exclusion Criteria:

1. Positive beta HCG in females of child-bearing potential defined as not postmenopausal for 24 months or no previous surgical sterilization or lactating females.

2. Ejection fraction <40%

3. Corrected DLCO < 50%

4. Evidence of other clinically significant uncontrolled condition(s) including, but not

limited to:

1. Uncontrolled and/or active systemic infection (viral, bacterial or fungal)

2. Prior hepatitis B virus (HBV), hepatitis C (HCV), HIV or TB infection or requiring treatment for the same.

3. Thrombosis including MI, Stroke, PE, DVT in the past 6 months Note: subjects with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface (HBs) antigen negative-, anti-HBs antibody positive and anti-hepatitis B core (HBc) antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate.

Related Conditions & MeSH terms

• Myelofibrosis
• Primary Myelofibrosis
• Splenomegaly

Intervention

Drug:
• Ruxolitinib
Given by PO

Procedure:
• Allogeneic Stem Cell Transplantation
Given by Transplant

Drug:
• Levetiracetam
Given by PO
• Eltrombopag
Given by PO
• Busulfan
Given by IV
• Romiplostim
Given by IV
• Fludarabine phosphate
Given by IV
• Cyclophosphamide
Given by IV
• Mesna
Given by IV
• Tacrolimus
Given by IV or PO

Locations

Country	Name	City	State
United States	MD Anderson Cancer Center	Houston	Texas

Sponsors (2)

Lead Sponsor	Collaborator
M.D. Anderson Cancer Center	Incyte Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and adverse events (AEs)	Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0	Through study completion; an average of 1 year.

External Links

•   MD Anderson Cancer Center