Hematologic NeoplasmsPhase 3HAPLOMUDNCT02623309
Studyof Allogeneic Hematopoietic Stem Cell Transplantation From One Haplotype Mismatch Related Donor or From an Unrelated Donor in Elderly Patients
A Phase 3 study testing Allogeneic (Allo) hematopoietic stem cell transplantation in people with Hematologic Neoplasms, run by Institut Paoli-Calmettes at 14 sites in France.
Trial summary
Allogeneic (Allo) hematopoietic stem cell transplantation (HSCT) is a recognized curative procedure for hematological malignancies. It is now well known that this property is related to the graft-versus-tumor (GVT) effect developed from the immunocompetent cells contained in or generating from the donor graft. Read more about this study
- Who is it for?
- Ages 55 to 70 years
- Conditions the study is for
- Hematologic Neoplasms
- What is being tested?
- Allogeneic (Allo) hematopoietic stem cell transplantation
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 108 participants
- Where
- 14 sitesFrance
- Study dates
- 23 Feb 2016to 12 Mar 2021
- Phase
- Phase 3
- Are there results?
- None posted in the registry
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 55 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients aged of 55 years or up to 70 years.
- Patients with hematological malignancy
- Patients without a matched related donor
- Patients eligible for an allogeneic HSCT from an alternative donor
- Able to comply with the protocol
- Written informed consent
- Affiliation to Social Security System
Who cannot join
- Clinical or biological contraindication to allogeneic HSCT
- Other evolutive cancer
- Positive serology for HIV, hepatitis B or chronic active hepatitis C
- Pregnant or breast-feeding women.
- Emergency
- Patient considered socially or psychologically unable to comply with the treatment and the required medical follow-up.
Trial locations and contacts
14 sites in 1 country.
14 sites in 1 country
France14 sites
CHU Amiens
Amiens
CHU Besançon
Besançon
CHU Estaing/Clermont-ferrand
Clermont-Ferrand
CHU Albert Michallon
Grenoble
CHU Limoges
Limoges
Institut Paoli Calmettes
Marseille, 13009
CHRU Montpellier
Montpellier
CHU Nantes
Nantes
Hôpital Necker
Paris
Hôpital Saint Antoine
Paris
Hôpital Saint Louis
Paris
Hôpital Haut Leveque
Pessac
Institut de Cancérologie Lucien Neuwirth
Saint-Priest-en-Jarez
IUCT
Toulouse
About this study
Allogeneic (Allo) hematopoietic stem cell transplantation (HSCT) is a recognized curative procedure for hematological malignancies. It is now well known that this property is related to the graft-versus-tumor (GVT) effect developed from the immunocompetent cells contained in or generating from the donor graft. For years, however, and despite this unique antitumoral activity, Allo-HSCT has been restricted to a limited number of patients due to two major limitations: the toxicity of the procedure and the absence of a donor for every single patients. More recently the stage has dramatically changed with respect to these two restraints. Over the last decade, many studies have established the feasibility of Allo-HSCT in older patients but the availability of MRD is even less frequent in elderlies, likely related to medical contraindication for graft donation or sibling deaths. UD are routinely used but associated with a high incidence of GVHD. As compared to younger populations, unrelated cord-blood HSCT is seldom performed in this population and numbers decrease with age due to the feared risk of supposed increased lethal infectious complications related to the effect of the delayed immune reconstitution in elderlies. Thus the need for alternative donors allowing for a safe and efficient transplantation is still unmet. In consequence, overall, despite the fact that Allo-HSCT feasibility has been established in the oldest patients, all these lacks contribute eventually to maintain a low rate of allo-HSCT performed in a population with the higher incidence of hematologic malignancies that usually present with the poorest prognosis.
