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Sickle Cell DiseaseNCT01850108

Non-Myeloablative Conditioning and Bone Marrow Transplantation

A study testing Thymoglobulin, Fludarabine and Cyclophosphamide (CTX) in people with Sickle Cell Disease and Hemoglobinopathies, run by Vanderbilt-Ingram Cancer Center at 3 sites in 3 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Allogeneic blood or marrow transplantation (alloBMT) is a curative therapy for a variety of hematologic disorders, including sickle cell disease and thalassemia. Even when it is clear that alloBMT can give to these patients an improvement in their disease, myeloablative transplants have important toxicities and… Read more about this study

Who is it for?
Ages 1 year to 70 yearsHealthy volunteers can take part
Conditions the study is for
Sickle Cell Disease, Hemoglobinopathies
What is being tested?
Thymoglobulin, Fludarabine and Cyclophosphamide (CTX)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
26 participants
Where
3 sitesin 3 countries
Study dates
May 2013to 31 Dec 2024
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 1 year to 70 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

RECIPIENT INCLUSION CRITERIA

  • Patients who are ineligible for BMT from an HLA-matched sibling donor can proceed to a haplo-BMT. Patients with an HLA-matched related donor will proceed to a matched BMT.
  • Age 1-70 years
  • Good performance status (ECOG 0 or 1; Karnofsky and Lansky 70-100)
  • Patients and donors must be able to sign consent forms. First degree relative should be willing to donate
  • Patients must be geographically accessible and willing to participate in all stages of treatment.
  • Eligible diagnoses: Patients with sickle cell anemia such as sickle cell anemia (Hb SS), Hb Sβ° thalassemia, Hb Sβ+thalassemia, Hb SC disease, Hb SE disease, Hb SD disease, Hemoglobin SO- Arab disease HbS with hereditary persistence of fetal hemoglobin. Other significant hemoglobinopathies.

Plus one of the following:

  • Attenuation of progressive disease (adults):
  • Severe and debilitating vaso-occlusive pain despite hydroxyurea or regular blood transfusion therapy.
  • Stroke and silent infarct; stroke or central nervous system event lasting more than 24 hours; MRI changes indicative of brain parenchyma damage and MRA evidence of cerebrovascular disease.
  • Recurrent acute chest syndrome requiring exchange hospitalization.
  • Chronic lung disease as defined by progressive restrictive disease irrespective of oxygen requirements.
  • Chronic kidney disease, CKD stage II - IV
  • Transfusion dépendent thalassemia

RECIPIENT EXCLUSION CRITERIA:

  • Poor performance status (ECOG>1).
  • Poor cardiac function: left ventricular ejection fraction<35%.
  • Poor pulmonary function: FEV1 and FVC<40% predicted.
  • Pulmonary hypertension moderate to severe by echocardiographic standards.
  • Poor liver function: direct bilirubin >3.1 mg/dl
  • HIV-positive
  • Minor (donor anti-recipient) ABO incompatibility if an ABO compatible donor is available.
  • Prior transfusions from donor or recipient if caused alloimmunization vs. donor cells.
  • Women of childbearing potential who currently are pregnant (Beta-HCG+) or who are not practicing adequate contraception.
  • Patients who have any debilitating medical or psychiatric illness that would preclude their giving informed consent or their receiving optimal treatment and follow-up. However, patients with history of stroke and significant cognitive deficit,that would preclude giving informed consent or assent will not be excluded, if they have a family member or significant other with Power of Attorney to also consent of their behalf.

CRITERIA FOR DONOR ELIGIBILITY:

  • Weight ≥ 20kg and age ≥ 18 years or per institutional guidelines
  • Donors must meet the selection criteria as defined by the Foundation for the Accreditation of Hematopoietic Cell Therapy (FAHCT) and will be screened per the American Association of Blood Banks (AABB). (AABB guidelines and the recipients will be informed of any deviations.)
  • HLA-haploidentical first-degree relatives of the patient. Participants must be HLA typed at high resolution using DNA based typing at HLA-A, -B, -C and DRB1 and have available: An HLA haploidentical first degree relative donor (parents, siblings or half siblings, or children) with 2, 3, or 4 (out of 8) HLA-mismatches who is willing and able to donate bone marrow. A unidirectional mismatch in either the graft versus host or host versus graft direction is considered a mismatch. The donor and recipient must be HLA identical for at least one antigen (using high resolution DNA based typing) at the following genetic loci: HLA-A, HLA-B, HLA-C, and HLA-DRB1. Fulfillment of this criterion shall be considered sufficient evidence that the donor and recipient share one HLA haplotype, and typing of additional family members is not required.

