An Efficacy and Safety Study of Luspatercept (ACE-536) Versus Placebo in Subjects With Myeloproliferative Neoplasm-Associated Myelofibrosis on Concomitant JAK2 Inhibitor Therapy and Who Require Red Blood Cell Transfusions

  • STATUS
    Recruiting
  • End date
    Feb 11, 2025
  • participants needed
    309
  • sponsor
    Celgene
Updated on 10 May 2021

Summary

The purpose of this Phase 3 study is to evaluate the efficacy and safety of Luspatercept compared with placebo in subjects with myeloproliferative neoplasm (MPN)-associated Myelofibrosis (MF) and anemia on concomitant Janus kinase 2 (JAK2) inhibitor therapy and who require red blood cell count (RBC) transfusions.

The study is divided into Screening Period, a Treatment Phase (consisting of a Blinded Core Treatment Period, a Day 169 Response Assessment, a Blinded Extension Treatment Period, and an Open-label Extension Treatment Period), and a Posttreatment Follow-up Period.

Description

Permitted Concomitant Medications and Procedures

  • Subjects are receiving a JAK2 inhibitor for the treatment of MPN-associated MF that is approved in the country where the study is being conducted. JAK2 inhibitors are to be used according to their respective label and as prescribed as part of the subject's standard-of-care therapy as prescribed by their physician prior to study entry.
  • Best supportive care (BSC) includes, but is not limited to, treatment with transfusions (eg, RBC, platelet, whole blood), ICTs, antibiotic, antiviral and/or antifungal therapy, and nutritional support as needed.
  • Granulocyte colony-stimulating factors (ie, G-CSF, granulocyte macrophage colony-stimulating factor [GM-CSF]) are allowed only in cases of neutropenic fever or as clinically indicated per product label.
  • Prophylactic antithrombotic therapy is permitted.
  • Thrombopoietin and platelet transfusions are permitted.
  • Treatment with systemic corticosteroids is permitted for nonhematological conditions providing the subject is receiving a constant dose equivalent to 10 mg prednisone during the study.
  • Administration of attenuated vaccines (eg, influenza vaccine) is allowed if clinically indicated per Investigator discretion.
  • Iron chelation therapy (ICT) is to be used according to the product label. If the label permits, the ICT dose should be stable during at least the first 24 weeks of IP. Initiation of ICT while within the first 24 weeks of IP should be clinically indicated to treat an AE.

Prohibited Concomitant Medications

The following concomitant medications are specifically excluded during the course of the

study
  • Cytotoxic, chemotherapeutic, targeted, or investigational agents/therapies (excluding JAK2 inhibitor therapy)
  • Azacitidine, decitabine, or other hypomethylating agents
  • Lenalidomide, thalidomide, and pomalidomide
  • Erythropoietin stimulating agents (ESAs) and other RBC hematopoietic growth factors (eg, IL-3)
  • Hydroxyurea or other alkylating agents
  • Androgens (unless given to treat hypogonadism)
  • Oral retinoids (topical retinoids are permitted)
  • Arsenic trioxide
  • Interferon
  • Anagrelide
  • Systemic corticosteroids at a dose equivalent to > 10 mg prednisone
  • Investigational products for the treatment of MPN-associated MF

