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Study Summary
No. 2008-0228:.......Lymphoma; Solid Tumors......Aung Naing......Investigational Cancer Therapeutics
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Study Summary Title
Study Summary
Number:
2008-0228
Study Title:A Phase I/II, Open Label, Multi-centre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the Tor Kinase Inhibitor AZD8055 Administered Orally to Patients with Advanced Solid Tumours.
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Physician New Patient Referral
Name:Aung NaingPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Investigational Cancer TherapeuticsReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-563-1930
Contact us about clinical trials
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General Information
Disease Group:Lymphoma
Solid Tumors
Supported By:AstraZeneca
Phase of Study:Phase I/Phase IIReturn
Visit:
14 visits to MDACC including screening, on-study visits (up to the end of Cycle
2), and end-of-study visit.
Treatment
Agents:
AZD8055Home Care:N/A
Treatment Loc:Both at MDACC & outside MDACC at one or more Collaborating Sites or Institutions
Estimated
Length of Stay
in Houston:
24-hours on Cycle 1, Day 1 only.
Description/
Intervention:
The goal of this clinical research study is to find the highest tolerable dose
of AZD8055 that can be given to patients with advanced solid tumors, or
lymphomas and provide additional information on any potential side effects
this drug may cause. The study will also look at the levels of AZD8055 in the
body at different time points. This is called pharmacokinetic (PK) testing.
This study will also look at how the level of study drug in your body may
affect the disease. This is called pharmacodynamic (PD) testing. Researchers
will also look at the action of AZD8055 in the body over a period of time and
study whether the drug has a positive effect on the type of cancer that you
have.
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Study Objectives / Outcomes
Primary Objective:
To assess the safety and tolerability of AZD8055 in patients with advanced solid tumors (or lymphomas Part A only).

Secondary Objectives:

  • To determine the pharmacokinetics (PK) of AZD8055 following both single and multiple oral dosing of AZD8055 in patients with advanced solid tumors (or lymphomas Part A only).
  • To obtain a preliminary evaluation of the role of renal excretion in the disposition of AZD8055
  • To evaluate phosphorylation levels of biomarkers such as, but not limited to, AKT and 4EBP1 following treatment with AZD8055 in PBMCs.
  • To investigate possible relationships between plasma AZD8055 concentrations/exposure and changes in safety and pharmacodynamic (PD) parameters.
  • To give an early indication of efficacy by evaluation of tumor size.
  • To determine inhibition of tumor glucose uptake by assessment with FDG-PET (Part A only).

Exploratory Objectives:
  • Optional samples for Biomarker analysis research (Part A):
    • To evaluate phosphorylation levels of S6 in bucal biopsies following treatment with AZD8055.
  • Optional host genetic research:
  • To investigate whether variability in the PK, safety, efficacy or PD results could be explained by differences in genetic variation (host genetic research)
  • Residual samples for Biomarker analysis research
  • To explore potential biomarkers in residual tumor biopsies, plasma and /serum which may influence development of cancer and associated clinical caharcatersiticsand/or response to AZD8055.
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Study Status Information
Study Activation / Registration Date:07/17/2008
IRB Review and Approval Date:06/04/2008
Study Type:Phase Ii Or Phase I/Ii
Recruitment Status:Terminated
Projected Accrual:80
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Provision of signed written informed consent

2) Male or female, aged 18 years or older

3) Cancer which is refractory to standard therapies, or for which no standard therapies exist, or for which the investigator feels no other active therapy is required for the duration of the study. Inclusion is irrespective of stage of disease.

4) Histological or cytological confirmation of an advanced, solid, malignant tumor (or lymphoma, Part A only).

5) WHO performance status 0-2 (those with performance status 2 must have been stable with no deterioration over the previous 2 weeks)

6) Evidence of post-menopausal status, permanent or surgically sterile, or negative serum or urine pregnancy test for female patients of child-bearing potential. Women will be considered post menopausal if they are over 50 years old and have been amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments. Permanent sterilization includes hysterectomy and/or bilateral oopherectomy and/or bilateral salpingectomy but excludes bilateral tubal occlusion.

7) (continued from above) Tubal occlusion is considered a highly effective method of birth control but does not absolutely exclude the possibility of pregnancy. (The term occlusion refers to both occluding and ligating techniques that do not physically remove the oviducts). Women who have undergone tubal occlusion should be managed as if they are of child-bearing potential (eg undergo pregnancy testing as required by the study). Females of reproductive potential are required to use reliable contraception.

8) For Part A of the study, patients with measurable and non-measurable disease (according to RECIST criteria) can be recruited. For Part B of the study, only patients with measurable disease can be recruited.

9) For Part B of the study patients must be able to provide a tumour biopsy.

