AnemiaPhase 2NCT01736683
Study of Sotatercept for the Treatment of Anemia in low-or Intermediate-1 Risk Myelodysplastic Syndromes (MDS) or Non-proliferative Chronic Myelomonocytic Leukemia (CMML)
A Phase 2 study testing Sotatercept in people with Anemia and Myelodysplastic Syndromes, run by Merck Sharp & Dohme LLC at 20 sites in 2 countries.
Trial summary
The primary objective of this study is to determine a safe, tolerable and effective dose of sotatercept that results in the greatest frequency of improvement of anemia in patients diagnosed with low- or intermediate-1 risk myelodysplastic syndromes (MDS) or non-proliferative chronic myelomonocytic leukemia (CMML). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Anemia, Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia
- What is being tested?
- Sotatercept
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 74 participants
- Where
- 20 sitesin 2 countries
- Study dates
- 28 Nov 2012to 30 Apr 2018
- Phase
- Phase 2
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Men and women ≥ 18 years of age
- Documented diagnosis of myelodysplastic syndromes (MDS) or non-proliferative chronic myelomonocytic leukemia (CMML), white blood cells (WBC) ≤ 13,000 /mm^3, World Health Organization (WHO) that meets International Prognostic Scoring System (IPSS) criteria for low or intermediate-1 risk disease
- Anemia, Hemoglobin (Hgb) ≤ 9.0 g/dL or ≥ 2 units of Red Blood Cells (RBCs) within 84 days
- No response or loss of response to Erythropoiesis-Stimulating Agents (ESAs) or erythropoetin (EPO) > 500 mU/ml
- Eastern Cooperative Group (ECOG) score ≤2.
- Creatinine < 1.5 * Upper Limit of the Normal (ULN)
Show all 10Show fewer
- Total bilirubin ≤3.0 mg/dL
- Aspartate aminotransferase (AST)/Serum glutamic oxaloacetic transaminase (SGOT) \& Alanine Aminotransferase (ALT)/Serum Glutamic Pyruvic (SGPT) ≤3.0 * Upper Limit of Norma (ULN)
- Free of metastatic malignancy (other than MDS) for ≥2 years
- Highly effective methods of birth control for females and males
Who cannot join
- Chromosome 5q deletion
- Pregnant or breast feeding women and males who do not agree to use condom during the sexual contact with females of childbearing potential
- Major surgery within 30 days
- Incomplete recovery or incomplete healing of wounds from previous surgery
- Heart failure ≥3 (New York Heart Association (NYHA))
- Thromboembolic or myocardial infarction event within 6 months
Show all 15Show fewer
- Concurrent anti-cancer cytotoxic chemotherapy
- History of severe allergic or anaphylactic reaction or hypersensitivity to recombinant protein
- Known positive for Human Immunovirus (HIV) or infectious Hepatitis type C or active infectious Hepatitis type B
- Clinically significant anemia unrelated to MDS
- Thrombocytopenia (<30,000/uL)
- Uncontrolled hypertension
- Treatment with another investigational drug or device within 28 days prior to Day 1
- Prior exposure to sotatercept (ACE-011)
- Any serious medical condition, lab abnormality or psychiatric illness
Trial locations and contacts
20 sites in 2 countries.
20 sites in 2 countries
United States13 sites
Johns Hopkins
Baltimore, Maryland, 21231
Dana-Farber / Harvard Cancer Institute
Boston, Massachusetts, 02215
The Cleveland Clinic Foundation Hematology and Medical Oncology Rm 35
Cleveland, Ohio, 44195
Rocky Mountain Cancer Center-Midtown
Denver, Colorado, 80218
Monter Cancer Center, North Shore LIJ Health Systems
Lake Success, New York, 11042
Sarah Cannon Research Inst
Nashville, Tennessee, 37203
Columbia University Medical Center/New York-Presbyterian Hospital
New York, New York, 10032
Virginia Oncology Associates
Norfolk, Virginia, 23502
Texas Oncology Round Rock Cancer Center - Round Rock
Round Rock, Texas, 78681
University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229
H. Lee Moffitt Cancer Center and Research Institute
Tampa, Florida, 33612
Texas Oncology, P.A. - Tyler
Tyler, Texas, 75702
Yakima Valley Memorial Hospital/ North Star Lodge
Yakima, Washington, 98902
France7 sites
Centre Hospitalier Universitaire d'Avicennes
Bobigny, 93009
Institute Paoli-Calmettes Service Haematology
BP 156,, 13273
CHRU de Lille-Hopital Claude Huriez Service des Maladies du Sang
Lille, 59037
CHRU Nantes
Nantes, 44093
Hopital Cochin Hematologie
Paris, 75679
Centre Henri Becquerel
Rouen, 79038
CHU Purpan
Toulouse, 31059
About this study
Official title: An Open-label, Randomized, Phase 2, Parallel, Dose-Ranging, Multicenter Study of Sotatercept for the Treatment of Patients With Anemia and Low or Intermediate-1 Risk Myelodysplastic Syndromes or Non-proliferative Chronic Myelomonocytic Leukemia (CMML)
The primary objective of this study is to determine a safe, tolerable and effective dose of sotatercept that results in the greatest frequency of improvement of anemia in patients diagnosed with low- or intermediate-1 risk myelodysplastic syndromes (MDS) or non-proliferative chronic myelomonocytic leukemia (CMML).
