An Efficacy and Safety Study of Luspatercept (ACE-536) Versus Placebo in Adults Who Require Regular Red Blood Cell Transfusions Due to Beta (β) Thalassemia (BELIEVE)
Erythrocyte Transfusion, Beta-Thalassemia
About this trial
This is an interventional treatment trial for Erythrocyte Transfusion focused on measuring ACE-536, Safety, Efficacy, Placebo, Red Blood Cell Transfusions, Beta -Thalassemia
Eligibility Criteria
Inclusion Criteria:
Subjects must satisfy the following criteria to be enrolled in the study:
- Male or female, ≥18 years of age at the time of signing the informed consent document (ICF).
- Subject must understand and voluntarily sign an Inform Consent Form 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.
- Documented diagnosis of β-thalassemia or Hemoglobin E/β-thalassemia. (β-thalassemia with mutation and/or multiplication of alpha globin is allowed).
Regularly transfused, defined as: 6-20 Red Blood Cell (RBC) units* in the 24 weeks prior to randomization and no transfusion-free period for ≥ 35 days during that period.
* Sites who prescribe transfusions and have the transfusion records only in volumes should use for conversion of volume to units the below criteria, in order to obtain number of units within the last 24 weeks to assess the eligibility: 1 unit in this protocol refers to a quantity of packed RBCs approximately 200-350 mL. (i) sites who use transfusion bags within this range, or ≥ 350 mL, the conversion in units should be done by dividing the volume transfused to the patient by 350 mL, (ii) sites who use transfusion bags < 200 mL, the conversion in units should be done by dividing the volume transfused to the patient by 200 mL.
- Performance status: Eastern Cooperative Oncology Group (ECOG) score of 0 or 1.
A female of childbearing potential (FCBP) for this study is defined as a female who: 1) 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 (ie, has had menses at any time in the preceding 24 consecutive months). FCBP participating in the study must:
- Have two negative pregnancy tests as verified by the Investigator prior to starting study therapy. She must agree to ongoing pregnancy testing during the course of the study, and after end of study treatment. 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) If a FCBP engages in sexual activity that may result in a pregnancy, she must agree to use, and be able to comply with, effective*** contraception without interruption, 28 days prior to starting investigational product, during the study therapy (including dose interruptions), and for 12 weeks (approximately five times the mean terminal half-life of luspatercept based on multiple-dose Pharmacokinetic PK) data) after discontinuation of study therapy.
- True abstinence is acceptable when this is in line with the preferred and usual lifestyle of the subject. [Periodic abstinence (eg, calendar, ovulation, symptothermal, post-ovulation 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 progesterone/progestin containing) hormonal contraception: Oral; Intravaginal; Transdermal; Progestogen/progestin 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.
Male subjects must:
- Practice true abstinence 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 five times the mean terminal half-life of luspatercept based on multiple-dose PK data) following investigational product discontinuation, even if he has undergone a successful vasectomy.
Exclusion Criteria:
The presence of any of the following will exclude a subject from enrollment:
- Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
- Any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study.
- Any condition that confounds the ability to interpret data from the study.
- A diagnosis of Hemoglobin S/β-thalassemia or alpha (α)-thalassemia (eg, Hemoglobin H);
Evidence of active hepatitis C (HCV) infection as demonstrated by a positive HCV-RNA test of sufficient sensitivity, or active infectious hepatitis B as demonstrated by the presence of HBsAg and/or HBVDNA-positive,, or known positive human immunodeficiency virus (HIV).
Note: Subjects receiving antiviral therapies should have 2 negative HCVRNA tests 3 months apart.(ie, one test at the end of the antiviral therapy and a second test 3 months following the first test).
- Deep Vein Thrombosis (DVT) or stroke requiring medical intervention ≤ 24 weeks prior to randomization.
- Use of chronic anticoagulant therapy is excluded, unless the treatment stopped at least 28 days prior to randomization. Anticoagulant therapies used for prophylaxis for surgery or high risk procedures as well as low Molecular Weight (LMW) heparin for superficial venous thrombosis and chronic aspirin are allowed.
- Platelet count > 1000 x 109/L
- Poorly controlled diabetes mellitus within 24 weeks prior to randomization as defined by short term (eg, hyperosmolar or ketoacidotic crisis) and/or history of diabetic cardiovascular complications (eg, stroke or myocardial infarction).
- Treatment with another investigational drug or device ≤ 28 days prior to randomization.
- Prior exposure to sotatercept (ACE-011) or luspatercept (ACE-536).
- Use of an erythropoiesis-stimulating agent (ESA) ≤ 24 weeks prior to randomization.
- Iron chelation therapy, if initiated ≤ 24 weeks prior to randomization (allowed if initiated > 24 weeks before or during treatment).
- Hydroxyurea treatment ≤ 24 weeks prior to randomization.
- Pregnant or lactating females.
- Uncontrolled hypertension. Controlled hypertension for this protocol is considered ≤ Grade 1 according to NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 (current active minor version).
