Acute Myeloid LeukaemiaPhase 2/3COSINCT04217278
A Trial of Treatments to Assess the Effects on Outcome of Adults With AML and MDS Undergoing Allogeneic SCT
A Phase 2/3 study testing Vyxeos, Fludarabine and Busulphan in people with Acute Myeloid Leukaemia and High-risk Myelodysplastic Syndrome, run by University of Birmingham at 14 sites in United Kingdom.
Trial summary
Treatment options for older adults with Acute Myeloid Leukaemia (AML) and Myelodysplasia (MDS) are limited. Although stem cell transplantation remains one of the most effective treatments it is associated with severe side effects which have until recently prevented its use in older adults. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Acute Myeloid Leukaemia, High-risk Myelodysplastic Syndrome
- What is being tested?
- Vyxeos, Fludarabine and Busulphan
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 333 participants
- Where
- 14 sitesUnited Kingdom
- Study dates
- 27 Jan 2020to May 2026
- Phase
- Phase 2/3
- Are there results?
- Not yet: the study is under way
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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Eligibility Criteria for Randomisation 1 (closed to recruitment) Inclusion Criteria for Randomisation 1
- Patients (≥ 18 years old) with a morphological documented diagnosis of AML or MDS who are deemed fit for allo-SCT with one of the following disease characteristics: AML
- Patients in 1st complete remission (CR1) defined as < 5% blasts
- Patients in 2nd complete remission (CR2) defined as < 5% blasts
- Secondary AML (defined as previous history of MDS, antecedent haematological disease or chemotherapy exposure) in CR1 or 2 defined as < 5% blasts MDS
- Patients with advanced or high risk MDS with an IPSS-R of ≥3.5 (intermediate 3.5 or higher) including intermediate or high risk CMML (e.g. CPSS int-2 or high risk)
- Patients with an identified HLA identical sibling or suitable matched unrelated donor (suitable match defined as no greater than a single allele mismatch at HLA-A, -B, -C, DQB1 or DRβ1)
- Patients must be considered suitable/fit to undergo allo-SCT as clinically judged by the Local Investigator
- Females of and male patients of reproductive potential (i.e., not post-menopausal or surgically sterilised) must use appropriate, highly effective, contraception from the point of commencing therapy until 6 months after treatment
- Patients have given written informed consent
- Patients willing and able to comply with scheduled study visits and laboratory tests Exclusion Criteria for Randomisation 1
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- Patients with contraindications to receiving allo-SCT
- Female patients who are pregnant or breastfeeding. All women of childbearing potential must have a negative pregnancy test before commencing treatment
- Adults of reproductive potential not willing to use appropriate, highly effective, contraception during the specified period
- Patients with renal or hepatic impairment as clinically judged by the Local Investigator
- Patients with active infection, HIV-positive or chronic active HBV or HCV.
- Patients with a prior malignancy, except lobular breast carcinoma in situ, fully resected basal cell or squamous cell carcinoma of skin or treated cervical carcinoma in situ, incidental histologic finding of prostate cancer (T1a or T1b using the tumor, node, metastasis (TNM) clinical staging system), previous MDS, CMML, MPN resulting in secondary AML. Cancer treated with curative intent ≥ 5 years previously will be allowed. Cancer treated with curative intent < 5 years previously will not be allowed.
- History of serious hypersensitivity reaction to cytarabine, daunorubicin, or any component of the Vyxeos formulation.
