Myelodysplastic NeoplasmNCT07825207
Observational Study on Eltrombopag in Hypocellular Myelodysplastic Neoplasms
An observational study of Myelodysplastic Neoplasm and Myelodysplastic Syndrome, run by Fondazione Italiana Sindromi Mielodisplastiche-ETS at 26 sites in Italy.
Trial summary
Hypocellular myelodysplastic neoplasms (h-MDS) are a distinct entity introduced in the 2022 WHO classification. They are characterized by reduced bone marrow cellularity and may share several clinical, morphological, immunological, and molecular features with aplastic anemia (AA), making the differential diagnosis… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Myelodysplastic Neoplasm, Myelodysplastic Syndrome
- What is being tested?
- Eltrombopag (ELT)
- How many people
- 100 participants
- Where
- 26 sitesItaly
- Study dates
- 1 May 2026to 31 Jul 2027
- Phase
- Observational
- 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
Study population: Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag included in FISiM registry
Who may be able to join
- Adult patients (i.e. aged ≥18 years) diagnosed with MDS-h according to WHO 2022
- IPSS-R risk very-low to intermediate
- De novo or therapy related MDS
- Availability of bone marrow sample for central revision
- Treatment with eltrombopag, in monotherapy or associated with IST, as first -line therapy or as a subsequent therapy to the first line
Who cannot join
- Unavailability of bone marrow sample for central revision
Trial locations and contacts
26 sites in 1 country.
26 sites in 1 country
Italy26 sites
SCDU di Ematologia, AO SS. Antonio e Biagio e Cesare Arrigo
Alessandria
UO Ematologia con Trapianto, Dipartimento di Medicina di Precisione e Rigenerativa e Area Ionica, AOU Consorziale Policlinico, Università degli Studi Aldo Moro
Bari
Istituto di Ematologia L. e A. Seràgnoli, Policlinico di S. Orsola, IRCCS AOU di Bologna
Bologna
Comprehensive Cancer Center, Spedali Civili di Brescia
Brescia
Oncologia Medica, INOC
Candiolo
MDS Unit, AOU Careggi
Florence
UO Ematologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino
Genova
SC Immunoematologia e Medicina Trasfusionale, Ospedale Carlo Poma, ASST di Mantova
Mantua
Hematology Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori
Meldola (FC)
Oncoematologia, PO Fatebenefratelli, ASST Fatebenefratelli Sacco
Milan
SC Medicina II, PO San Paolo, ASST Santi Paolo e Carlo
Milan
Unità di Ematologia e TMO, IRCCS Ospedale San Raffaele
Milan
UOC Ematologia, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Milan
UOC Ematologia, Dipartimento di Medicina Clinica e Chirurgia, Università di Napoli Federico II
Naples
SCDU Medicina interna ad indirizzo ematologico, AOU San Luigi Gonzaga, Università degli Studi di Torino
Orbassano
UO Ematologia e Immunologia clinica, Dipartimento di Medicina, AOU di Padova
Padova
UOC Ematologia e CTMO, AOU Parma
Parma
UO Ematologia e CTMO, Ospedale Guglielmo da Saliceto
Piacenza
UOC Ematologia, Ospedale S. Eugenio, ASL Roma 2
Roma
Ematologia, Dipartimento di Medicina, Chirurgia e Farmacia, Università degli Studi di Sassari
Sassari
SC Ematologia U, AOU Città della Salute e della Scienza, Università degli Studi di Torino
Torino
SC Ematologia, Dipartimento di Oncologia, AOU Città della Salute e della Scienza
Torino
SCDU Ematologia e Terapie cellulari, AO Ordine Mauriziano, Università degli Studi di Torino
Torino
UOC Ematologia e TMO, Pia Fondazione di Culto e Religione Card. G. Panico
Tricase
UOC Ematologia, Ospedale Maggiore, ASU Giuliano Isontina
Trieste
Hematology Unit, Ospedale di Circolo e Fondazione Macchi, ASST Sette Laghi
Varese
About this study
Hypocellular myelodysplastic neoplasms (h-MDS) are a distinct entity introduced in the 2022 WHO classification. They are characterized by reduced bone marrow cellularity and may share several clinical, morphological, immunological, and molecular features with aplastic anemia (AA), making the differential diagnosis between the two conditions challenging.
