Testing SIROLIMUS in Beta-thalassemia Transfusion Dependent Patients (THALA-RAP)

Università degli Studi di Ferrara

Status and phase

Unknown

Phase 2

Conditions

Beta-Thalassemia

Treatments

Drug: Sirolimus 0.5 mg

Study type

Interventional

Funder types

Other

Identifiers

NCT04247750

2018-001469-18 (EudraCT num)

Details and patient eligibility

About

In β-thalassaemia and Sickle Cell Disease (SCD), a significant production of fetal haemoglobin (HbF) may reduce the severity of clinical course and reactivation of γ-globin gene expression in adulthood. HbF induction is one of the best strategies to ameliorate the characteristic symptoms of these diseases. Hydroxyurea (HU) is the only medication, approved by the US Food and Drug Administration, inducing HbF. However, treatments with HU induce sufficient HbF levels in only half of the patients, and side effects including leukopenia and neutropenia are frequently reported. Therefore, novel therapeutic inducers must be identified to develop a personalized treatment in β-thalassaemia and sickle cell anaemia. The availability of new treatments depends on drugs already approved for other indications, and on pharmacokinetics and pharmacovigilance already assessed. Rapamycin (as Sirolimus) is an immunosuppressant agent, approved by the FDA for acute rejection prevention in renal transplant recipients. The ability of this drug to induce γ-globin gene expression in erythroleukemia cell line and erythroid precursors cells (ErPCs) in ß-thalassaemia patients is already known. A clinical investigation on the effects of sirolimus in ß-Thalassaemia aims to evaluate several parameters related to red blood cell status and HbF levels and is a first step for the full clinical development in this new indication.

Full description

The general aim of this protocol is to demonstrate the applicability of a personalised and precision medicine approach in beta-thalassaemia; the clinical trial setting repurposes a drug, namely sirolimus. The presence of high Fetal Hemoglobin (HbF) levels is considered a condition predictive of a favourable outcome in thalassaemia. Its increase induced by pharmacological agents is considered a potential way to improve the clinical status of the patients. In terms of efficacy analysis, the investigators will focus their attention on HbF levels.

Primary objective:

• The suitability evaluation of sirolimus for the treatment of beta-thalassemia patients within the frame of a comprehensive project aimed at the reduction of their transfusions need, with consequent amelioration of their quality of life. The purpose can be achieved through increasing of HbF levels pharmacologically mediated, with verification of a prerequisite, namely the correlation between the induction of HbF in vitro and in vivo in single patients.

Secondary objectives:

To assess the safety of sirolimus and correlation between administered dose and blood levels in beta-thalassemia patients
To assess the influence of sirolimus on transfusion regimen
To assess the effect of sirolimus on the hematopoietic and immune system of thalassemia patients.

Enrollment

45 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients over 18 years of age;
Patients able to understand the informed consent and to sign it before any study procedure;
Patients with β0/β0 and β+/β0 thalassaemia genotype;
Documented diagnosis of major or intermediate thalassemia transfusion-dependent (number of transfusions not less than 8 over the past 12 months before selection);
On regular transfusion since at least 6 years;
Splenectomy performed at least 60 days before selection or spleen largest dimensions < 20 cm as detected by abdominal echography;
Female participants who are surgically sterilised/hysterectomised or post-menopausal for longer than 2 years or female participants of childbearing potential using and/or willing to continue using a medically reliable method of contraception for the entire study duration, such as oral, injectable, or implantable contraceptives, or intrauterine contraceptive devices, or using any other method considered sufficiently reliable by the investigator in individual cases. Patients must be counselled concerning measures to be used to prevent pregnancy and potential toxicities prior to the first dose of sirolimus;
Patient willing to follow all the study requirements and perform all the study visits and to cooperate with the investigator;
Patient followed by the same clinical site since at least 6 months.

Note that patients will be treated with oral sirolimus only in the case their Erythroid Precursor Cells (ErPCs) are responsive to the in vitro treatment with sirolimus according to laboratory-specific definition (≥ 20% increase of HbF in comparison with samples not treated with sirolimus);

Exclusion criteria

Patient treated with hydroxyurea at selection visit or in the last 6 months;
Ongoing treatment with drugs possibly affecting sirolimus actions;
Documented aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3x Upper Limit of Normal (ULN) at selection;
Documented Platelet count <150.000/microliter and >1.000.000/microliter at selection;
Heart failure as classified by the New York Heart Association (NYHA) classification 3 or higher;
Uncontrolled hypertension defined as systolic blood pressure (BP) ≥ 140 mm Hg or diastolic BP ≥ 90 mm Hg;
Significant arrhythmia requiring treatment,
Corrected QT interval> 450 msec on selection ECG;
Ejection fraction <50% by echocardiogram, multiple gated acquisition scan or cardiac magnetic resonance;
Myocardial infarction within 6 months prior to selection;
Positivity for human immunodeficiency virus (HIV) antibody, active hepatitis B (HBV) or hepatitis C (HCV) as demonstrated by the presence of hepatitis B surface antigen (HBsAg) and a positive HCV-RNA test, HBcAb and HBV-DNA positivity
White blood cell [WBC] count <3000 cells per μL and/or Granulocytes <1500/mm3;
Total cholesterol > 240 mg/dl;
Triglycerides > 200 mg/dl;
Proteinuria with urinary protein >1g/24 hrs;
Current participation in another trial with an investigational drug or experimental device, or inclusion in another trial with an investigational drug or experimental device within the preceding month;
Major surgery (including splenectomy) within 60 days before selection (patients must have fully recovered from any previous surgery);
Iron chelation therapy changed in the last 3 months prior to selection (note that Deferiprone is not accepted as a chelation therapy drug in this study while Desferrioxamine and Deferasirox are tolerated at stable dose);
Current treatment with macrolide antibiotics (clarithromycin);
Pregnant or lactating women;
History of severe allergic or anaphylactic reactions or hypersensitivity to excipients in the experimental drug;
Treatment with live vaccines within 90 days preceding the selection;
Subject with history or current malignancies (solid tumours and haematological malignancies) or presence of masses/tumour detected by ultrasound at selection;
Subject with any significant medical condition and/or laboratory abnormality considered by the investigator as not adequately controlled at the time of selection.