- Conditions
- Anemia, Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia, Low to Intermediate-1 MDS, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML)
- Being tested
- Sotatercept
- Keywords
- ACE-011, anemia, dose-ranging, intermediate-1 risk myelodysplastic syndromes, low risk myelodysplastic syndromes (MDS), multicenter, open-label, parallel, phase 2, randomized, Sotatercept, Non-proliferative chronic myelomonocytic leukemia (CMML), hemoglobin, transfusions
- Medical subject headings
- Anemia, Myelodysplastic Syndromes, Leukemia, Myelomonocytic, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SotaterceptDrug
Also called ACE-011, ActRIIA-IgG1Fc
Sotatercept is supplied as a lyophilized powder that is reconstituted using Water for Injection (WFI) and administered as a subcutaneous injection (SC) injection by the study staff at the clinical site.
| Study group | Role | What they receive |
|---|---|---|
| Sotatercept 0.1 mg/kg | Experimental | Sotatercept 0.1 mg/kg Receives: Drug: Sotatercept |
| Sotatercept 0.3 mg/kg | Experimental | Sotatercept 0.3 mg/kg Receives: Drug: Sotatercept |
| Sotatercept 0.5 mg/kg | Experimental | Sotatercept 0.5 mg/kg Receives: Drug: Sotatercept |
| Sotatercept 1.0 mg/kg | Experimental | Sotatercept 1.0 mg/kg Receives: Drug: Sotatercept |
| Sotatercept 1.5 mg/kg | Experimental | Sotatercept 1.5 mg/kg Receives: Drug: Sotatercept |
| Sotatercept 2.0 mg/kg | Experimental | Sotatercept 2.0 mg/kg Receives: Drug: Sotatercept |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants With Erythroid Hematological Improvement (HI-E) Starting Before the Completion of Five Cycles of Treatment (Responder Rate)
The responder rate includes non-transfusion dependent efficacy (NTDE) participants and transfusion dependent efficacy (TDE) participants. For non-transfusion dependence efficacy (NTDE) participants who required < 4 units of RBCs in the 8 weeks prior to start of therapy, HI-E was defined as an increase of >=1.5 g/dL hemoglobin sustained for 56 days over a period of >=8 weeks. For transfusion dependence efficacy (TDE) participants who required >=4 units of RBCs in the 8 weeks prior to start of therapy, HI-E was defined as a decrease of >= 4 units of RBCs transfused sustained for 56 days over a period of 8 weeks.
Measured: Day 2 to Day 142
Secondary outcomes (10)
Time to Erythroid Hematological Improvement (HI-E) Response
Time to first response = start date of first response (HI-E) - first dose date + 1 day. For NTDE participants (who required < 4 units of RBCs in the 8 weeks prior to start of therapy), HI-E was defined as an increase of >=1.5 g/dL hemoglobin sustained for 56 days over a period of >=8 weeks. For TDE participants (who required >=4 units of RBCs in the 8 weeks prior to start of therapy), HI-E was defined as a decrease of >= 4 units of RBCs transfused sustained for 56 days over a period of 8 weeks.
Measured: Day 1 to Day 87
Duration of Erythroid Hematological Improvement (HI-E)
The duration of HI-E response for participants who responded was (the last date of the consecutive hemoglobin [Hgb] measurements of the first >=56 day interval) - (the first date of the consecutive Hgb measurements of the first >=56 day interval) + 1 day.
Measured: Day 1 to 183.7 weeks
Time to Progression to Acute Myeloid Leukemia (AML) for Participants Who Had Progression
Progression to AML used criteria by the International Working Group (IWG) Response Criteria in Myelodysplasia (Cheson, 2006). Progression is considered if any of the following are met: - >=50% increase in blasts - >=50% decrement from maximum remission/response levels in granulocytes or platelets - Reduction in Hgb concentration by >=2 g/dL - Transfusion dependence This outcome was defined as a Kaplan-Meier estimate however few participants progressed so a Kaplan-Meier analysis could not be performed. Disclosed are time to progression values only for participants who did progress to AML.