Exclusion Criteria:1) Laboratory values as listed below (SI Units): ANC <1.5x10^9/L; Platelets <100x10^9/L; Haemoglobin (Hb) <9.0 g/dL; AST (SGOT) or ALT (SGPT) >2.5 x ULN if no demonstrable liver metastases or >5 x ULN in the presence of liver metastases, total bilirubin (TBL) >1.5 x ULN if no demonstrable liver metastases or >3 x ULN in the presence of liver metastases; Serum creatinine >1.5 x ULN or creatinine clearance </= 50 mL/min (measured or calculated by Cockcroft-Gault method);

2) (continued from above) Clinically relevant and treatment resistant abnormalities in potassium, sodium, calcium (corrected for plasma albumin) or magnesium

3) Patients must not have received prior chemotherapy, biological therapy, radiation therapy, androgens, thalidomide, corticosteroids or other investigational anti-cancer therapy within 21 days of entering the trial (not including palliative radiotherapy at focal sites). Patients must have also recovered from previous chemo-associated toxicities to Grade 0-1 (with the exception of alopecia).

4) Treatment with any hemopoietic growth factors (eg G-CSF, GM-CSF) within 2 weeks prior to receiving study drug

5) Active spinal cord compression as evidenced by clinical signs and/or oedema or progressive growth demonstrated by imaging unless treated and stable off steroids for at least 1 month prior to study treatment

6) Patients with a peripheral neuropathy CTCAE grade >1 in the past 4 weeks. Patients with a history of muscle diseases (including dermatomyositis, polymyositis, inclusion body myositis, muscular dystrophy and metabolic myopathy).

7) Family history of myopathy.

8) Past history of brain metastases or current evidence of brain metastases.

9) Any evidence of severe or uncontrolled systemic conditions (eg, severe hepatic impairment, interstitial lung disease [bilateral, diffuse, parenchymal lung disease]) or current unstable or uncompensated respiratory or cardiac conditions which makes it undesirable for the patient to participate in the study or which could jeopardize compliance with the protocol.

10) Patients with pre existing renal disease including glomerulonephritis, nephritic syndrome, Fanconi Syndrome or Renal tubular acidosis.

11) Patients with an abnormal fasting glucose value defined as >126 mg/dL (>7 mmol/L).

12) Patients with manifest Diabetes Type I and II or Erythrocyte-HbA1c >6.5%

13) Patients with uncontrolled hypercholesterolemia (cholesterol > 200 mg/dl) or hypertriglyceridemia (fasting state, triglycerides > 150 mg/dl ) despite lipid-lowering therapy.

14) Evidence of active infection or active bleeding diatheses

15) Patients who have experienced any of the following procedures or conditions in the preceding 12 months: coronary artery bypass graft; angioplasty; vascular stent; myocardial infarction (MI); angina pectoris; congestive heart failure NYHA Grade 2; uncontrolled hypertension (BP>150/90 mmHg despite maximal medical management); ventricular arrhythmias requiring continuous therapy; supraventricular arrhythmias including AF, which are uncontrolled; hemorrhagic or thrombotic stroke, including transient ischemic attacks or any other central nervous system bleeding

16) Patients with an abnormal echocardiogram at baseline (LVEF < 55% and shortening fraction SF <15%).

17) Patients with any history of Torsades de Pointes.

18) Patients with a QTc interval >450ms for men and >470ms for women from an ECG using Fridericia's correction at both screening visit and predose on the first day of dosing.

19) Patients taking concomitant medications known to prolong QT interval or with factors that increase the risk of QT prolongation or arrhythmic events (heart failure, hyperkalemia, personal or family history of long QT syndrome).

20) Uncontrolled severe thyroid hyperfunction (serum TSH < 0.50 mcU/mL) or hypofunction (serum TSH > 5.50 mcU/mL ).

21) Recent major surgery within 4 weeks prior to entry into the study (excluding the placement of vascular access), or minor surgery within 2 weeks of entry into the study.

22) Patients with documented cases of human immunodeficiency virus (HIV) or hepatitis B or C

23) Involvement in the planning and conduct of the study (applies to both AstraZeneca staff and staff at the study site)

24) Previous enrolment into the present study

25) Patients receiving the following potent and moderate inhibitors and inducers of CYP3A4 are excluded if they are taken within the stated washout periods: Inhibitors (competitive): ketoconazole, itraconazole, indinavir, saquinovir, atazanavir, amprenavir, fosamprenavir, troleandomycin, telithromycin, fluconazole, nefazodone, cimetidine, aprepitant, miconazole, fluvoxamine (1 week minimum wash-out period), and amiodarone (27 week minumum wash-out period)

26) (continued from above) Inhibitors (time dependent): erythromycin, clarithromycin, verapamil, ritonavir, diltiazem (2 week minimum wash-out period) Inducers: phenytoin, rifampicin, St. John's wort, carbamazepine, dexamethasone, primidone, griseofulvin, babiturates, troglitazone, pioglitazone, oxcarbazepine, nevirapine, efavirenz, rifabutin (3-week minimum wash-out period) and phenobarbitone (5 week minimum wash-out period)

27) Has any other severe, acute or chronic medical or psychiatric condition or laboratory abnormality that could increase the risk associated with study participation or study drug administration or could interfere with the interpretation of the study results and, in the judgment of the investigator, would make a patient inappropriate for entry in this study.

28) Refractory nausea and vomiting, chronic gastrointestinal diseases (eg inflammatory bowel disease) or significant bowel resection that would preclude adequate absorption

29) Clinical judgement by the Investigator that the patient should not participate in the study

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Links
Registration Number: NCT00731263
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
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Results


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