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NCT Number: NCT03121001

Study of HLA-Haploidentical Stem Cell Transplantation to Treat Clinically Aggressive Sickle Cell Disease

The study is a Phase II clinical trial. Patients will receive intensity modulated total body irradiation (TBI) at a dose of 3 Gy with standard fludarabine/ i.v. cyclophosphamide conditioning prior to human leukocyte antigen (HLA)-haploidentical hematopoietic stem cell transplant (HSCT).

The primary objective of the study is to determine the engraftment at Day +60 following HLA-haploidentical hematopoietic stem cell transplant protocol using immunosuppressive agents and low-dose total body irradiation (TBI) for conditioning and post-transplant cyclophosphamide in patients with sickle cell disease.

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Key information

Age range

16 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Illinois at Chicago

Chicago, Illinois, 60612, United States

Location status: Recruiting

Location contact

Damiano Rondelli, MD

CONTACT

[email protected]

312-413-3547

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Patient Eligibility:

  • Patients with sickle cell disease are eligible if they have any of the following complications:

1.1 Stroke or central nervous system event lasting longer than 24 hours 1.2 Frequent vaso-occlusive pain episodes, defined as ≥ 3 per year requiring emergency room, acute care center, hospital admissions, or home bedrest leading to absence from work or school. 1.3 Recurrent episodes of priapism, defined as ≥ 2 per year requiring emergency room visits 1.4 Acute chest syndrome with recurrent hospitalizations, defined as ≥ 2 lifetime events 1.5 Red-cell alloimmunization (≥ 2 antibodies) during long-term transfusion therapy 1.6 Bilateral proliferative retinopathy with major visual impairment in at least one eye 1.7 Osteonecrosis of 2 or more joints 1.8 Sickle cell nephropathy, defined by a GFR < 90mL/min/1.73m2 or the presence of macroalbuminuria (urine albumin > 300 mg/g creatinine) 1.9 Pulmonary hypertension, defined by a mean pulmonary arterypressure >25mmHg

  • Age 16-60 years
  • Karnofsky performance status of 60 or higher (Appendix A)
  • Adequate cardiac function, defined as left ventricular ejection fraction ≥ 40%
  • Adequate pulmonary function, defined as diffusion lung capacity of carbon monoxide ≥ 50% predicted (after adjustment for hemoglobin concentration)
  • Estimated GFR ≥ 50mL/min/1.73m2 as calculated by the modified MDRD equation
  • ALT ≤ 3x upper limit of normal
  • HIV-negative
  • Patient is not pregnant
  • Patient is able and willing to sign informed consent
  • Patient does not have a fully HLA-matched sibling donor
  • Patient has an HLA-haploidentical relative

Donor Eligibility Relatives (parents, offspring, siblings, aunts/uncles, cousins) will be tested by molecular typing of HLA class I (A, B, and C) and class II (DRB1) at low resolution. Only those that are an HLA-haploidentical match (≥ 4/8) will be considered as a potential donor. NOTE: If during testing, a fully HLA-matched sibling donor is found and is willing to donate his/her stem cells, the potential subject will not be eligible for this protocol.

Donor consent will be obtained as per standard protocol of the bone marrow transplant unit.

Treatment and study plan

ATG

Drug

0.5 mg/kg IV on day -9, and 2 mg/kg on days -8 and day -7

Other names: Thymoglobulin®

Fludarabine

Drug

30 mg/m2 IVPB daily for day -6 (6 days before stem cell infusion) through day -2

Cyclophosphamide

Drug

14.5 mg/kg IV on days -6 and -5 and 50 mg/kg/d on days +3 and +4

Total Body Irradiation

Radiation

3 Gy on day -1

Stem Cell Infusion

Procedure

Stem cell product infused according to BMT unit policy on day 0.

sirolimus

Drug

loading dose of 15 mg followed by 5 mg per day on day +5

Mycophenolate mofetil

Drug

1 g every 8 h (until day 35) will be started on day 5

Primary outcomes

  1. Estimate the number of patients who engraft by Day +60

    Time frame: Up to Day +60

    Patients who achieve < 5% peripheral blood donor chimerism by Day +30 and do not have a Day +60 measure will be regarded as failing to achieve full donor chimerism by Day +60; patients who achieve > 5% donor chimerism by Day +30 but do not have a Day +60 measure will be considered nonevaluable for the primary endpoint.

Secondary outcomes

  1. Disease free survival

    Time frame: Up to Day +60

    Using the Kaplan-Meier method, the probability of EFS will be estimated and reported with 90% confidence intervals. The proportion of patients who are alive will also be estimated with a 90% exact binomial confidence interval. Cumulative incidences of transplant related mortality will be estimated separately using Grey's method.

  2. Overall survival

    Time frame: Up to Day +60

    Using the Kaplan-Meier method, the probability of overall survival will be estimated and reported with 90% confidence intervals. The proportion of patients who are alive will also be estimated with a 90% exact binomial confidence interval. Cumulative incidences of transplant related mortality will be estimated separately using Grey's method.

  3. Adverse Effects

    Time frame: Up to Day +60

    The cumulative incidence of acute (grade II-IV, grade III-IV) and chronic GVHD will be estimated through competing-risk analysis using Grey's method, wherein graft failure, and death are competing risks for GVHD. Other selected toxicities (including rates of infection) will be reported descriptively.

Study contacts

Contact information is provided by the study sponsor or research team.

Damiano Rondelli, MD

CONTACT

[email protected]

312 413-3547

Sponsors and collaborators

Lead sponsor

University of Illinois at Chicago

Other

Registry information

Official study title

A Phase II Study of HLA-Haploidentical Stem Cell Transplantation to Treat Clinically Aggressive Sickle Cell Disease

Important dates

Study start
2017
Primary completion
2029
Study completion
2029
First posted
Apr 19, 2017
Registry last updated
Jul 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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