Protocol Title: Safety and Feasibility of Autologous CD34+ Hematopoietic Stem Cells Mobilization and Apheresis in Participants With RUNX1 Familial Platelet Disorder

Overview

To evaluate the safety and feasibility of collecting hematopoietic stem cells (HSC) in participants with RUNX1-FPD.

Detailed description

Primary Objective:

\- To evaluate the safety of harvesting HSCs in participants with RUNX1 FPD

Secondary Objective

\- To evaluate the feasibility and other relevant information of collecting HSCs from participants with RUNX1 FPD

Interventions

• Drug G-CSF (filgrastim or biosimilar)
  Given by IV or SC
• Procedure Apheresis
  Given by procedure
• Drug Plerixafor
  Given by IV

Primary outcome measures

• Safety and adverse events (AEs) [Time frame: Through study completion; an average of 1 year.]

Eligibility criteria

Inclusion criteria

Participants who meet all of the following criteria are eligible to be included in the study:

• Are aged ≥ 18 to 75 years

a. Once a favorable review of safety has been completed by the SMC in 3 participants aged ≥ 18 years, the study will be opened to participants aged ≥ 12 years.

• Are willing and able to provide informed consent, as appropriate (either directly or through a legally authorized representative \[LAR\]), as described in Appendix 1, Section 13.1
• Have a confirmed diagnosis of RUNX1 FPD, verified by a Clinical Laboratory Improvement Amendments (CLIA)-certified genetic sequencing report.
• Clearance by apheresis team to proceed
• Have systolic blood pressure ≤ 170 mm Hg and diastolic blood pressure ≤ 95 mmHg
• Are eligible for HSCT per institution requirements
• Have a Lansky (age < 16 years)/Karnofsky performance status of ≥ 70 (see Appendix 2, Section 13.2).
• Are willing and able to comply with protocol-defined contraceptive requirements (see Appendix 3 Section 13.3)
• Have a platelet count ≥ 50,000/μL for initiation of apheresis, assessed within 24 hours prior to the procedure, or, if < 50,000/μL are administered platelets on the day of the collection

a. If the apheresis team decides that a central venous catheter (CVC) is to be placed, platelet count should be ≥ 50,000 prior to catheter placement.

• Have hemoglobin ≥ 7.5 g/dL as assessed within 24 hours prior to the procedure

Exclusion criteria

Participants who meet any of the following criteria are excluded from the study:

• Participants with cognitive impairments and/or any serious unstable pre-existing medical condition or psychiatric disorder that can interfere with safety or with obtaining informed consent or compliance with study procedures.
• Have uncontrolled bleeding
• Are using supplemental oxygen
• Have known severe splenomegaly (≥ 20 cm)
• Have a diagnosis of MDS or hematologic malignancies, as defined by WHO hematolymphoid tumor classification fifth edition (Khourey et al 2022) hematolymphoid tumor classification fifth edition (Khourey et al 2022)
• Have recent prior malignancies except resected basal cell carcinoma or treated cervical carcinoma in situ Note: Cancer treated with curative intent < 5 years previously may be allowed following approval from the study investigator. Cancer treated with curative intent > 5 years previously is allowed.
• Have any prior or current myeloproliferative or a significant coagulation or immunodeficiency disorder
• Have advanced liver disease, defined as any of the following:

• Persistent aspartate transaminase, alanine transaminase, or direct bilirubin value > 5× the upper limit of normal (ULN) at screening
• Screening prothrombin time (PT) or partial thromboplastin time (PTT) > 1.5× ULN
• Have had prior HSCT or gene therapy
• Have history of concomitant sickle cell disease
• Have been treated with an investigational drug within 30 days of screening or 5 half-lives (whichever is longer)
• Have a positive test result for HIV, hepatitis B virus (HBV), or hepatitis C virus (HCV) at screening

• Participants with positive hepatitis B core antibody (HbcAb) and/or hepatitis B-e antibody (HbeAb) are eligible provided viral load is negative by quantitative polymerase chain reaction (qPCR).
• Participants who are positive for anti-hepatitis C antibody are eligible as long as they have a negative HCV viral load by qPCR.
• Have a positive infectious disease panel at screening for human T-lymphotropic virus 1 or 2 (HTLV-1 and HTLV-2), or syphilis (rapid plasma 24 reagin \[RPR\])
• Have clinically significant and active bacterial, viral, fungal, or parasitic infection at screening
• Have a white blood cell (WBC) count < 2 × 109/L
• Have a left ventricular ejection fraction < 45%
• Have a screening estimated glomerular filtration rate < 60 mL/min/1.73 m2
• Have a diagnosis of a significant psychiatric disorder that could seriously impede the ability to participate in the study
• For women of childbearing potential: are pregnant or breastfeeding or lack adequate contraception
• Are unable to comply with the study procedures, as assessed by the investigator

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Basic science

Study locations

United States · 1 center

• MD Anderson Cancer Center — Houston

Identifiers

NCT: NCT06414889 · 2023-0799 · NCI-2024-04300

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