When more than one donor is available, the donor with the lowest number of HLA allele mismatches will be chosen, unless there is HLA cross-match incompatibility or a medical reason to select otherwise, in which case donor selection is the responsibility of the PI, in consultation with the immunogenetics laboratory. In cases where there is more than one donor with the least degree of mismatch, donors will be selected based on the most favorable combination of:

  • HLA compatibility in cross-match testing and
  • ABO compatibility
  • Donor age <40 years
  • Avoid female donors for male recipients and
  • Avoid CMV mismatched donor-recipient transplants:

HLA cross-matching (in order of priority):

  • Mutually compatible (no cross-matching antibodies)
  • Recipient non-cross-reactive with donor, donor cross-reactive with recipient
  • Mutually cross-reactive

ABO compatibility (in order of priority):

  • Compatible
  • Major incompatibility
  • Minor incompatibility
  • Major and minor incompatibility
  • Donors will be selected to minimize HLA mismatch in the Host-versus-graft direction.
  • Donors fulfilling the following criteria are ineligible for registration onto this study:
  • All donors will be screened by hemoglobin electrophoresis; donors with a clinically significant hemoglobinopathy are ineligible. Sickle trait is acceptable.

Trial locations and contacts

3 sites in 3 countries.

3 sites in 3 countries

United States1 site
  • Vanderbilt-Ingram Cancer Center

    Nashville, Tennessee, 37232

Other trials in United States

France1 site
  • Saint-Louis Hospital

    Paris

Other trials in France

United Kingdom1 site
  • St Mary's Hospital

    London

Other trials in United Kingdom

About this study

Official title: A Non-Myeloablative Conditioning and Transplantation of Partially HLA-Mismatched and HLA-Matched Bone Marrow for Patients With Sickle Cell Disease and Other Hemoglobinopathies

Allogeneic blood or marrow transplantation (alloBMT) is a curative therapy for a variety of hematologic disorders, including sickle cell disease and thalassemia. Even when it is clear that alloBMT can give to these patients an improvement in their disease, myeloablative transplants have important toxicities and mortalities associated. The lack of suitable donors continues to be a limit to access to transplantation. Substantial progress has been made recently in the development of pre-treatment regimens that facilitate the sustained engraftment of donor marrow with reduced toxicity. Most of these regimens incorporate highly immunosuppressive drugs, which allow the reduction or elimination of myeloablative agents or total body irradiation without endangering the sustained engraftment of HLA-identical allogeneic stem cells. Preliminary results of non-myeloablative allogeneic stem cell transplantation suggest that the procedure can be performed in patients who are ineligible for myeloablative alloBMT, and that sustained remissions of several hematologic malignancies can be obtained.

Being tested
Thymoglobulin, Fludarabine, Cyclophosphamide (CTX), Mesna, Sirolimus
Medical subject headings
Anemia, Sickle Cell, Hemoglobinopathies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ThymoglobulinDrug

    Day 9 before BMT: 0.5mg/kg IV; Days 8 \& 7 before BMT: 2mg/kg IV

    Days 8 \& 7 - 2mg/kg IV before BMT

  • FludarabineDrug

    Also called Fludara®

    Days 6 and 2 before BMT: 30mg/m2/day IV

  • Cyclophosphamide (CTX)Drug

    Also called Cytoxan

    Days 6 and 5 before BMT: 14.5mg/kg IV; Days 3 and 4 after BMT: 50mg/kg/day

  • MesnaDrug

    Days 3 \& 4 after BMT: 40 mg/kg IV

  • SirolimusDrug

    Also called rapamycin, Rapamune®

    Adjusted to maintain a serum trough level of 3-12 ng/mL, taken orally beginning on 5 days after BMT and taken to 1 year after BMT.

  • Mycophenolate mofetil (MMF)Drug

    15 mg/kg orally with maximum dose 3 mg/day beginning 5 days after BMT and taken to day 35 after BMT

  • Bone marrow transplantationProcedure or surgery

    Day 0 - Transplantation of hematopoietic cells derived from bone marrow of a donor to a recipient as treatment for hematologic disorders

  • Total body irradiationRadiation

    200 cGy on the day before BMT. Radiation delivered to the entire body of the recipient to eradicate bone marrow cells in the recipient to prepare the recipient to receive the transplanted

Study groups in NCT01850108
Study groupRoleWhat they receive
Non-Myeloablative Conditioning and Bone Marrow TransplantationExperimentalNot described
Receives: Drug: Thymoglobulin; Drug: Fludarabine; Drug: Cyclophosphamide (CTX); Drug: Mesna; Drug: Sirolimus; Drug: Mycophenolate mofetil (MMF); Procedure: Bone marrow transplantation; Radiation: Total body irradiation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Transplant-related Mortality (TRM)

    Defined as death in the absence of recurrent sickle cell disease or hemoglobinopathy

    Measured: at 1 year after BMT

Secondary outcomes (3)
  1. Number of Patients Who Developed Grade I-IV Acute Graft-vs.-Host Disease

    GVHD Severity was graded using the established National Institutes of Health's consensus criteria [36].