Thus it is critical developing innovative efficient therapeutic strategies answering this unmet-medical need. In this perspective, Haplo-HSCT could represent a part of the answer in this aged population. It offers the potential advantage to offer a rapid donor determination for virtually every single patient. In addition, our data suggest that in elderlies haplo-HSCT using T-repleted graft, RIC and PT-HDCy presents low NRM and retains an antitumor effect despite low GVHD incidences. They also suggest that haplo-HSCT may conduct to better outcome than URD-HSCT as an alternative to MRD-HSCT. It may also be associated with lower costs (no graft purchase and low post-transplant complications rate) and better QOL likely related to low cGVHD-rate. In addition the conduct of such trial at a time when the diffusion of the strategy in this population is just starting is really crucial before widespread uncontrolled dissemination.
Read more
The investigators propose to address this question by prospectively comparing these 2 strategies in elderly patients without MRD, in terms of efficacy, safety and including the prospective evaluation study of quality-of-life (QOL). They will conduct a national, multicenter, open-label, comparative, randomized phase III trial in patients with hematological malignancies justifying an allo-HSCT from an alternative donor when a MRD has not been identified.
When MRD search is recognized to be a failure, patients will be included in the clinical trial after informed consent and randomized in the two strategies based on donor search:
- Reference group: Unrelated Donor group
- Investigational group: Haplo Donor Group
Investigators will use a composite end-point embracing the three main causes of failure: death, relapse and severe cGVHD (as a surrogate endpoint for QOL). We will analyze the HSCT usual objectives as GHVD, NRM, relapse and survival. A specific study of patients' health related quality of life will also be conducted using the FACT-BMT questionnaire. In addition, the success of the two strategies in term of transplant completion (donor determination, transplant realization and time to do so) will be compared.
- Conditions
- Hematologic Neoplasms
- Being tested
- Allogeneic (Allo) hematopoietic stem cell transplantation
- Medical subject headings
- Hematologic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Allogeneic (Allo) hematopoietic stem cell transplantationBiological
| Study group | Role | What they receive |
|---|---|---|
| HAPLO graft | Experimental | Conditioning regimen
* Fludarabin : 30 mg/m2/day for 4 days: from D-5 à J-2.
* Busulfan IV : 130 mg/m2/day for 2 days : drom D-4 to D-3. + 1 day of Thiotepa : 5mg/kg at D-6.
Prophylaxis regimen for GVHD
* F CSA and MMF (starting day +5)
* Additional immunosuppression: PT-HDCy (50 mg/kg/day) on days +3 and +4
Hematopoietic Stem Cell Graft PBSC graft will be preferred for a minimal targeted cell dose of 4 x 106 CD34+cells/kg GCSF (Neupogen ®) during 4 to 5 days (D-4 to D-1): SC 10 µg/kg/d. Receives: Biological: Allogeneic (Allo) hematopoietic stem cell transplantation |
| MUD graft | Active comparator | Conditioning regimen
* Fludarabin : 30 mg/m2/day for 5 days: from D-6 to D-2.
* Busulfan IV : 130 mg/m2/day for 2 days: from D-4 to D-3.
Prophylaxis regimen for GVHD
* CSA and MMF will be used from day -1 after UD
* Additional immunosuppression: Rabbit ATG (2.5 mg/kg/day) on days -3 and -2
Hematopoietic Stem Cell Graft PBSC graft will be preferred for a minimal targeted cell dose of 4 x 106 CD34+cells/kg Receives: Biological: Allogeneic (Allo) hematopoietic stem cell transplantation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Event-free survival with death, relapse or occurrence of severe cGVHD as event whatever occurs first
Measured: 5 years
Secondary outcomes (7)
Engraftment: time to reach 0.5 x 109/l ANC, 20 x 109/l platelets and full donor lymphoid chimerism
Measured: 5 years
Acute and chronic GVHD cumulative incidences
Measured: 5 years
Non-relapse mortality cumulative incidence
Measured: 5 years
Relapse incidence
Measured: 5 years
Probabilities of overall survival and progression-free survival
Measured: 5 years
Evaluation of HRQL including patients who relapse
Measured: 5 years
Evaluation of procedure costs from beginning of search until death or two-year follow-up
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Dec 2015 (estimated)
- Study start23 Feb 2016
- Primary completion2 Feb 2021
- Study completion12 Mar 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hematologic NeoplasmsStudies of the same condition, open and under way.