- Known history of Wilson's disease or other copper-related metabolic disorder since copper gluconate is a component of the Vyxeos formulation
Eligibility Criteria for Randomisation 2 Inclusion Criteria for Randomisation 2
- Patients aged between 18 - 54 years with a morphological documented diagnosis of AML or MDS who are deemed fit for a MAC allo-SCT with one of the following disease characteristics: AML o Patients in 1st complete remission (CR1) defined as < 5% blasts
- Patients in 2nd complete remission (CR2) defined as < 5% blasts
- Secondary AML (defined as previous history of MDS, antecedent haematological disease or chemotherapy exposure) in CR1 or 2 defined as < 5% blasts
- Must have received at least two courses of prior intensive chemotherapy prior to transplant unless there are exceptional circumstances. Patients with AML who have achieved CR with Venetoclax based induction regimen treatment as only prior treatment, will also be eligible. MDS
- Patients with advanced or high risk MDS (with an IPSS-R of ≥3.5 (intermediate 3.5 or higher) including intermediate or high risk CMML (e.g. CPSS int-2 or high risk), who have < 10% blasts at the time of randomisation following intensive chemotherapy (including R1 randomisation) or hypomethylating agents if necessary
- Patients with an identified HLA identical sibling or suitable matched unrelated donor (suitable match defined as no greater than a single allele mismatch at HLA-A, -B, -C, DQB1 or DRβ1)
- Patients with an ECOG performance status of 0, 1 or 2
- Patients considered suitable/fit to undergo a MAC allo-SCT as clinically judged by the Local Investigator including:
- Adequate hepatic and renal function as determined by full blood count and biochemistry assessment
- Resolution of any toxic effects of prior therapy (including radiotherapy, chemotherapy or surgical procedures)
- Performance of cardiac or pulmonary function tests (where there is a previous history of cardiac or pulmonary impairment)
- Females of and male patients of reproductive potential (i.e., not post-menopausal or surgically sterilised) must use appropriate, highly effective, contraception from the point of commencing therapy until 12 months after treatment
- Patients have given written informed consent
- Patients willing and able to comply with scheduled study visits and laboratory tests Exclusion Criteria for Randomisation 2
- Patients with contraindications to receiving a MAC allo-SCT 2. Female patients who are pregnant or breastfeeding. All women of childbearing potential must have a negative pregnancy test before commencing treatment 3. Adults of reproductive potential not willing to use appropriate, effective, contraception during the specified period 4. Patients with renal or hepatic impairment as clinically judged by the Local Investigator 5. Patients with active infection, HIV-positive or chronic active HBV or HCV 6. Patients with a prior malignancy, except lobular breast carcinoma in situ, fully resected basal cell or squamous cell carcinoma of skin or treated cervical carcinoma in situ, incidental histologic finding of prostate cancer (T1a or T1b using the tumor, node, metastasis (TNM) clinical staging system), previous MDS, CMML, MPN resulting in secondary AML. Cancer treated with curative intent ≥ 5 years previously will be allowed. Cancer treated with curative intent < 5 years previously will not be allowed.
Eligibility Criteria for Randomisation 3 Inclusion Criteria for Randomisation 3 1. 1. Patients aged between 55 years or older with a morphological documented diagnosis of AML or MDS who are deemed fit for a RIC allo-SCT (or under the age of 55 with comorbidities which are deemed by the local investigator to preclude safe delivery of a MAC allo-SCT may be considered per investigators discretion) with one of the following disease characteristics: AML
- Patients in 1st complete remission (CR1) defined as < 5% blasts
- Patients in 2nd complete remission (CR2) defined as < 5% blasts
- Secondary AML (defined as previous history of MDS, antecedent haematological disease or chemotherapy exposure) in CR1 or 2 defined as < 5% blasts
- Must have received at least two courses of prior intensive chemotherapy prior to transplant unless there are exceptional circumstances. Patients with AML who have achieved CR with Venetoclax based induction regimen treatment, as only prior treatment, will also be eligible.
MDS
- Patients with advanced or high risk MDS (with an IPSS-R of ≥3.5 (intermediate 3.5 or higher) including intermediate or high risk CMML (e.g. CPSS int-2 or high rsk), who have < 10% blasts at the time of randomisation following intensive chemotherapy (including R1 randomisation) or hypomethylating agents if necessary 2. Patients with an identified HLA identical sibling or suitable matched unrelated donor (suitable match defined as no greater than a single allele mismatch at HLA-A, -B, -C, DQB1 or DRβ1) 3. Patients with an ECOG performance status of 0, 1 or 2 4. Patients considered suitable/fit to undergo a RIC allo-SCT as clinically judged by the Local Investigator including: a. Adequate hepatic and renal function as determined by full blood count and biochemistry assessment b. Resolution of any toxic effects of prior therapy (including radiotherapy, chemotherapy or surgical procedures) c. Performance of cardiac or pulmonary function tests (where there is a previous history of cardiac or pulmonary impairment 5. Females of and male patients of reproductive potential (i.e., not post-menopausal or surgically sterilised) must use appropriate, highly effective, contraception from the point of commencing therapy until 12 months after treatment 6. Patients have given written informed consent 7. Patients willing and able to comply with scheduled study visits and laboratory tests Exclusion Criteria for Randomisation 3
- Patients with contraindications to receiving a RIC allo-SCT
- Female patients who are pregnant or breastfeeding. All women of childbearing potential must have a negative pregnancy test before commencing treatment
- Adults of reproductive potential not willing to use appropriate, effective, contraception during the specified period
- Patients with renal or hepatic impairment as clinically judged by the Local Investigator
- Patients with active infection, HIV-positive or chronic active HBV or HCV
- Patients with a prior malignancies, except lobular breast carcinoma in situ, fully resected basal cell or squamous cell carcinoma of skin or treated cervical carcinoma in situ, incidental histologic finding of prostate cancer (T1a or T1b using the tumor, node, metastasis (TNM) clinical staging system), previous MDS, CMML, MPN resulting in secondary AML. Cancer treated with curative intent ≥ 5 years previously will be allowed. Cancer treated with curative intent < 5 years previously will not be allowed.