Eltrombopag, a thrombopoietin receptor agonist, has demonstrated efficacy in patients with severe AA and has also shown activity in lower-risk MDS, with bone marrow hypocellularity identified as a potential predictor of response. In Italy, eltrombopag has been used off-label in patients with h-MDS and clinically relevant cytopenias. However, systematic real-world data on its effectiveness and safety in this patient population, either as monotherapy or in combination with immunosuppressive therapy (IST), remain limited.
Read more
This is an observational study. We plan to analyse all patients with h-MDS consecutively diagnosed and included in the FISIM registry in 26 Italian centres.
Study duration: 12 months Data to be collected: demographic, disease characteristics at diagnosis (blood count, morphology, histopathology, cytogenetics, multiparameter flow cytometry, presence of PNH clone, molecular data), response to treatment according to IWG criteria, progression to AML rate and survival.
Centralized revision of bone marrow biopsy: bone marrow biopsy at diagnosis will be centrally reviewed
Read the detailed description
Myelodyspastic neoplasms (MDS) are a heterogeneous group of clonal haematopoietic stem cell disorders characterised by ineffective haematopoiesis, morphological dysplasia and a variable risk of transformation into acute myeloid leukaemia (AML). These diseases generally occur in the elderly, with a median age of onset above 70 years.
Recently, major advances in molecular technology and the development of next-generation sequencing (NGS) have deepened our understanding of MDS pathobiology. Hence, the International Consensus Classification (ICC), and the World Health Organization (WHO) proposed in 2022 a revision to the current classification system.
Hypocellular MDS (h-MDS), defined as a bone marrow cellularity of less than 30% in individuals younger than 60 years of age or less than 20% in those older than 70 years, is a new entity included in the WHO-2022 classification but not present in the ICC, accounting for 10-27% of all MDS cases (2,5-7).
The different prevalences of h-MDS are reported because derive from heterogeneity across the studies in the criteria used to define bone marrow hypocellularity, or the inclusion of de novo or both de novo and secondary cases, or differences in genetic and environmental backgrounds among the populations studied and in the possible contamination with patients with aplastic anaemia (AA). Hypocellular MDS are characterized by bone marrow hypoplasia, a low rate of progression to acute myeloid leukemia (AML), and poor response to conventional MDS therapies. For at least some types of AA and MDS, the overwhelming body of evidence points to a shared pathogenesis and, more speculatively, a shared etiology.
The pathogenesis of h-MDS involves immune system activation against hemopoietic precursor, which may explain the favourable response to immunosuppressive therapy.
Recently, based on clinical features and immunologic and molecular studies, two phenotypes of h-MDS were identified and proposed: one with prevailing inflammation and immune activation defined AA-like, and the other characterized by genetic lesions, clonal selection and clonal evolution, named MDS-like.
Differential diagnosis between h-MDS and AA can be difficult as the two pathologies have partially overlapping diagnostic criteria (8,9). Although cellularity easily differentiates h-MDS from normo/hypercellular cases, the distinction from AA is harder when only clinical features are considered. The presence of >10% dysplasia of one lineage would distinguish h-MDS from AA in hypercellular cases and MDS from Idiopatic Cytopenia of Unknown Significance (ICUS). Compared to AA patients, h-MDS are usually older, show marrow dysplasia, and display more BM blasts and more frequent cytogenetic or molecular alterations. The occasional presence of PNH clones in the setting of h-MDS may point toward the diagnosis of AA. Cytogenetic abnormalities are found in about 50% of MDS and FISH analysis could help to better define category group including chromosome 3, 5, and 7 alterations.
Mutational pattern of h-MDS seems to overlap with the classic MDS pattern except for the relative absence of spliceosoma mutations or myeloproliferative features (SRSF2, ZRSR2, U2AF1) and lower frequency of RUNX1, ASXL1, DNMT3A, EZH2, and TP53 mutations.
Using the Internationally Prognostic Scoring System (IPSS) and its revised version (IPSS-R) , h-MDS are classified as low risk and associated with more favourable outcome versus non h-MDS The treatment options used were mainly directed at controlling cytopenias rather than eradication of disease. Lower Risk patients are commonly treated with lower intensity therapies such as hematopoietic growth factors or immunomodulatory agents, while hypomethylating agents, cytotoxic agents, or allo-HCT are typically reserved for higher risk patients.
In some series a hypocellular marrow predicted a higher likelihood of response, analogous to the response to immunosuppressive therapy (IST) in aplastic anemia.
