Trial Search Results

Safety, Efficacy, & Pharmacokinetic Study of Tamibarotene to Treat Patients With Relapsed or Refractory APL

This is a Phase II, open-label, non-randomized study to evaluate the safety, efficacy, and pharmacokinetics of tamibarotene in adult patients with relapsed or refractory acute promyelocytic leukemia (APL) following treatment with all-trans-retinoic acid (ATRA) and arsenic trioxide (ATO). Patients must have received and failed therapy with ATRA and ATO. Treatment may have been administered either as combination therapy or sequentially as single agents. Patients who are intolerant to either drug are eligible for this study.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

CytRx

Intervention(s):

  • Drug: Tamibarotene

Phase:

Phase 2

Eligibility


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-α 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-α, or

      - Fluorescence in situ hybridization (FISH) analysis showing evidence of the
      PML/RAR-α 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.

   6. Be ≥ 18 years old.

   7. Have an Eastern Cooperative Oncology Group (ECOG) Performance Status of ≤ 2.

   8. Have an estimated life expectancy of ≥ 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 ≥ 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.

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 ≤ 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.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
650-498-7061
Not Recruiting