Trial locations and contacts
14 sites in 1 country.
14 sites in 1 country
United Kingdom14 sites
Queen Elizabeth Hospital
Birmingham
University Hospitals Bristol
Bristol
Addenbrooke's Hospital
Cambridge
University Hospital of Wales
Cardiff
Queen Elizabeth Hospital Glasgow
Glasgow
St James' University Hospital
Leeds
Leicester Royal Infirmary
Leicester
Hammersmith Hospital
London
King's College Hospital
London
Manchester Royal Infirmary
Manchester
Freeman Hospital
Newcastle
Nottingham City Hospital
Nottingham
Churchill Hospital
Oxford
Derriford Hospital
Plymouth
About this study
Official title: An International Randomised Clinical Trial of Therapeutic Interventions to Assess the Effects on Outcome in Adults With Acute Myeloid Leukaemia and High Risk Myelodysplasia Undergoing Allogeneic Stem Cell Transplantation.
Treatment options for older adults with Acute Myeloid Leukaemia (AML) and Myelodysplasia (MDS) are limited. Although stem cell transplantation remains one of the most effective treatments it is associated with severe side effects which have until recently prevented its use in older adults. In the last decade the use of reduced intensity transplants has allowed the extension of the potentially curative effect of transplantation to older patients in whom it was previously precluded. Although a major advance such transplants are associated with a high risk of disease relapse particularly in patients with high risk disease.
This study will evaluate new transplant strategies with the aim of improving the outcome of patients with AML and high risk MDS after stem cell transplantation. Three approaches to improve transplant outcome will be studied:
Read more
- Comparing the new pre-transplant consolidation therapy vyxeos with the standard consolidation therapy (Randomisation 1 is now closed to recruitment).
- Comparing new conditioning therapies in patients under the age of 55 years
- Comparing new conditioning therapies in patients aged 55 and over
All patients will be followed up for a minimum of 2 years.
Read the detailed description
This is a randomised, international, phase II/III, multicentre, clinical trial in patients with AML and MDS undergoing allo-SCT. Patients with AML or MDS who fulfil the eligibility criteria will be invited to participate in the trial across centers performing allo-SCT.
Patients will be randomised to treatment based on a minimisation algorithm prepared at the Cancer Research UK Clinical Trials Unit (CRCTU).
Randomisation 1 (R1) (closed to recruitment) will compare the novel consolidation therapy vyxeos with the standard consolidation therapy intermediate dose cytarabine.
Randomisation 2 (R2) will compare the novel conditioning regimen thiotepa/busulphan/fludarabine (TBF) with the standard conditioning therapy fludarabine/busulphan (FB4) in patients aged under 55 years of age.
Randomisation 3 (R3) will compare the novel conditioning regimen mini thiotepa/busulphan/fludarabine (mini TBF) with the standard regimen fludarabine/busulphan (FB2) in patients aged 55 years of age and over (or patients aged under 55 with comorbidities).