Major organ damage, including:
- Liver disease with alanine aminotransferase (ALT) > 3 x the upper limit of normal (ULN) or history of evidence of cirrhosis;
- Heart disease, heart failure as classified by the New York Heart Association (NYHA) classification 3 or higher, or significant arrhythmia requiring treatment, or recent myocardial infarction within 6 months of randomization.
- Lung disease, including pulmonary fibrosis or pulmonary hypertension which are clinically significant ie, ≥ Grade 3 NCI CTCAE version 4.0 (current active minor version).
- Creatinine clearance < 60 mL/min (per Cockroft-Gault formula).
- Proteinuria ≥ Grade 3 according to NCI CTCAE version 4.0 (current active minor version).
- Chronic systemic glucocorticoids ≤ 12 weeks prior to randomization (physiologic replacement therapy for adrenal insufficiency is allowed). Single day glucocorticoid treatment (eg, for prevention or treatment of transfusion reactions, is allowed).
- Major surgery ≤ 12 weeks prior to randomization (subjects must have completely recovered from any previous surgery prior to randomization).
- History of severe allergic or anaphylactic reactions or hypersensitivity to recombinant proteins or excipients in the investigational product (see Investigator Brochure).
- Cytotoxic agents, immunosuppressants ≤ 28 days prior to randomization (ie, antithymocite globulin (ATG) or cyclosporine)
History of malignancy with the exception of:
- Curatively resected nonmelanoma skin cancer.
- Curatively treated cervical carcinoma in situ.
- Other solid tumor with no known active disease in the opinion of the investigator.
Sites / Locations
- Children's Hospital of Los Angeles
- Children's Hospital and Research Center at Oakland
- Ann and Robert H Lurie Childrens Hospital of Chicago
- Boston Children's Hospital
- Weill Cornell Medical College
- Hospital of the University of Pennsylvania
- Prince of Wales Hospital
- Mater Hospital Brisbane
- Royal Adelaide Hospital Institute of Medical and Veterinary Science
- Monash Medical Centre
- Sir Charles Gairdner Hospital
- Royal Prince Alfred Hospital
- University Mulitiprofile Hospital for Active Treatment Sveti Georgi EAD
- Specialized Hospital for Active Treatment of Haematological Diseases - Sofia
- Multiprofile Hospital for Active Treatment Sveta Marina EAD
- University Health Network
- Hopital Henri Mondor
- GH de Institut Catholique St. VincentHématologie
- Hopitaux de La Timone
- Hospital of Necker
- Laiko General Hospital of Athens
- Local Institution - 405
- General Children's Hospital "Agia Sophia"
- General Hospital Georgios Gennimatas of Athens
- University General Hospital of Patras
- Hippokration Hospital
- Local Institution - 404
- Soroka University Medical Centre
- Rambam Health Corporation
- HaEmek Medical Center
- Shaare Zedek Medical Center
- Hadassah Medical Center
- Galilee Medical Center
- Rabin Medical Center
- Presidio Ospedaliero Antonio Perrino
- Universita degli Studi di Cagliari - ASL8
- Azienda Ospedaliero-Universitaria di Ferrara - Arcispedale Sant'Anna
- Ente Ospedaliero Ospedali Galliera - Centro della Microcitemia e delle Anemie Congenite
- Fondazione Ca Granda IRCCS Ospedale Maggiore
- Seconda Universita Degli Studi Di Napoli
- AORN A Cardarelli
- Azienda Ospedaliero Universitaria S. Luigi Gonzaga
- Azienda Ospedaliera Ospedali Riuniti Villa Sofia-Cervello
- Azienda Ospedaliera Universitaria Integrata Di Verona
- Chronic Care Center
- Hospital Sultanah Aminah
- Hospital Sultanah Bahiyah
- Hospital Raja Permaisuri Bainun
- Queen Elizabeth Hospital
- Hospital Umum Sarawak
- University Malaya Medical Centre
- Hospital Pulau Pinang c/o Penang Medical College
- Changhua Christian Hospital
- Kaohsiung Medical University Hospital
- China Medical University Hospital
- National Taiwan University Hospital
- Chulalongkorn University Faculty of Medicine - King Chulalongkorn Memorial Hospital
- Siriraj Hospital Mahidol University
- Chiang Mai University - Maharaj Nakorn Chiang Mai Hospital
- University Hospital Farhat Hached
- Bone Marrow Transplant Center
- Aziza Othmana Hospital
- Military Hospital of Tunis
- Acibadem Adana Hospital
- Cukurova University Medical Faculty Balcali Hospital
- Local Institution - 524
- Hacettepe Universitesi
- Antalya Egitim Arastirma
- Istanbul Universitesi Istanbul Tip Fakultesi Hastanesi
- Ege Universitesi Tip Fakultesi Hastanesi
- Mersin University Medical Faculty
- St James University Hospital
- University College Hospital Trust
- Barts Health NHS Trust - The Royal London Hospital
- Whittington Hospital
- Manchester Royal Infirmary
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Luspatercept (ACE-536) plus Best Supportive Care (BSC)
Placebo plus Best Supportive Care (BSC)
Luspatercept, subcutaneous(ly) (SC) once every 21 days
normal saline solution subcutaneous(ly) (SC) once every 21 days