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.
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)
- Type of treatment
- Pill or oral medicine, Injection or infusion, Surgery or procedure
- 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
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.
- Conditions
- Sickle Cell Disease, Hemoglobinopathies
- 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 group | Role | What they receive |
|---|---|---|
| Non-Myeloablative Conditioning and Bone Marrow Transplantation | Experimental | Not 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.
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)
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
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
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.
- First posted9 May 2013 (estimated)
- Study startMay 2013
- Primary completionNov 2023
- Study completion31 Dec 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Sickle Cell DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Vanderbilt-Ingram Cancer Center
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Adetola A. Kassim, Vanderbilt-Ingram Cancer Center
- Investigators
- Adetola A Kassim, MD, Principal investigator, Vanderbilt-Ingram Cancer Center
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
- Results posted
- Yes, on ClinicalTrials.gov
- 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 42049986Kassim 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 38493482Aumann 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
Study at a glance
From the registry record, last updated by the sponsor on 10 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT01850108
- Acronym / sponsor ID
- VICCNCCTT12108
- Conditions
- Sickle Cell Disease, Hemoglobinopathies
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 26 participants (actual)
- Lead sponsor
- Vanderbilt-Ingram Cancer CenterUniversity, hospital or other
- Study start
- May 2013 (actual)
- Primary completion
- Nov 2023 (actual)
- Study completion
- 31 Dec 2024 (estimated)
- First posted
- 9 May 2013 (estimated)
- Results
- Posted 10 Jan 2024
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Non-Myeloablative Conditioning and Bone Marrow Transplantation | Experimental | Drug: Thymoglobulin, Drug: Fludarabine, Drug: Cyclophosphamide (CTX), Drug: Mesna, Drug: Sirolimus, Drug: Mycophenolate mofetil (MMF), Procedure: Bone marrow transplantation, Radiation: Total body irradiation |
Who may qualify
- Ages
- 1 year to 70 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ThymoglobulinDay 9 before BMT: 0.5mg/kg IV; Days 8 \& 7 before BMT: 2mg/kg IV Days 8 \& 7 - 2mg/kg IV before BMT | Drug | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
| FludarabineAlso: Fludara®Days 6 and 2 before BMT: 30mg/m2/day IV | Drug | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
| Cyclophosphamide (CTX)Also: CytoxanDays 6 and 5 before BMT: 14.5mg/kg IV; Days 3 and 4 after BMT: 50mg/kg/day | Drug | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
| MesnaDays 3 \& 4 after BMT: 40 mg/kg IV | Drug | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
| SirolimusAlso: 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. | Drug | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
| Mycophenolate mofetil (MMF)15 mg/kg orally with maximum dose 3 mg/day beginning 5 days after BMT and taken to day 35 after BMT | Drug | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
| Bone marrow transplantationDay 0 - Transplantation of hematopoietic cells derived from bone marrow of a donor to a recipient as treatment for hematologic disorders | Procedure or surgery | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
| Total body irradiation200 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 | Radiation | Non-Myeloablative Conditioning and Bone Marrow Transplantation |
Primary outcome
Transplant-related Mortality (TRM)
Time frame: at 1 year after BMT
Defined as death in the absence of recurrent sickle cell disease or hemoglobinopathy
3 secondary outcomes
Number of Patients Who Developed Grade I-IV Acute Graft-vs.-Host Disease
Time frame: 2 years
Number of Patients With Donor Hematopoietic Chimerism in Peripheral Blood <95% at 6 Months After Mini-haploBMT
Time frame: Up to approximately 180 after mini-haploBMT
Number of Participants With Hematologic and Non-hematologic Toxicities Following minihaploBMT
Time frame: Day 60 after BMT
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jan 2024.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 42049986Alasbali 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.
- Derived from this study: PubMed 38493482Kassim 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.
- Derived from this study: PubMed 37883803Aumann 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.
- Vanderbilt-Ingram Cancer Center, Find a Clinical TrialLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Adetola A Kassim, MD principal investigator
Vanderbilt-Ingram Cancer Center
3 sites in 3 countries: see every site and its status.
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.