- Being tested
- Vyxeos, Fludarabine, Busulphan, Thiotepa, Cytarabine
- Keywords
- Allogeneic Stem Cell Transplant, AML, MDS
- Medical subject headings
- Leukemia, Myeloid, Acute
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
VyxeosDrug
Also called CPX-351
Vyxeos administered by intravenous infusion
FludarabineDrug
Also called Fludara
Fludarabine administered by intravenous infusion
BusulphanDrug
Also called Busulfan, Bulsivex
Busulphan administered by intravenous infusion
ThiotepaDrug
Also called Tepadina
Thiotepa administered by intravenous infusion
CytarabineDrug
Also called Ara-C, Cytosine arabinoside
Cytarabine administered by intravenous infusion
| Study group | Role | What they receive |
|---|---|---|
| R1: Intermediate dose Cytarabine | Active comparator | First Randomisation (closed to recruitment) - control arm: Intermediate dose Cytarabine (1g/m^2 administered by intravenous infusion over 2 hours on days 1-5 inclusive) Receives: Drug: Cytarabine |
| R1: Vyxeos | Experimental | First Randomisation (closed to recruitment) - experimental arm: Vyxeos (29mg/65mg/m^2 administered by intravenous infusion over 90 minutes on days 1 and 3) Receives: Drug: Vyxeos |
| R2: FB4 | Active comparator | Second Randomisation - under 55 years - control arm: Fludarabine (40mg/m^2 days -7, -6, -5, and -4), Busulphan (3.2mg/kg days -7, -6, -5 and -4) Receives: Drug: Fludarabine; Drug: Busulphan |
| R2: TBF | Experimental | Second Randomisation - under 55 years - experimental arm: Thiotepa (5mg/kg day -7 and -6), Busulphan (3.2mg/kg days -5, -4 and -3), Fludarabine (50mg/m^2 days -5, -4 and -3) Receives: Drug: Fludarabine; Drug: Busulphan; Drug: Thiotepa |
| R3: FB2 | Active comparator | Third Randomisation - 55 years and over (or under 55 with comorbidities) - control arm: Fludarabine (30mg/m^2 days -6, -5, -4, -3 and -2), Busulphan (3.2mg/kg days -6 and -5) Receives: Drug: Fludarabine; Drug: Busulphan |
| Mini-TBF | Experimental | Third Randomisation - 55 years and over (or under 55 with comorbidities) - experimental arm: Thiotepa (5mg/kg day -6), Busulphan (3.2mg/kg days -5 and -4), Fludarabine (50mg/m^2 days -5, -4, and -3) Receives: Drug: Fludarabine; Drug: Busulphan; Drug: Thiotepa |
What is being measured
The primary outcome is the main question the study is designed to answer.
Overall survival (all randomisations)
Defined as time from entering the relevant randomisation to the relevant question until death from any cause. Patients who are alive at the end of the trial or have been lost to follow up will be censored at their date last seen. For randomisations 2 and 3 this outcome will also be calculated as time from transplantation in order to run a sensitivity analysis.
Measured: 12 and 24 months
Secondary outcomes (9)
Change in MRD status - R1 only
Change in minimal residual disease status. A patient will be categorised as either MRD status reduction (MRD positive to negative), MRD remain negative, MRD remain positive or MRD progression (MRD negative to positive) - Randomisation 1 only
Measured: Assessed at baseline and pre-transplant
Disease-free survival
DFS defined as time from randomisation to the relevant question to the first of relapse or death from any cause. Patients who are alive and disease free at the end of the trial will be censored at their date known to be alive.
Measured: From date of randomisation through to study completion, an average of 6 years
Cumulative incidence of disease relapse
CIR defined as time from randomisation to the relevant question to the date of relapse. Patients who die prior to relapse will be treated as a competing risk and patients who are alive and relapse free at the end of the trial will be censored at their date last seen.
Measured: From date of randomisation through to study completion, an average of 6 years
Non-relapse mortality
NRM defined as the time from randomisation to the relevant question to date of non-relapse death. Patients who die post-relapse will be treated as a competing risk and patients who are alive at the end of the trial will be censored at their date last seen.
Measured: From date of randomisation through to study completion, an average of 6 years
Quality of Life measured by EORTC-QLQ-C30 questionnaires, recorded at multiple timepoints - R2 and R3 only
The EORTC QLQ-C30 uses for the questions 1 to 28 a 4-point scale. The scale scores from 1 to 4 ("Not at all" to "Very much"). For the raw score, less points are considered to have a better outcome. For the questions 29 and 30 it uses a 7-points scale. The scale scores from 1 to 7 ("very poor" to "excellent"). More points are considered to have a better outcome.
Measured: Assessed at pre transplant, day 28 and months 3, 6, 9, 12, 18 and 24
Quality of Life measured by EQ-5D questionnaires, recorded at multiple timepoints - R2 and R3 only
EQ5D is one of the most widely used health states descriptive system. EQ-5D questionnaires have 5 dimensions: "Mobility", "Human Autonomy," "Current Activities", "Pain / Discomfort", "Anxiety / Depression" and all dimensions are described by 3 problem levels corresponding to patient response choices. A quality of life score is obtained according to the answers to the questionnaires.