    Measured: 2 years

  2. Number of Patients With Donor Hematopoietic Chimerism in Peripheral Blood <95% at 6 Months After Mini-haploBMT

    Partially human leukocyte antigen (HLA)-mismatched bone marrow from first-degree relatives. Defined in percentages of donor cells in patient's peripheral blood, measured in 4 ways.

    • Mixed donor chimerism: > 0% but < 95%
    • Complete donor chimerism > 95%

    Any amount of donor chimerism after day 60 will be considered as having engrafted

    Measured: Up to approximately 180 after mini-haploBMT

  3. Number of Participants With Hematologic and Non-hematologic Toxicities Following minihaploBMT

    Hematologic toxicity:

    -Absolute neutrophil count (ANC): consecutive values of < 500/µL on 3 different days after chemotherapy post-BMT Platelet count: consecutive values of < 20,000 µL on 3 different days after chemotherapy post-BMT

    Non-hematologic toxicities:

    -Toxicities necessitating hospitalization Toxicities grade 4 or above

    Meets the criteria of the following SAE:

    • Relapse of underlying disease
    • Grade 3 ocular toxicity not related to ocular GVHD
    • Grade 3 related non-hematologic toxicity

    Measured: Day 60 after BMT

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 May 2013 (estimated)
  2. Study startMay 2013
  3. Primary completionNov 2023
  4. Study completion31 Dec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
26 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01850108
Sponsor's protocol ID
VICCNCCTT12108
Status last verified
Jan 2024
First submitted
1 May 2013
Last updated
10 Jan 2024
Data monitoring committee
Yes

Publications

  • Alasbali R, Alzahrani M, Wilkerson K, Akhom P, Alotaibi F, Alahmari B, de la Fuente J, DeBaun MR, Rasheed W, Samarkandi H, El Fakih R, Saleh M, Elhassan T, Alzahrani H, Aljurf M, Almohareb F, Kassim AA, AlAhmari A. Excellent outcomes using a novel reduced intensity conditioning with thiotepa and post-transplant cyclophosphamide for HLA-matched related donor transplant in adolescents and adults with sickle cell disease. Bone Marrow Transplant. 2026 Jul;61(7):847-851. doi: 10.1038/s41409-026-02876-3. Epub 2026 Apr 28.

    PubMed 42049986
  • Kassim AA, de la Fuente J, Nur E, Wilkerson KL, Alahmari AD, Seber A, Bonfim C, Simoes BP, Alzahrani M, Eckrich MJ, Horn B, Hanna R, Dhedin N, Rangarajan HG, Gouveia RV, Almohareb F, Aljurf M, Essa M, Alahmari B, Gatwood K, Connelly JA, Dovern E, Rodeghier M, DeBaun MR. An international learning collaborative phase 2 trial for haploidentical bone marrow transplant in sickle cell disease. Blood. 2024 Jun 20;143(25):2654-2665. doi: 10.1182/blood.2023023301.

    PubMed 38493482
  • Aumann MA, Richerson W, Song AK, Davis LT, Pruthi S, Davis S, Patel NJ, Custer C, Kassim AA, DeBaun MR, Donahue MJ, Jordan LC. Cerebral hemodynamic changes after haploidentical hematopoietic stem cell transplant in adults with sickle cell disease. Blood Adv. 2024 Feb 13;8(3):608-619. doi: 10.1182/bloodadvances.2023010717.

    PubMed 37883803

Questions about this trial

What is this clinical trial studying?

A study testing Thymoglobulin, Fludarabine and Cyclophosphamide (CTX) in people with Sickle Cell Disease and Hemoglobinopathies, run by Vanderbilt-Ingram Cancer Center at 3 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 10 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States, France, United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 10 Jan 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Transplant-related Mortality (TRM) (time frame: at 1 year after BMT). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01850108, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jan 2024.

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Clinical Trial NCT01850108 | AzTrials