Study of PTG-300 in Non-Transfusion Dependent and Transfusion-Dependent Beta-Thalassemia Subjects With Chronic Anemia (TRANSCEND)
β-thalassemia, Ineffective Erythropoiesis, Chronic Anemia
About this trial
This is an interventional treatment trial for β-thalassemia focused on measuring chronic anemia, β-thalassemia
Eligibility Criteria
Main Inclusion Criteria:
- Male and female subjects aged 18 to 65 years, inclusive (Cohorts 1-4b).
- Male and female subjects aged 12-<18 years, with a minimum weight of 30 kg (Cohorts 5 and 6).
- Documented diagnosis of β-thalassemia with no other Hgb abnormality.
Inclusion criteria applicable only for NTD β-thalassemia subjects:
- Mean Hgb < 10.0 g/dL of two measurements (one performed 7-28 days prior to dosing and the other performed within 7 days prior to dosing).
- Requirement of < 6 units RBC transfusion in a 24 week period with the last transfusion at least 8 weeks before screening.
Inclusion criteria applicable only for TD β-thalassemia subjects:
- Transfusion requirement of at least 6 units of RBC in the 24 weeks prior to screening with no transfusion free period > 45 days.
- Last RBC transfusion 5-10 days prior to dosing.
Main Exclusion Criteria:
- Subjects with Sickle Cell disease, Hgb H, Hb Bart's hydrops foetalis or hemoglobin S
- Infection requiring hospitalization or IV antimicrobial therapy, or opportunistic infection within 6 months of dosing, any infection requiring antimicrobial therapy within 2 weeks of dosing; history of infection with human immunodeficiency virus (HIV).
- Subject has a concurrent clinically significant, unstable or uncontrolled cardiovascular, pulmonary, hepatic, renal, gastrointestinal, genitourinary, hematological, coagulation, immunological, endocrine/metabolic or other medical disorder that, in the opinion of the Investigator, might confound the results of the study or pose additional risk to the subject by their participation in the study.
- Known primary or secondary immunodeficiency.
History within 6 months of screening of any of the following:
myocardial infarction, unstable angina, transient ischemic attack, decompensated heart failure requiring hospitalization, congestive heart failure (New York Heart Association Class 3 or 4), uncontrolled arrhythmias, cardiac revascularization, stroke, uncontrolled hypertension (resting systolic blood pressure [BP] > 160mmHg or resting diastolic BP > 100mmHg on more than one occasion) or uncontrolled diabetes (Hgb A1c > 9% or > one episode of severe hypoglycemia).
- Pregnant or lactating females.
Sites / Locations
- UCSF Benioff Children's Hospital
- Boston Children's Hospital
- Hospital of The University of Pennsylvania
- University General Hospital of Patras
- Laiko General Hospital of Athens
- Athens General Hospital 'G Gennimatas'
- Hippokration Hospital
- Presidio Ospedaliero Antonio Perrino
- Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico
- AOU dell'Università degli Studi della Campania Luigi Vanvitelli
- Chronic Care Center
- Hospital Ampang
- Hospital Pulau Pinang
- Hospital Sultanah Aminah
- Queen Elizabeth Hospital
- Hospital Umum Sarawak
- Chulalongkorn University
- Siriraj Hospital Mahidol University
- Maharaj Nakorn Chiang Mai Chiang Mai University
- Khon Kaen University
- Naresuan University
- University Hospital Farhat Hached
- Bone Marrow Transplant Center
- Aziza Othmana Hospital
- Principal Military Hospital
- Acibadem Adana Hospital
- Hacettepe University Medical Faculty
- Akdeniz Universitesi Hastanesi
- Istanbul Universitesi Istanbul Tip Fakultesi Hastanesi
- Ege Universitesi Tip Fakultesi
- Mersin University Medical Facult
- Barts Health NHS Trust
- Barts Health NHS Trust
Arms of the Study
Arm 1
Experimental
PTG-300 Active
Drug: PTG-300 Subcutaneous