Measured: Assessed at pre transplant, day 28 and months 3, 6, 9, 12, 18 and 24
Incidence of acute and chronic Graft versus Host Disease - R2 and R3 only
Incidence of acute and chronic GvHD of any grade - Randomisation 2 and 3 only
Measured: From date of randomisation through to study completion, an average of 6 years
Incidence of primary graft failure - R2 and R3 only
Defined as loss of donor cells after transplantation - Randomisation 2 and 3 only
Measured: From date of randomisation through to study completion, an average of 6 years
Incidence of toxicities reported as per CTCAE V4.0
Defined as the number of patients who report one or more adverse event of grade 3 or higher or a serious adverse event of any grade
Measured: From start of treatment until 28 days after last dose of treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Jan 2020
- Study start27 Jan 2020
- Primary completionMay 2026 (estimated)
- Study completionMay 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Acute Myeloid LeukaemiaStudies 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 2/3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 333 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Birmingham
- Sponsor type
- University, hospital or other
- Collaborators
- Jazz Pharmaceuticals, Adienne SA
- Responsible party
- Sponsor
- Investigators
- Charles Craddock, Professor, Principal investigator, University Hospital Birmingham NHS Foundation Trust
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04217278
- Sponsor's protocol ID
- RG_17-234
- Acronym
- COSI
- Status last verified
- Apr 2026
- First submitted
- 20 Nov 2019
- Last updated
- 5 May 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An International Randomised Clinical Trial of Therapeutic Interventions to Assess the Effects on Outcome in Adults With Acute Myeloid Leukaemia and High Risk Myelodysplasia Undergoing Allogeneic Stem Cell Transplantation.
- ClinicalTrials.gov ID
- NCT04217278
- Acronym / sponsor ID
- COSI / RG_17-234
- Keywords
- Allogeneic Stem Cell Transplant, AML, MDS
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 333 participants (actual)
- Lead sponsor
- University of BirminghamUniversity, hospital or other
- Collaborators
- Jazz Pharmaceuticals, Adienne SA
- Study start
- 27 Jan 2020 (actual)
- Primary completion
- May 2026 (estimated)
- Study completion
- May 2026 (estimated)
- First posted
- 3 Jan 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Treatment options for older adults with Acute Myeloid Leukaemia (AML) and Myelodysplasia (MDS) are limited. Although stem cell transplantation remains one of the most effective treatments it is associated with severe side effects which have until recently prevented its use in older adults. In the last decade the use of reduced intensity transplants has allowed the extension of the potentially curative effect of transplantation to older patients in whom it was previously precluded. Although a major advance such transplants are associated with a high risk of disease relapse particularly in patients with high risk disease.
This study will evaluate new transplant strategies with the aim of improving the outcome of patients with AML and high risk MDS after stem cell transplantation. Three approaches to improve transplant outcome will be studied:
- Comparing the new pre-transplant consolidation therapy vyxeos with the standard consolidation therapy (Randomisation 1 is now closed to recruitment).
- Comparing new conditioning therapies in patients under the age of 55 years
- Comparing new conditioning therapies in patients aged 55 and over
All patients will be followed up for a minimum of 2 years.
Detailed description
This is a randomised, international, phase II/III, multicentre, clinical trial in patients with AML and MDS undergoing allo-SCT. Patients with AML or MDS who fulfil the eligibility criteria will be invited to participate in the trial across centers performing allo-SCT.
Patients will be randomised to treatment based on a minimisation algorithm prepared at the Cancer Research UK Clinical Trials Unit (CRCTU).
Randomisation 1 (R1) (closed to recruitment) will compare the novel consolidation therapy vyxeos with the standard consolidation therapy intermediate dose cytarabine.
Randomisation 2 (R2) will compare the novel conditioning regimen thiotepa/busulphan/fludarabine (TBF) with the standard conditioning therapy fludarabine/busulphan (FB4) in patients aged under 55 years of age.
