A Phase II Study of Oral Tamibarotene in Acute Promyelocytic Leukemia Patients Who Have Received Prior Therapy with ATRA and Arsenic Trioxide (STAR-1) - STAR-1

Conditions: Acute Promyelocytic Leukemia
MedDRA version: 9.1Level: LLTClassification code 10001019Term: Acute promyelocytic leukaemia

Registration Number: EUCTR2007-002183-99-IT

Lead Sponsor: INNOVIVE PHARMACEUTICALS

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Recruiting

Sex: All

Target Recruitment: 50

Inclusion Criteria

Patients must meet all of the following criteria for admission into the study: (1) Have a diagnosis of either relapsed and/or refractory APL: - Refractory disease is defined as a confirmed diagnosis of APL and a myeloblast plus promyelocyte count of >10% in the bone marrow in patients who have failed to respond to induction therapy in the first or second line setting. Induction therapy must have included ATRA- and ATO-based therapy given either sequentially or in combination. - Relapsed disease is defined as a confirmed diagnosis of APL and a myeloblast plus promyelocyte count of >10% in the bone marrow following a documented complete remission or positive RT-PCR assay for PML/RAR-alfa in two consecutive tests separated by at least one month, after treatment with ATRA- and ATO-based therapy given either sequentially or in combination. (2) Confirmation of diagnosis and relapsed/refractory APL must be obtained in blood or bone marrow mononuclear cells by at least one of the following methods: - Conventional cytogenetics showing the translocation t(15:17), - Positive RT-PCR assay for PML/RAR-alfa;, or - Fluorescence in situ hybridization (FISH) analysis showing evidence of the PML/RAR-alfa translocation. (3) Patients must have received and failed therapy with ATRA and ATO either within the same or separate induction/consolidation schedule(s). Treatment must have been administered for a minimum of 28 days for each agent. Treatment may have been administered either as combination therapy or sequentially as single agents. Patients who failed to complete a course of induction/consolidation therapy, as specified, due to drug intolerance are eligible for the study. (4) Patients in whom ATO is contraindicated (for example due to congenital long QT syndrome) are eligible for inclusion on study if they have received and failed ATRA therapy as defined in (3). (5) Be able to provide written informed consent prior to enrollment into the study (see Appendix D). (6) Be magior equal to 18 years old. (7) Have an Eastern Cooperative Oncology Group (ECOG) Performance Status of minor equal to 2 (see Appendix B). (8) Have an estimated life expectancy of major equal to 12 weeks. (9) Be male or a non-pregnant, non-lactating female. Fertile patients must agree to use an effective barrier method of contraception (e.g., latex condom, diaphragm, or cervical cap) to avoid pregnancy while on therapy and for 90 days following the discontinuation of the study drug. [In countries where double barrier contraception is required by Regulatory Authorities, patients who are fertile must agree to use 2 forms of barrier method contraception (e.g., latex condom AND a diaphragm or cervical cap) while on therapy and for 90 days following the discontinuation of the study drug.] A non-fertile female is defined as: - Postmenopausal (amenorrheic for major equal to 12 months) - Undergone a complete oophorectomy or hysterectomy. (10) Have a negative serum or urine pregnancy test within 10 days prior to the first dose of study drug (if patient is a female of childbearing potential). (11) Have adequate organ function as indicated by the following laboratory values obtained within 10 days prior to the first dose of study drug as outlined in Table 2. Table 2 Inclusion Laboratory Values Parameter Required Value (units) Hepatic Serum bilirubin minor equal to 1.5 x ULN without leukemic involvement (minor equal to 3.0 x ULN with leukemic

Exclusion Criteria

Patients who meet any of the following criteria will be excluded from study admission: (1) Extramedullary leukemia. (2) Patients on a vitamin A preparation or patients with hypervitaminosis A. (3) Have received cytotoxic therapy minor equal to 2 weeks from the start of therapy. If the patient needs these agents due to urgent medical care within 2 weeks prior to starting tamibarotene, a waiver may be granted by the INNOVIVE Medical Monitor. (4) Have a history of myelodysplastic syndromes (MDS). (5) Have impaired cardiac function or clinically significant heart disease including: - myocardial infarction within 3 months, unstable angina pectoris, congenital long QT syndrome and clinically significant resting bradycardia (<50 beats per minute), uncontrolled congestive heart failure, uncontrolled hypertension, history of labile hypertension, or history of poor compliance with antihypertensive medication. (6) Have an active, uncontrolled systemic infection considered opportunistic, life-threatening, or clinically significant at the time of treatment. (7) Have clinically significant acute or chronic liver or renal disease considered unrelated to leukemia. (8) Have uncontrolled hyperlipidemia. (9) Have uncontrolled or poorly controlled diabetes mellitus. (10) Have impaired gastrointestinal function that may significantly alter drug absorption (e.g., uncontrolled vomiting, ulcerative colitis, malabsorption, or small bowel resection). (11) Are pregnant or lactating. (12) Have psychiatric disorder(s) that would interfere with consent, study participation, or follow-up. (13) Have not recovered from acute toxicities of all previous therapy prior to enrollment. (14) Have any other severe concurrent disease and/or uncontrolled medical conditions, which, in the judgment of the investigator, could predispose patients to unacceptable safety risks or compromise compliance with the protocol. (15) Have a history of another primary malignancy that has been actively treated in the last 24 months. (16) Are unwilling or unable to comply with the protocol.