Details
Condition Bone marrow disorder, Blood disorder, Anemia, Myelosclerosis with myeloid metaplasia, MYELOPROLIFERATIVE DISORDER, Post-PV MF, Myeloproliferative Neoplasms, Anemia; Non-Hodgkin’s Lymphoma, Myelofibrosis, Hematological Disorders, Post Polycythemia Vera Myelofibrosis, myeloproliferative neoplasm, myeloproliferative disorders, anaemia
Treatment Placebo, ACE-536
Clinical Study IdentifierNCT04717414
SponsorCelgene
Last Modified on10 May 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Anemia; Non-Hodgkin’s Lymphoma or Myeloproliferative Neoplasms or Blood disorder or Myelofibrosis or Hematological Disorders or Post Polycythemia Vera...?
Do you have any of these conditions: Anemia or Myeloproliferative Neoplasms or myeloproliferative disorders or Bone marrow disorder or myeloproliferative neoplasm or anaemia or Post Polyc...?
Do you have any of these conditions: Myelofibrosis or Post-PV MF or Hematological Disorders or Blood disorder or Anemia or Anemia; Non-Hodgkin’s Lymphoma or Myelosclerosis with myeloid me...?
Do you have any of these conditions: myeloproliferative neoplasm or Anemia or Bone marrow disorder or Myeloproliferative Neoplasms or Hematological Disorders or Post Polycythemia Vera Mye...?
Subjects must satisfy the following criteria to be randomized in the study
Subject is 18 years of age at the time of signing the ICF
Subject has a diagnosis of PMF according to the 2016 World Health Organization (WHO) criteria or diagnosis of post-ET or post-PV MF according to the IWG-MRT 2007 criteria , confirmed by the most recent local pathology report
Subject is requiring RBC transfusions as defined as
Average RBC-transfusion frequency: 4 to 12 RBC units/12 weeks immediately up to randomization. There must be no interval > 6 weeks (42 days) without 1 RBC transfusion
RBC transfusions are scored in determining eligibility when given for treatment of
Symptomatic (ie, fatigue or shortness of breath) anemia with a pretransfusion Hgb 9.5 g/dL or
Asymptomatic anemia with a pretransfusion Hgb 7 g/dL c. RBC transfusions given for worsening of anemia due to bleeding or infections are not scored in determining eligibility
Subjects on continuous (eg, absent of dose interruptions lasting 2 consecutive weeks) JAK2 inhibitor therapy as approved in the country of the study site for the treatment for MPN-associated MF as part of their standard-of-care therapy for at least 32 weeks, on stable daily dose for at least 16 weeks immediately up to the date of randomization and anticipated to be on a stable daily dose of that JAK2 inhibitor for at least 24 weeks after randomization
Subject has an Eastern Cooperative Oncology Group (ECOG) performance score of 2
A female of childbearing potential (FCBP) for this study is defined as a female who
has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (eg, has had menses at any time in the preceding 24 consecutive months). Females of childbearing potential (FCBP)participating in the study must
Have 2 negative pregnancy tests as verified by the Investigator prior to starting study therapy. She must agree to ongoing pregnancy testing during the study, and after end of IP. This applies even if the subject practices true abstinence from heterosexual contact
Either commit to true abstinence _from heterosexual contact (which must be reviewed on a monthly basis and source documented) or agree to use, and be able to comply with, effective contraception_ without interruption, 28 days prior to starting IP, during the study therapy (including dose interruptions), and for 12 weeks (approximately 5 times the mean terminal half-life of IP based on multiple-dose PK data) after discontinuation of study therapy
Male subjects must: Practice true abstinence _(which must be reviewed on a monthly basis) or agree to use a condom during sexual contact with a pregnant female or a female of childbearing potential_ while participating in the study, during dose interruptions and for at least 12 weeks (approximately 5 times the mean terminal half-life of IP based on multiple-dose PK data) following IP discontinuation, even if he has undergone a successful vasectomy
True abstinence is acceptable when it is in line with the preferred and usual lifestyle of the subject. [Periodic abstinence (eg, calendar, ovulation, symptothermal, postovulation methods) and withdrawal are not acceptable methods of contraception.]
Agreement to use highly effective methods of contraception that alone or in
combination result in a failure rate of a Pearl index of less than 1% per year
when used consistently and correctly throughout the course of the study. Such
methods include: Combined (estrogen and progestogen containing) hormonal
contraception: Oral, Intravaginal, Transdermal; Progestogen-only hormonal
contraception associated with inhibition of ovulation: Oral, Injectable
hormonal contraception, Implantable hormonal contraception; Placement of an
intrauterine device (IUD); Placement of an intrauterine hormone-releasing
system (IUS); Bilateral tubal occlusion; Vasectomized partner; Sexual
Abstinence
\. Subject must understand and voluntarily sign an ICF prior to any study-
related assessments/procedures being conducted
\. Subject is willing and able to adhere to the study visit schedule and
other protocol requirements including the use of the electronic patient
reported outcomes device