Randomisation 3 (R3) will compare the novel conditioning regimen mini thiotepa/busulphan/fludarabine (mini TBF) with the standard regimen fludarabine/busulphan (FB2) in patients aged 55 years of age and over (or patients aged under 55 with comorbidities).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 6
| Arm | Type | Receives |
|---|---|---|
| R1: Intermediate dose Cytarabine | Active comparator | Drug: CytarabineFirst Randomisation (closed to recruitment) - control arm: Intermediate dose Cytarabine (1g/m^2 administered by intravenous infusion over 2 hours on days 1-5 inclusive) |
| R1: Vyxeos | Experimental | Drug: VyxeosFirst Randomisation (closed to recruitment) - experimental arm: Vyxeos (29mg/65mg/m^2 administered by intravenous infusion over 90 minutes on days 1 and 3) |
| R2: FB4 | Active comparator | Drug: Fludarabine, Drug: BusulphanSecond Randomisation - under 55 years - control arm: Fludarabine (40mg/m^2 days -7, -6, -5, and -4), Busulphan (3.2mg/kg days -7, -6, -5 and -4) |
| R2: TBF | Experimental | Drug: Fludarabine, Drug: Busulphan, Drug: ThiotepaSecond Randomisation - under 55 years - experimental arm: Thiotepa (5mg/kg day -7 and -6), Busulphan (3.2mg/kg days -5, -4 and -3), Fludarabine (50mg/m^2 days -5, -4 and -3) |
| R3: FB2 | Active comparator | Drug: Fludarabine, Drug: BusulphanThird Randomisation - 55 years and over (or under 55 with comorbidities) - control arm: Fludarabine (30mg/m^2 days -6, -5, -4, -3 and -2), Busulphan (3.2mg/kg days -6 and -5) |
| Mini-TBF | Experimental | Drug: Fludarabine, Drug: Busulphan, Drug: ThiotepaThird Randomisation - 55 years and over (or under 55 with comorbidities) - experimental arm: Thiotepa (5mg/kg day -6), Busulphan (3.2mg/kg days -5 and -4), Fludarabine (50mg/m^2 days -5, -4, and -3) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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 |
|---|---|---|
| VyxeosAlso: CPX-351Vyxeos administered by intravenous infusion | Drug | R1: Vyxeos |
| FludarabineAlso: FludaraFludarabine administered by intravenous infusion | Drug | Mini-TBF, R2: FB4, R2: TBF, R3: FB2 |
| BusulphanAlso: Busulfan, BulsivexBusulphan administered by intravenous infusion | Drug | Mini-TBF, R2: FB4, R2: TBF, R3: FB2 |
| ThiotepaAlso: TepadinaThiotepa administered by intravenous infusion | Drug | Mini-TBF, R2: TBF |
| CytarabineAlso: Ara-C, Cytosine arabinosideCytarabine administered by intravenous infusion | Drug | R1: Intermediate dose Cytarabine |
Primary outcome
Overall survival (all randomisations)
Time frame: 12 and 24 months
Defined as time from entering the relevant randomisation to the relevant question until death from any cause. Patients who are alive at the end of the trial or have been lost to follow up will be censored at their date last seen. For randomisations 2 and 3 this outcome will also be calculated as time from transplantation in order to run a sensitivity analysis.
9 secondary outcomes
Change in MRD status - R1 only
Time frame: Assessed at baseline and pre-transplant
Disease-free survival
Time frame: From date of randomisation through to study completion, an average of 6 years
Cumulative incidence of disease relapse
Time frame: From date of randomisation through to study completion, an average of 6 years
Non-relapse mortality
Time frame: From date of randomisation through to study completion, an average of 6 years
Quality of Life measured by EORTC-QLQ-C30 questionnaires, recorded at multiple timepoints - R2 and R3 only
Time frame: Assessed at pre transplant, day 28 and months 3, 6, 9, 12, 18 and 24
Quality of Life measured by EQ-5D questionnaires, recorded at multiple timepoints - R2 and R3 only
Time frame: Assessed at pre transplant, day 28 and months 3, 6, 9, 12, 18 and 24
Incidence of acute and chronic Graft versus Host Disease - R2 and R3 only
Time frame: From date of randomisation through to study completion, an average of 6 years
Incidence of primary graft failure - R2 and R3 only
Time frame: From date of randomisation through to study completion, an average of 6 years
Incidence of toxicities reported as per CTCAE V4.0
Time frame: From start of treatment until 28 days after last dose of treatment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 May 2026.
- Individual participant dataSharing planned: No
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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.
Charles Craddock, Professor principal investigator
University Hospital Birmingham NHS Foundation Trust
14 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2/3 study testing Vyxeos, Fludarabine and Busulphan in people with Acute Myeloid Leukaemia and High-risk Myelodysplastic Syndrome, run by University of Birmingham at 14 sites in United Kingdom.
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: under way, not looking for participants, as of the sponsor's last update on 5 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 14 sites in 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.
What does this combined phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
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?
Overall survival (all randomisations) (time frame: 12 and 24 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 5 May 2026.