Selumetinib (AZD6244, ARRY-142886) J-BTC Phase 1 Study

A Phase I, Open-Label, Multi-Center Study to Assess the Safety and Tolerability of Selumetinib (AZD6244, ARRY-142886) in Combination With Cisplatin/Gemcitabine in Japanese Patients With Inoperable Locally Advanced or Metastatic Biliary Tract Cancer (BTC)

The objective of this study is to investigate the safety and tolerability of oral dose of selumetinib in combination with chemotherapies (cisplatin and gemcitabine) in Japanese patients with advanced biliary tract cancer (BTC). In addition, the pharmacokinetic (PK) profile of selumetinib and chemotherapies will be investigated. Also, the Maximum tolerated dose (MTD) of selumetinib in combination with chemotherapies for Japanese BTC patients will be identified, if possible.

Study Overview

• Status: Terminated
• Conditions: Inoperable Locally Advanced or Metastatic Biliary Tract Cancer
• Intervention / Treatment: Drug: Cisplatin; Drug: Gemcitabine; Drug: Selumetinib

• Study Type: Interventional
• Enrollment (Actual): 6
• Phase: Phase 1

Contacts and Locations

Study Locations

• Japan
  • Chiba
    • Kashiwa Shi, Chiba, Japan
      • AZD6244 PhI Japanese Gem/
  • Tokyo
    • Chuo Ku, Tokyo, Japan
      • AZD6244 PhI Japanese Gem/

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 20 years to 130 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Provision of written informed consent
2. Patients must be ≥ 20 years
3. Histological or cytological confirmation of locally advanced or metastatic BTC (intra- or extra-hepatic, gallbladder or ampullary carcinoma)
4. Patients who are eligible for treatment with standard dose of cisplatin/gemcitabine combination regimen
5. World Health Organisation (WHO) performance status (PS) 0-1
6. Evidence of post-menopausal status or negative urine/serum pregnancy test for nonmenopausal female patients Women will be considered postmenopausal if they are amenorrheic for 1 year or more without an alternative medical cause. The following age-specific requirements apply: i) Women under 50 years old would be consider postmenopausal if they have been amenorrheic for 1 year or more following cessation of exogenous hormonal treatments and with Luteinizing hormone (LH) and Follicle stimulating hormone (FSH) levels in the post-menopausal range.

ii) Women over 50 years old would be consider postmenopausal if they have been amenorrheic for 1 year or more following cessation of all exogenous hormonal treatments, radiation-induced oophorectomy with last menses > 1 year ago, chemotherapy-induced menopause with >1 year interval since last menses. Or surgical sterilisation (bilateral oophorectomy or hysterectomy). 7. Male patients should be willing to use barrier contraception for a specified period 8. A lesion that can be accurately assessed at baseline by CT or magnetic resonance imaging (MRI) and is suitable for repeated assessment in accordance with RECIST 9. Patients must have a life expectancy ≥16 weeks 10. Patients who can remain in Hospital from Cycle 0 Day 1 up to at least the completion of Cycle 1 Day 9 11. Patient is willing to provide fresh or archival tumour sample and biomarker blood sample.

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Exclusion Criteria:

1. Treatment with any of the following:

   • Nitrosourea or mitomycin C within 6 weeks of the first dose of study treatment
   • Any investigational agents or study drugs from a previous clinical study within 4 weeks of the first dose of study treatment
   • Chemotherapy, immunotherapy or anticancer agents within 3 weeks of the first dose of study treatment
   • selumetinib(therefore, patients who have already participated in this study and been taken selumetinib) or any other MEK(Mitogen-activated protein kinase kinase or Mitogen-activated protein kinase (MAPK) / Extracellular signal-regulated kinase (ERK) kinase) 1/2 inhibitor in past
   • Cisplatin or gemcitabine in past
   • Major surgery (excluding placement of vascular access) within 4 weeks of the first dose of study treatment
   • Radiotherapy with a wide field of radiation within 4 weeks or radiotherapy with a limited field of radiation for palliation within 2 weeks of the first dose of study treatment
2. With the exception of alopecia, any unresolved toxicities from prior therapy ≥Common Terminology Criteria for Adverse Events (CTCAE) Grade 2
3. Spinal cord compression or brain metastases unless asymptomatic, treated and stable and not requiring steroids for at least 4 weeks prior to start of study treatment