Exclusion Criteria

The presence of any of the following will exclude a subject from
randomization
Subject with anemia from cause other than MPN-associated MForJAK2 inhibitor therapy (eg, iron deficiency, vitamin B12 and/or folate deficiencies, autoimmune or hemolytic anemia, infection, or any type of known clinically significant bleeding or sequestration)
Subject use of hydroxyurea, immunomodulatory compounds such as pomalidomide, thalidomide, ESAs, androgenic steroids or other drugs with potential effects on hematopoiesis 8 weeks immediately up to the date of randomization
Systemic corticosteroids are permitted for nonhematological conditions providing the subject is receiving a constant dose equivalent to 10 mg prednisone for the 4 weeks immediately up to randomization
Iron chelation therapy (ICT) is permitted providing the subject is receiving a stable dose for the 8 weeks immediately up to randomization
Subject with any of the following laboratory abnormalities at screening
Neutrophils: < 1 x 109/L
White blood count (WBC): > 100 x 109/L
Platelets: the lowest allowable level as approved for the concomitant JAK2 inhibitor but not < 25 x 109/L or > 1000 x 109/L
Peripheral blood myeloblasts:> 5%
Estimated glomerular filtration rate:< 40 mL/min/1.73 m2 (via the 4-variable modification of diet in renal disease [MDRD] formula) or nephrotic subjects (eg, urine albumin-to-creatinine ratio > 3500 mg/g)
Aspartate aminotransferase (AST) or alanine aminotransferase (ALT):> 3.0 x upper limit of normal (ULN)
Direct bilirubin: 2 x ULN
Higher levels are acceptable if these can be attributed to active red blood cell precursor destruction within the bone marrow (eg, ineffective erythropoiesis)
Subject with uncontrolled hypertension, defined as repeated elevations of systolic blood pressure 140 mmHg or diastolic blood pressure 90 mmHg, that is not resolved at the time of randomization
Subject with prior history of malignancies, other than disease under study, unless the subject has been free of the disease for 3 years. However, subject with the following history/concurrent conditions is allowed
Basal or squamous cell carcinoma of the skin
Carcinoma in situ of the cervix
Carcinoma in situ of the breast
Incidental histologic finding of prostate cancer (T1a or T1b using the tumor, nodes, metastasis [TNM] clinical staging system)
Subject with prior hematopoietic cell transplant or subject anticipated to receive a hematopoietic cell transplant during the 24 weeks from the date of randomization. 7. Subject with stroke, myocardial infarction, deep venous thrombosis, pulmonary or arterial embolism within 6 months immediately up to the date of randomization
Subject with major surgery within 2 months up to the date of randomization. Subject must have completely recovered from any previous surgery immediately up to the date of randomization
Subject with a major bleeding event (defined as symptomatic bleeding in a critical area or organ and/or bleeding causing a decrease in Hgb of 2 g/dL or leading to transfusion of 2 units of packed red cells) in the last 6 months prior to the date of randomization
Subject with inadequately controlled heart disease and/or have a known left
ventricular ejection fraction < 35%
Subject with uncontrolled systemic fungal, bacterial, or viral infection
(defined as ongoing signs/symptoms related to the infection without
improvement despite appropriate antibiotics, antiviral therapy, and/or other
treatment)
Subject with known human immunodeficiency virus (HIV), evidence of active
Hepatitis B (HepB) as demonstrated by the presence of Hepatitis B surface
antigen (HBsAg) and/or positive for Hepatitis B virus DNA (HBVDNA-positive)
and/or evidence of active Hepatitis C (HepC) as demonstrated by a positive
Hepatitis C virus RNA (HCV-RNA) test of sufficient sensitivity
Subject with prior therapy of luspatercept or sotatercept. 14.Subject with
history of severe allergic or anaphylactic reactions or hypersensitivity to
recombinant proteins or excipients in the investigational product
Pregnant or breastfeeding females. 16.Subject participation in any other
clinical protocol or investigational trial that involves use of experimental
therapy (including investigational agents) and/or therapeutic devices within
days or for investigational agents within five half-lives, whichever comes
later, immediately up to the date of randomization
Subject with any significant medical condition, laboratory abnormality
psychiatric illness, or is considered vulnerable by local regulations (eg
imprisoned or institutionalized) that would prevent the subject from
participating in the study or places the subject at unacceptable risk if
he/she were to participate in the study. 18.Subject with any condition or
concomitant medication that confounds the ability to interpret data from the
study
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