Measured: Day 1 to 183.7 weeks
Time to Progression to Events of Higher Risk Myelodysplastic Syndromes (MDS) Using the International Prognostic Scoring System (IPSS) For Participants Who Had Progression
Progression to events of higher risk MDS used criteria from the International Prognostic Scoring System for MDS (IPSS) which assigns a prognostic score (0=good and increasing in risk by half-grades with the top score outlined below) for three prognostic variables: - Marrow blasts (score 0-2.0) - Karyotype (score 0-1.0) - Cytopenias: neutrophil, platelets, and Hg counts (score 0-0.5) The three individual scores are summed resulting in a full range of 0- 3.5 and placed into risk categories 0 = low risk 0.5-1.0 = intermediate-1 risk 1.5-2.0 = intermediate-2 risk >=2.5 = high risk This outcome was defined as a Kaplan-Meier estimate however few participants progressed so a Kaplan-Meier analysis could not be performed. Data reported represent event times (weeks) for participants who did progress to higher risk MDS categories.
Measured: Day 1 to 257.3 weeks
Kaplan-Meier Estimates for Progression-free Survival
Participants who had disease progression were considered to have events. Participants who died without acute myeloid leukemia (AML) were also considered to have events with the event date as the date of death. Those who did not have disease progression and who were lost to follow-up were censored at the last known disease progression assessment date. Participants without disease progression at the last follow-up contact were censored at the date of the last follow-up contact date. Disease Progression to AML used criteria by the International Working Group (IWG) Response Criteria in Myelodysplasia (Cheson, 2006). Progression is considered if any of the following are met: - >=50% increase in blasts - >=50% decrement from maximum remission/response levels in granulocytes or platelets - Reduction in hemoglobin (Hgb) concentration by >=2 g/dL - Transfusion dependence
Measured: Day 1 to 257.3 weeks
Kaplan-Meier Estimates for Overall Survival (OS)
OS was defined as the time between start of treatment and the death/censored date. Participants who died (regardless of the cause of death) were considered to have an event. Participants who were alive at the end of the study, and participants who were lost to follow-up, were censored at the last date when subjects were known to be alive.
Measured: Day 1 to 257.3 weeks
Pharmacokinetic Parameters of Sotatercept: Serum Concentration at Various Study Timepoints
Maximum observed serum concentration, obtained directly from the observed concentration versus time data.
Measured: Cycle 1 Day 8 and !5 up to Cycle 2 Day 1
Participants With Treatment-Emergent Adverse Events (TEAE)
An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a subject during the course of a study. Treatment-emergent adverse events (TEAEs) are defined as any AE occurring or worsening on or after the first treatment of the study medication and within 42 days after the last dose. The severity of AEs was graded based on National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE), Version 4.0 and the scale: Grade 1 = Mild Grade 2 = Moderate Grade 3 = Severe Grade 4 = Life threatening Grade 5 = Death. Relation to study drug was determined by the investigator. A treatment-related TEAE is defined as TEAE which was considered to be related to the study drug and reported as 'Suspected' on the CRF. AEs with a missing relationship were treated as 'treatment-related' in data summaries.
Measured: Day 1 up to 59.2 months
Dose Limiting Toxicities (DLTs)
The following were DLTs if the investigator suspected they were treatment related: 1. Increase to >= 140 mmHg systolic blood pressure 2. Increase to >=90 mmHg diastolic blood pressure 3. Increase to >=140 systolic and increase > 20 mmHg compared to baseline systolic 4. Increase to >=90 mmHg diastolic and increase > 20 mmHg compared to baseline diastolic 5. Introduction of new anti-hypertension medication during treatment 6. Increase in dose of baseline anti-hypertension medication during treatment 7. >= Grade 2 (moderate severity or worse) hypertension as an adverse event
Measured: Day 1 to 59.2 months
Number of Participants Who Achieved Red Blood Cell (RBC)-Transfusion Independence During the Erythroid Hematological Improvement (HI-E) Interval
Number of participants who achieved RBC-independence was defined as participants who required no RBC-transfusions during a 56-day interval of erythroid hematological improvement (HI-E). NTDE = non-transfusion dependence efficacy participants who required < 4 units of RBCs in the 8 weeks prior to start of therapy TDE = transfusion dependence efficacy participants who required >=4 units of RBCs in the 8 weeks prior to start of therapy
Measured: Day 2 to Day 142
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Nov 2012 (estimated)
- Study start28 Nov 2012
- Primary completion30 Apr 2018
- Study completion30 Apr 2018
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 (1)Papers the sponsor has linked to this study.