4. As judged by the investigator, any evidence of severe or uncontrolled systemic diseases, such as,

   • active bleeding diatheses
   • active infection including hepatitis B, hepatitis C and human immunodeficiency virus (HIV)
   • severe renal impairment, uncontrolled diabetes or renal transplant
   • acute uncontrolled infection
   • current unstable or uncompensated respiratory or cardiac disease
   • peripheral vascular disease including diabetic vasculopathy Screening for chronic conditions is not required

5. Any of the following cardiac criteria:

   • Any factors that increase the risk of QTc prolongation or risk of arrhythmic events (eg, heart failure, hypokalaemia, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years of age or mean resting corrected QT interval (QTc) > 470 msec)
   • Uncontrolled hypertension (BP≥150/95 mmHg despite medical therapy)
   • Acute coronary syndrome within 6 months prior to starting treatment
   • Angina Canadian Cardiovascular Society Grade II-IV (despite medical therapy)
   • Symptomatic heart failure (NYHA [New York Heart Association ] II-IV)
   • Prior or current cardiomyopathy
   • Baseline left ventricular ejection fraction (LVEF) <55% measured by echocardiography or Multiple Gated Acquisition Scan (MUGA)
   • Atrial fibrillation with a ventricular rate >100 bpm at rest
   • Severe valvular heart disease

6. Inadequate bone marrow reserve or organ function as demonstrated by any of the following laboratory values:

   • Absolute neutrophil count < 1.5 x 109/L
   • Platelet count < 100 x 109/L
   • Haemoglobin < 90 g/L
   • Alanine aminotransferase (ALT) > 2.5 times the upper limit of normal (ULN)
   • Aspartate aminotransferase (AST) > 2.5 times ULN
   • Total bilirubin > 1.5 times ULN
   • Creatinine clearance < 50 mL/min (measured or calculated by Cockcroft and Gault equation)

7. Any of the following ophthalmological criteria:

   • Current or past history of central serous retinopathy or retinal vein occlusion
   • Intraocular pressure >21 mmHg
   • Uncontrolled glaucoma (irrespective of intraocular pressure)
8. Inadequate biliary drainage
9. Symptomatic patients with interstitial pneumonitis or lung fibrosis confirmed by plain chest X-ray or chest CT
10. Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of selumetinib
11. History of hypersensitivity to selumetinib or drugs with a similar chemical structure or class to selumetinib
12. History of hypersensitivity to platinum and gemcitabine containing drugs
13. Use of strong CYP(Cytochrome P450)1A2, CYP(Cytochrome P450)2C19 or CYP3A4 inducers and/or inhibitors (for example, but not limited to, fluvoxamine, fluconazole, ticlopidine, ketoconazole, atazanavir, clarithromycin, indinavir, itraconazole, nelfinavir, ritonavir, saquinavir,telithromycin, voriconazole, grapefruit and seville orange or the juices of these fruits, rifampicin, rifabutin, phenytoin, carbamazepine, phenobarbital and St. John's Wort)
14. Any contraindication to the combination chemotherapy as per local prescribing information
15. Judgment by the investigators that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements
16. Involvement in the planning and conduct of the study (applies to both AstraZeneca staff or staff at the study site).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Selumetinib; 25mg/day, 50mg/day and 75mg/day	Drug: Cisplatin; day1 and day8 at each cycle; Drug: Gemcitabine; day1 and day8 at each cycle; Drug: Selumetinib; 25mg/day, 50mg/day and 75mg/day; Other Names: AZD6244

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The Number of Dose-limiting Toxicities	The number of dose-limiting toxicities in selumetinib in combination with cisplatin and gemcitabine	The first cycle with selumetinib until Day 1 of Cycle 2 of combination dosing

Collaborators and Investigators

• Sponsor: AstraZeneca

Study record dates

Study Major Dates

• Study Start: October 1, 2013
• Primary Completion (Actual): August 1, 2014
• Study Completion (Actual): August 1, 2014

Study Registration Dates

• First Submitted: September 10, 2013
• First Submitted That Met QC Criteria: September 21, 2013
• First Posted (Estimate): September 25, 2013

Study Record Updates

• Last Update Posted (Estimate): May 13, 2016
• Last Update Submitted That Met QC Criteria: May 5, 2016
• Last Verified: May 1, 2016

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Digestive System Diseases; Neoplasms; Neoplasms by Site; Digestive System Neoplasms; Biliary Tract Diseases; Biliary Tract Neoplasms; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Anti-Infective Agents; Antiviral Agents; Enzyme Inhibitors; Antimetabolites, Antineoplastic; Antimetabolites; Antineoplastic Agents; Immunosuppressive Agents; Immunologic Factors; Gemcitabine
• Other Study ID Numbers: D1532C00075