- More trials run by Institut Paoli-CalmettesThe sponsor's other registered studies.
- 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 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 108 participants (actual)
Sponsor and investigators
- Lead sponsor
- Institut Paoli-Calmettes
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Didier Blaise, MD, Principal investigator, Institut Paoli-Calmettes
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02623309
- Sponsor's protocol ID
- HAPLOMUDELDERLY-IPC 2015-004
- Acronym
- HAPLOMUD
- Status last verified
- Oct 2026
- First submitted
- 30 Nov 2015
- Last updated
- 16 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 16 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Studyof Allogeneic Hematopoietic Stem Cell Transplantation From One Haplotype Mismatch Related Donor or From an Unrelated Donor in Elderly Patients
- ClinicalTrials.gov ID
- NCT02623309
- Acronym / sponsor ID
- HAPLOMUD / HAPLOMUDELDERLY-IPC 2015-004
- Conditions
- Hematologic Neoplasms
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 108 participants (actual)
- Lead sponsor
- Institut Paoli-CalmettesUniversity, hospital or other
- Study start
- 23 Feb 2016 (actual)
- Primary completion
- 2 Feb 2021 (actual)
- Study completion
- 12 Mar 2021 (actual)
- First posted
- 7 Dec 2015 (estimated)
- 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.
Allogeneic (Allo) hematopoietic stem cell transplantation (HSCT) is a recognized curative procedure for hematological malignancies. It is now well known that this property is related to the graft-versus-tumor (GVT) effect developed from the immunocompetent cells contained in or generating from the donor graft. For years, however, and despite this unique antitumoral activity, Allo-HSCT has been restricted to a limited number of patients due to two major limitations: the toxicity of the procedure and the absence of a donor for every single patients. More recently the stage has dramatically changed with respect to these two restraints. Over the last decade, many studies have established the feasibility of Allo-HSCT in older patients but the availability of MRD is even less frequent in elderlies, likely related to medical contraindication for graft donation or sibling deaths. UD are routinely used but associated with a high incidence of GVHD. As compared to younger populations, unrelated cord-blood HSCT is seldom performed in this population and numbers decrease with age due to the feared risk of supposed increased lethal infectious complications related to the effect of the delayed immune reconstitution in elderlies. Thus the need for alternative donors allowing for a safe and efficient transplantation is still unmet. In consequence, overall, despite the fact that Allo-HSCT feasibility has been established in the oldest patients, all these lacks contribute eventually to maintain a low rate of allo-HSCT performed in a population with the higher incidence of hematologic malignancies that usually present with the poorest prognosis.
Thus it is critical developing innovative efficient therapeutic strategies answering this unmet-medical need. In this perspective, Haplo-HSCT could represent a part of the answer in this aged population. It offers the potential advantage to offer a rapid donor determination for virtually every single patient. In addition, our data suggest that in elderlies haplo-HSCT using T-repleted graft, RIC and PT-HDCy presents low NRM and retains an antitumor effect despite low GVHD incidences. They also suggest that haplo-HSCT may conduct to better outcome than URD-HSCT as an alternative to MRD-HSCT. It may also be associated with lower costs (no graft purchase and low post-transplant complications rate) and better QOL likely related to low cGVHD-rate. In addition the conduct of such trial at a time when the diffusion of the strategy in this population is just starting is really crucial before widespread uncontrolled dissemination.
The investigators propose to address this question by prospectively comparing these 2 strategies in elderly patients without MRD, in terms of efficacy, safety and including the prospective evaluation study of quality-of-life (QOL). They will conduct a national, multicenter, open-label, comparative, randomized phase III trial in patients with hematological malignancies justifying an allo-HSCT from an alternative donor when a MRD has not been identified.