- Other trials for AnemiaStudies of the same condition, open and under way.
- More trials run by Merck Sharp & Dohme LLCThe 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 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 74 participants (actual)
Sponsor and investigators
- Lead sponsor
- Merck Sharp & Dohme LLC
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Rodrigo Ito, MD, Study director, Celgene Corporation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01736683
- Sponsor's protocol ID
- 7962-017
- Other IDs
- ACE-011-MDS-001, 2012-002601-22
- Status last verified
- Oct 2022
- First submitted
- 27 Nov 2012
- Last updated
- 24 Oct 2022
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- Yes: http://engagezone.msd.com/doc/ProcedureAccessClinicalTrialData.pdf
Publications
Komrokji R, Garcia-Manero G, Ades L, Prebet T, Steensma DP, Jurcic JG, Sekeres MA, Berdeja J, Savona MR, Beyne-Rauzy O, Stamatoullas A, DeZern AE, Delaunay J, Borthakur G, Rifkin R, Boyd TE, Laadem A, Vo B, Zhang J, Puccio-Pick M, Attie KM, Fenaux P, List AF. Sotatercept with long-term extension for the treatment of anaemia in patients with lower-risk myelodysplastic syndromes: a phase 2, dose-ranging trial. Lancet Haematol. 2018 Feb;5(2):e63-e72. doi: 10.1016/S2352-3026(18)30002-4. Epub 2018 Jan 10.
PubMed 29331635
Study at a glance
From the registry record, last updated by the sponsor on 24 Oct 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open-label, Randomized, Phase 2, Parallel, Dose-Ranging, Multicenter Study of Sotatercept for the Treatment of Patients With Anemia and Low or Intermediate-1 Risk Myelodysplastic Syndromes or Non-proliferative Chronic Myelomonocytic Leukemia (CMML)
- ClinicalTrials.gov ID
- NCT01736683
- Acronym / sponsor ID
- 7962-017
- Conditions
- Anemia, Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia, Low to Intermediate-1 MDS, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML)
- Keywords
- ACE-011, anemia, dose-ranging, intermediate-1 risk myelodysplastic syndromes, low risk myelodysplastic syndromes (MDS), multicenter, open-label, parallel
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 74 participants (actual)
- Lead sponsor
- Merck Sharp & Dohme LLCIndustry (pharma, biotech, devices)
- Study start
- 28 Nov 2012 (actual)
- Primary completion
- 30 Apr 2018 (actual)
- Study completion
- 30 Apr 2018 (actual)
- First posted
- 29 Nov 2012 (estimated)
- Results
- Posted 13 Jun 2019
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary objective of this study is to determine a safe, tolerable and effective dose of sotatercept that results in the greatest frequency of improvement of anemia in patients diagnosed with low- or intermediate-1 risk myelodysplastic syndromes (MDS) or non-proliferative chronic myelomonocytic leukemia (CMML).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 6
| Arm | Type | Receives |
|---|---|---|
| Sotatercept 0.1 mg/kg | Experimental | Drug: SotaterceptSotatercept 0.1 mg/kg |
| Sotatercept 0.3 mg/kg | Experimental | Drug: SotaterceptSotatercept 0.3 mg/kg |
| Sotatercept 0.5 mg/kg | Experimental | Drug: SotaterceptSotatercept 0.5 mg/kg |
| Sotatercept 1.0 mg/kg | Experimental | Drug: SotaterceptSotatercept 1.0 mg/kg |
| Sotatercept 1.5 mg/kg | Experimental | Drug: SotaterceptSotatercept 1.5 mg/kg |
| Sotatercept 2.0 mg/kg | Experimental | Drug: SotaterceptSotatercept 2.0 mg/kg |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- Men and women ≥ 18 years of age
- Documented diagnosis of myelodysplastic syndromes (MDS) or non-proliferative chronic myelomonocytic leukemia (CMML), white blood cells (WBC) ≤ 13,000 /mm^3, World Health Organization (WHO) that meets International Prognostic Scoring System (IPSS) criteria for low or intermediate-1 risk disease
- Anemia, Hemoglobin (Hgb) ≤ 9.0 g/dL or ≥ 2 units of Red Blood Cells (RBCs) within 84 days
- No response or loss of response to Erythropoiesis-Stimulating Agents (ESAs) or erythropoetin (EPO) > 500 mU/ml
- Eastern Cooperative Group (ECOG) score ≤2.