Younger age, normal karyotype or trisomy 8, lack of transfusion dependence, and the presence of a PNH clone predicted response to immunosuppressive therapy, but none is a robust biomarker as responses have also been noted in lower risk MDS patients without these features.
Beyond IST therapy, thrombopoietin receptor agonists (TPO-RA have been studied in MDS with variable response rates.
Eltrombopag, a TPO-RA, was first used to treat thrombocytopenia in patients with idiopathic thrombocytopenic purpura, but has also been shown to improve hematologic response in patients with refractory severe AA and to increase overall and complete responses when combined with standard immunosuppression in treatment-naïve severe AA.
In a phase III study eltrombopag has shown activity in low risk MDS with thrombocytopenia. In a phase II study on 25 LR-MDS patients eltrombopag lead to a bilineage response in 44% of patients and hypocellularity was a predictor of response.
On the basis of this encouraging data eltrombopag has been used in Italy in h_MDS with clinically relevant cytopenias off-label. Data on eltrombopag use outside from clinical trials in a real-world setting, alone or in combination with other IST are missing.
- Conditions
- Myelodysplastic Neoplasm, Myelodysplastic Syndrome
- Being tested
- Eltrombopag (ELT)
- Keywords
- Hypocellular Myelodysplastic Neoplasms, Eltrombopag, Thrombocytopenia, myelodysplastic Syndrome
- Medical subject headings
- Anemia, Refractory, with Excess of Blasts, Myelodysplastic Syndromes, Thrombocytopenia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Eltrombopag (ELT)Drug
Eltrombopag administered as part of routine clinical practice for the treatment of hypocellular myelodysplastic neoplasms. The study retrospectively and prospectively evaluates the effectiveness and safety of eltrombopag in patients treated with eltrombopag monotherapy or in combination with immunosuppressive therapy.
| Study group | Role | What they receive |
|---|---|---|
| Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag | Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag included in FISiM registry
* IPSS-R very-low to intermediate
* De novo or therapy related Available bone marrow sample for central revision Receives: Drug: Eltrombopag (ELT) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Overall Response Rate (ORR)
Overall response rate to eltrombopag according to the International Working Group (IWG) response criteria (Cheson 2006)
Measured: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.
Secondary outcomes (6)
Overall Response Rate (ORR) of eltrombopag combined with immunosuppressive drugs
Overall response rate to eltrombopag when administered in combination with immunosuppressive drugs.
Measured: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.
Overall Survival (OS)
Overall survival from diagnosis and from initiation of eltrombopag treatment.
Measured: From diagnosis and from initiation of eltrombopag treatment until death or last available follow-up, up to study completion.
Duration of Response (DoR)
Duration of response to eltrombopag.
Measured: From achievement of response until loss of response, death, or last available follow-up, up to study completion.
Adverse Events (AE) and Serious Adverse Events (SAE)
Percentage of participants experiencing adverse events and serious adverse events reported in relation to eltrombopag treatment.
Measured: From initiation of eltrombopag treatment through the end of treatment, up to study completion.
Acute Myeloid Leukemia (AML) Rate
Rate of progression to acute myeloid leukemia.
Measured: From diagnosis through study completion.
Time to AML Progression
Time to progression to acute myeloid leukemia from diagnosis and from initiation of eltrombopag treatment
Measured: From diagnosis and from initiation of eltrombopag treatment until AML progression or last available follow-up, up to study completion.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Sep 2026
- Study start1 May 2026
- Primary completion30 Nov 2026 (estimated)
- Study completion31 Jul 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Myelodysplastic NeoplasmStudies 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
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Fondazione Italiana Sindromi Mielodisplastiche-ETS
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Elena Crisà, MD, Principal investigator, INOC
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07825207
- Sponsor's protocol ID
- FISiM-Eltrombopag-hMDS
- Status last verified
- Sep 2026
- First submitted
- 11 Sep 2026
- Last updated
- 17 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- Individual data sharing
- No: for national regulations
Study at a glance
From the registry record, last updated by the sponsor on 17 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Observational Study on Eltrombopag in Hypocellular Myelodysplastic Neoplasms
- ClinicalTrials.gov ID
- NCT07825207
- Acronym / sponsor ID
- FISiM-Eltrombopag-hMDS
- Conditions
- Myelodysplastic Neoplasm, Myelodysplastic Syndrome
- Keywords
- Hypocellular Myelodysplastic Neoplasms, Eltrombopag, Thrombocytopenia, myelodysplastic Syndrome
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Fondazione Italiana Sindromi Mielodisplastiche-ETSUniversity, hospital or other
- Study start
- 1 May 2026 (actual)
- Primary completion
- 30 Nov 2026 (estimated)
- Study completion
- 31 Jul 2027 (estimated)
- First posted
- 17 Sep 2026 (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.