When MRD search is recognized to be a failure, patients will be included in the clinical trial after informed consent and randomized in the two strategies based on donor search:
- Reference group: Unrelated Donor group
- Investigational group: Haplo Donor Group
Investigators will use a composite end-point embracing the three main causes of failure: death, relapse and severe cGVHD (as a surrogate endpoint for QOL). We will analyze the HSCT usual objectives as GHVD, NRM, relapse and survival. A specific study of patients' health related quality of life will also be conducted using the FACT-BMT questionnaire. In addition, the success of the two strategies in term of transplant completion (donor determination, transplant realization and time to do so) will be compared.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| HAPLO graft | Experimental | Biological: Allogeneic (Allo) hematopoietic stem cell transplantationConditioning regimen * Fludarabin : 30 mg/m2/day for 4 days: from D-5 à J-2. * Busulfan IV : 130 mg/m2/day for 2 days : drom D-4 to D-3. + 1 day of Thiotepa : 5mg/kg at D-6. Prophylaxis regimen for GVHD * F CSA and MMF (starting day +5) * Additional immunosuppression: PT-HDCy (50 mg/kg/day) on days +3 and +4 Hematopoietic Stem Cell Graft PBSC graft will be preferred for a minimal targeted cell dose of 4 x 106 CD34+cells/kg GCSF (Neupogen ®) during 4 to 5 days (D-4 to D-1): SC 10 µg/kg/d. |
| MUD graft | Active comparator | Biological: Allogeneic (Allo) hematopoietic stem cell transplantationConditioning regimen * Fludarabin : 30 mg/m2/day for 5 days: from D-6 to D-2. * Busulfan IV : 130 mg/m2/day for 2 days: from D-4 to D-3. Prophylaxis regimen for GVHD * CSA and MMF will be used from day -1 after UD * Additional immunosuppression: Rabbit ATG (2.5 mg/kg/day) on days -3 and -2 Hematopoietic Stem Cell Graft PBSC graft will be preferred for a minimal targeted cell dose of 4 x 106 CD34+cells/kg |
Who may qualify
- Ages
- 55 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Patients aged of 55 years or up to 70 years.
- Patients with hematological malignancy
- Patients without a matched related donor
- Patients eligible for an allogeneic HSCT from an alternative donor
- Able to comply with the protocol
Key exclusion criteria (6 listed)
- Clinical or biological contraindication to allogeneic HSCT
- Other evolutive cancer
- Positive serology for HIV, hepatitis B or chronic active hepatitis C
- Pregnant or breast-feeding women.
- Emergency
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 |
|---|---|---|
| Allogeneic (Allo) hematopoietic stem cell transplantation | Biological | HAPLO graft, MUD graft |
Primary outcome
Event-free survival with death, relapse or occurrence of severe cGVHD as event whatever occurs first
Time frame: 5 years
7 secondary outcomes
Engraftment: time to reach 0.5 x 109/l ANC, 20 x 109/l platelets and full donor lymphoid chimerism
Time frame: 5 years
Acute and chronic GVHD cumulative incidences
Time frame: 5 years
Non-relapse mortality cumulative incidence
Time frame: 5 years
Relapse incidence
Time frame: 5 years
Probabilities of overall survival and progression-free survival
Time frame: 5 years
Evaluation of HRQL including patients who relapse
Time frame: 5 years
Evaluation of procedure costs from beginning of search until death or two-year follow-up
Time frame: 5 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Oct 2026.
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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.
Didier Blaise, MD principal investigator
Institut Paoli-Calmettes
14 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Allogeneic (Allo) hematopoietic stem cell transplantation in people with Hematologic Neoplasms, run by Institut Paoli-Calmettes at 14 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 6 exclusion criteria. 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: finished, as of the sponsor's last update on 16 Oct 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 France. 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 phase mean?
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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Event-free survival with death, relapse or occurrence of severe cGVHD as event whatever occurs first (time frame: 5 years). 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 16 Oct 2026.