Anagrelide Retard in Essential Thrombocythemia

This is a randomised, multicentre, double-blind, active controlled study to compare the efficacy and safety of two different anagrelide formulations in patients with high-risk essential thrombocythemia (ET).

100 patients, either Anagrelide-treated or Anagrelide-naïve, with an indication to receive Thromboreductin® treatment, will be randomized into one of the two investigational medicinal product (IMP) groups (Anagrelide Retard or Thromboreductin®). Treatment allocation will be balanced within stratum (treated/naive) and age classes by central randomization. Naive patients will start with dose level 2 of the IMPs (i.e., 1 mg Thromboreductin® or 2 mg Anagrelide Retard). Anagrelide-treated patients will be switched to the dose level which is closest to the pre-study anagrelide dose at study start. Dose modifications in the titration phase will be done on a weekly basis (up to a maximum of 12 weeks) until "stable platelet counts" on two consecutive visits is achieved.

The periods of the study participation per patient are as follows:

• Screening (up to 7 days prior to randomization), ending with randomization/first IMP dose (Baseline Visit)
• Titration period (weekly visits for up to 12 weeks): to achieve "stable platelet counts" on two consecutive measurements (i.e. weekly visits)
• Maintenance period (weekly visits for 4 weeks): primary endpoint relevant period. The maintenance period for a patient starts at the visit with the second successive platelet count ≤400 G/L (or <600 G/L, if the dose cannot be increased any more due to intolerance or because the maximal dose allowed has already been reached) if the second platelet value measured lies in the range within ± 30% of the value measured at the previous visit.
• End of study (EoS) safety follow-up visit (28 days after the last maintenance visit/EoT for early termination).

Inclusion criteria

• willing and able to give written informed consent prior to any study specific procedures and able to comply with the trial protocol
• confirmed diagnosis of ET according to 2008 WHO diagnostic criteria* (Swerdlow et al, 2008), defined as meeting all four criteria
• at high risk of experiencing ET-related events, indicated for Thromboreductin® treatment as defined by one or more of the following criteria: age ≥ 60 years, platelet counts ≥ 1000 G/L, increase of platelet count ≥ 300 G/L within 3 months, severe thrombohemorrhagic or ischemic symptoms in anamnesis
• either currently treated with anagrelide
• or ET treatment naive
• or anagrelide naive

Exclusion criteria

• Diagnosis of any myeloproliferative disorder other than ET
• Any known cause for a secondary thrombocytosis
• ET currently well controlled by another cytoreductive treatment than Anagrelide and the opportunity to continue to receive this treatment
• ET currently treated with combination of any two of the following agents: anagrelide, hydroxyurea, interferons, busulfan
• Hypersensitivity to either active or non-active ingredients of anagrelide or to any other excipients of the investigational products
• Known hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption
• Cardiovascular disease grade 3 with a negative benefit/risk assessment or grade 4 (South West Oncology Group; Green and Weiss, 1992)
• Clinically significant abnormal laboratory values (excluding markers for ET) in investigator's opinion
• Severe renal insufficiency (creatinine clearance <30 ml/min)
• Moderate to severe hepatic insufficiency (ALT or AST > 5 times upper normal limit [UNL])
• White blood count (WBC) ≥ 15 G/L at screening
• Diagnosis of any malignancy, other than ET (except basal cell and squamous cell carcinomas of the skin and carcinoma in situ of the cervix that have been completely excised and are considered cured), within the last 3 years, or coexisting malignant, systemic disease
• Poorly controlled diabetes mellitus
• Known infection with hepatitis B, hepatitis C or HIV
• Pregnant or lactating women
• Women of childbearing potential or male patients, who have sexual intercourse with females of childbearing potential, not willing to use an effective method of contraception during the study.
• History of drug/alcohol abuse within the previous 2 years
• Participation in another investigational study within 4 weeks prior to informed consent signed or for a longer duration if specified in local regulations
• Any significant psychiatric disorder that, in the opinion of the investigator, might prohibit the understanding and giving of informed consent, or that might prevent the patient from completing the trial.