Hypocellular myelodysplastic neoplasms (h-MDS) are a distinct entity introduced in the 2022 WHO classification. They are characterized by reduced bone marrow cellularity and may share several clinical, morphological, immunological, and molecular features with aplastic anemia (AA), making the differential diagnosis between the two conditions challenging.
Eltrombopag, a thrombopoietin receptor agonist, has demonstrated efficacy in patients with severe AA and has also shown activity in lower-risk MDS, with bone marrow hypocellularity identified as a potential predictor of response. In Italy, eltrombopag has been used off-label in patients with h-MDS and clinically relevant cytopenias. However, systematic real-world data on its effectiveness and safety in this patient population, either as monotherapy or in combination with immunosuppressive therapy (IST), remain limited.
This is an observational study. We plan to analyse all patients with h-MDS consecutively diagnosed and included in the FISIM registry in 26 Italian centres.
Study duration: 12 months Data to be collected: demographic, disease characteristics at diagnosis (blood count, morphology, histopathology, cytogenetics, multiparameter flow cytometry, presence of PNH clone, molecular data), response to treatment according to IWG criteria, progression to AML rate and survival.
Centralized revision of bone marrow biopsy: bone marrow biopsy at diagnosis will be centrally reviewed
Detailed description
Myelodyspastic neoplasms (MDS) are a heterogeneous group of clonal haematopoietic stem cell disorders characterised by ineffective haematopoiesis, morphological dysplasia and a variable risk of transformation into acute myeloid leukaemia (AML). These diseases generally occur in the elderly, with a median age of onset above 70 years.
Recently, major advances in molecular technology and the development of next-generation sequencing (NGS) have deepened our understanding of MDS pathobiology. Hence, the International Consensus Classification (ICC), and the World Health Organization (WHO) proposed in 2022 a revision to the current classification system.
Hypocellular MDS (h-MDS), defined as a bone marrow cellularity of less than 30% in individuals younger than 60 years of age or less than 20% in those older than 70 years, is a new entity included in the WHO-2022 classification but not present in the ICC, accounting for 10-27% of all MDS cases (2,5-7).
The different prevalences of h-MDS are reported because derive from heterogeneity across the studies in the criteria used to define bone marrow hypocellularity, or the inclusion of de novo or both de novo and secondary cases, or differences in genetic and environmental backgrounds among the populations studied and in the possible contamination with patients with aplastic anaemia (AA). Hypocellular MDS are characterized by bone marrow hypoplasia, a low rate of progression to acute myeloid leukemia (AML), and poor response to conventional MDS therapies. For at least some types of AA and MDS, the overwhelming body of evidence points to a shared pathogenesis and, more speculatively, a shared etiology.
The pathogenesis of h-MDS involves immune system activation against hemopoietic precursor, which may explain the favourable response to immunosuppressive therapy.
Recently, based on clinical features and immunologic and molecular studies, two phenotypes of h-MDS were identified and proposed: one with prevailing inflammation and immune activation defined AA-like, and the other characterized by genetic lesions, clonal selection and clonal evolution, named MDS-like.
Differential diagnosis between h-MDS and AA can be difficult as the two pathologies have partially overlapping diagnostic criteria (8,9). Although cellularity easily differentiates h-MDS from normo/hypercellular cases, the distinction from AA is harder when only clinical features are considered. The presence of >10% dysplasia of one lineage would distinguish h-MDS from AA in hypercellular cases and MDS from Idiopatic Cytopenia of Unknown Significance (ICUS). Compared to AA patients, h-MDS are usually older, show marrow dysplasia, and display more BM blasts and more frequent cytogenetic or molecular alterations. The occasional presence of PNH clones in the setting of h-MDS may point toward the diagnosis of AA. Cytogenetic abnormalities are found in about 50% of MDS and FISH analysis could help to better define category group including chromosome 3, 5, and 7 alterations.