Key exclusion criteria (15 listed)
- Chromosome 5q deletion
- Pregnant or breast feeding women and males who do not agree to use condom during the sexual contact with females of childbearing potential
- Major surgery within 30 days
- Incomplete recovery or incomplete healing of wounds from previous surgery
- Heart failure ≥3 (New York Heart Association (NYHA))
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 |
|---|---|---|
| SotaterceptAlso: ACE-011, ActRIIA-IgG1FcSotatercept is supplied as a lyophilized powder that is reconstituted using Water for Injection (WFI) and administered as a subcutaneous injection (SC) injection by the study staff at the clinical site. | Drug | Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg, Sotatercept 0.5 mg/kg, Sotatercept 1.0 mg/kg, Sotatercept 1.5 mg/kg, Sotatercept 2.0 mg/kg |
Primary outcome
Percentage of Participants With Erythroid Hematological Improvement (HI-E) Starting Before the Completion of Five Cycles of Treatment (Responder Rate)
Time frame: Day 2 to Day 142
The responder rate includes non-transfusion dependent efficacy (NTDE) participants and transfusion dependent efficacy (TDE) participants. For non-transfusion dependence efficacy (NTDE) participants who required < 4 units of RBCs in the 8 weeks prior to start of therapy, HI-E was defined as an increase of >=1.5 g/dL hemoglobin sustained for 56 days over a period of >=8 weeks. For transfusion dependence efficacy (TDE) participants who required >=4 units of RBCs in the 8 weeks prior to start of therapy, HI-E was defined as a decrease of >= 4 units of RBCs transfused sustained for 56 days over a period of 8 weeks.
10 secondary outcomes
Time to Erythroid Hematological Improvement (HI-E) Response
Time frame: Day 1 to Day 87
Duration of Erythroid Hematological Improvement (HI-E)
Time frame: Day 1 to 183.7 weeks
Time to Progression to Acute Myeloid Leukemia (AML) for Participants Who Had Progression
Time frame: Day 1 to 183.7 weeks
Time to Progression to Events of Higher Risk Myelodysplastic Syndromes (MDS) Using the International Prognostic Scoring System (IPSS) For Participants Who Had Progression
Time frame: Day 1 to 257.3 weeks
Kaplan-Meier Estimates for Progression-free Survival
Time frame: Day 1 to 257.3 weeks
Kaplan-Meier Estimates for Overall Survival (OS)
Time frame: Day 1 to 257.3 weeks
Pharmacokinetic Parameters of Sotatercept: Serum Concentration at Various Study Timepoints
Time frame: Cycle 1 Day 8 and !5 up to Cycle 2 Day 1
Participants With Treatment-Emergent Adverse Events (TEAE)
Time frame: Day 1 up to 59.2 months
Dose Limiting Toxicities (DLTs)
Time frame: Day 1 to 59.2 months
Number of Participants Who Achieved Red Blood Cell (RBC)-Transfusion Independence During the Erythroid Hematological Improvement (HI-E) Interval
Time frame: Day 2 to Day 142
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Oct 2022.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 29331635Komrokji R, Garcia-Manero G, Ades L, Prebet T, Steensma DP, Jurcic JG, Sekeres MA, Berdeja J, Savona MR, Beyne-Rauzy O, Stamatoullas A, DeZern AE, Delaunay J, Borthakur G, Rifkin R, Boyd TE, Laadem A, Vo B, Zhang J, Puccio-Pick M, Attie KM, Fenaux P, List AF. Sotatercept with long-term extension for the treatment of anaemia in patients with lower-risk myelodysplastic syndromes: a phase 2, dose-ranging trial. Lancet Haematol. 2018 Feb;5(2):e63-e72. doi: 10.1016/S2352-3026(18)30002-4. Epub 2018 Jan 10.
- Individual participant dataSharing planned: Yes. http://engagezone.msd.com/doc/ProcedureAccessClinicalTrialData.pdf
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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.
Rodrigo Ito, MD study director
Celgene Corporation
20 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Sotatercept in people with Anemia and Myelodysplastic Syndromes, run by Merck Sharp & Dohme LLC at 20 sites in 2 countries.
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 10 inclusion and 15 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 24 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 20 sites in United States, 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 13 Jun 2019). 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?
Percentage of Participants With Erythroid Hematological Improvement (HI-E) Starting Before the Completion of Five Cycles of Treatment (Responder Rate) (time frame: Day 2 to Day 142). 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 NCT01736683, which also lists 1 linked publication.
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 24 Oct 2022.