Mutational pattern of h-MDS seems to overlap with the classic MDS pattern except for the relative absence of spliceosoma mutations or myeloproliferative features (SRSF2, ZRSR2, U2AF1) and lower frequency of RUNX1, ASXL1, DNMT3A, EZH2, and TP53 mutations.
Using the Internationally Prognostic Scoring System (IPSS) and its revised version (IPSS-R) , h-MDS are classified as low risk and associated with more favourable outcome versus non h-MDS The treatment options used were mainly directed at controlling cytopenias rather than eradication of disease. Lower Risk patients are commonly treated with lower intensity therapies such as hematopoietic growth factors or immunomodulatory agents, while hypomethylating agents, cytotoxic agents, or allo-HCT are typically reserved for higher risk patients.
In some series a hypocellular marrow predicted a higher likelihood of response, analogous to the response to immunosuppressive therapy (IST) in aplastic anemia.
Younger age, normal karyotype or trisomy 8, lack of transfusion dependence, and the presence of a PNH clone predicted response to immunosuppressive therapy, but none is a robust biomarker as responses have also been noted in lower risk MDS patients without these features.
Beyond IST therapy, thrombopoietin receptor agonists (TPO-RA have been studied in MDS with variable response rates.
Eltrombopag, a TPO-RA, was first used to treat thrombocytopenia in patients with idiopathic thrombocytopenic purpura, but has also been shown to improve hematologic response in patients with refractory severe AA and to increase overall and complete responses when combined with standard immunosuppression in treatment-naïve severe AA.
In a phase III study eltrombopag has shown activity in low risk MDS with thrombocytopenia. In a phase II study on 25 LR-MDS patients eltrombopag lead to a bilineage response in 44% of patients and hypocellularity was a predictor of response.
On the basis of this encouraging data eltrombopag has been used in Italy in h_MDS with clinically relevant cytopenias off-label. Data on eltrombopag use outside from clinical trials in a real-world setting, alone or in combination with other IST are missing.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag | – | Drug: Eltrombopag (ELT)Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag included in FISiM registry * IPSS-R very-low to intermediate * De novo or therapy related Available bone marrow sample for central revision |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag included in FISiM registry
Key inclusion criteria (5 listed)
- Adult patients (i.e. aged ≥18 years) diagnosed with MDS-h according to WHO 2022
- IPSS-R risk very-low to intermediate
- De novo or therapy related MDS
- Availability of bone marrow sample for central revision
- Treatment with eltrombopag, in monotherapy or associated with IST, as first -line therapy or as a subsequent therapy to the first line
Key exclusion criteria (1 listed)
- Unavailability of bone marrow sample for central revision
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 |
|---|---|---|
| Eltrombopag (ELT)Eltrombopag administered as part of routine clinical practice for the treatment of hypocellular myelodysplastic neoplasms. The study retrospectively and prospectively evaluates the effectiveness and safety of eltrombopag in patients treated with eltrombopag monotherapy or in combination with immunosuppressive therapy. | Drug | Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag |
Primary outcome
Overall Response Rate (ORR)
Time frame: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.
Overall response rate to eltrombopag according to the International Working Group (IWG) response criteria (Cheson 2006)
6 secondary outcomes
Overall Response Rate (ORR) of eltrombopag combined with immunosuppressive drugs
Time frame: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.
Overall Survival (OS)
Time frame: From diagnosis and from initiation of eltrombopag treatment until death or last available follow-up, up to study completion.
Duration of Response (DoR)
Time frame: From achievement of response until loss of response, death, or last available follow-up, up to study completion.
Adverse Events (AE) and Serious Adverse Events (SAE)
Time frame: From initiation of eltrombopag treatment through the end of treatment, up to study completion.
Acute Myeloid Leukemia (AML) Rate
Time frame: From diagnosis through study completion.
Time to AML Progression
Time frame: From diagnosis and from initiation of eltrombopag treatment until AML progression or last available follow-up, up to study completion.
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 17 Sep 2026.
- Individual participant dataSharing planned: No. for national regulations
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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.
Elena Crisà, MD principal investigator
INOC
26 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Myelodysplastic Neoplasm and Myelodysplastic Syndrome, run by Fondazione Italiana Sindromi Mielodisplastiche-ETS at 26 sites in Italy.
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 5 inclusion and 1 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: under way, not looking for participants, as of the sponsor's last update on 17 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 26 sites in Italy. 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?
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 Response Rate (ORR) (time frame: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.). 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 17 Sep 2026.