Study to Assess the Safety and Preliminary Efficacy of AZD0156 at Increasing Doses Alone or in Combination With Other Anti-cancer Treatment in Patients With Advanced Cancer.



Status:Recruiting
Conditions:Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 127
Updated:1/5/2019
Start Date:November 10, 2015
End Date:August 30, 2019
Contact:AstraZeneca Clinical Study Information Center
Email:information.center@astrazeneca.com
Phone:1-877-240-9479

Use our guide to learn which trials are right for you!

A Phase I, Open-Label Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of Ascending Doses of AZD0156 Monotherapy or in Combination With Either Cytotoxic Chemotherapies or Novel Anti-Cancer Agents in Patients With Advanced Malignancies

The purpose of this study is to determine whether AZD0156 is safe, what is the best dose to
give, and how it is processed by the body when given alone or in combination with other
agents. The study will also collect some initial information about how effective it is.

The study will consist of a number of study modules, each evaluating the safety and
tolerability of AZD0156 with a specific combination agent. The combination option may require
an initial monotherapy dose escalation to gain an understanding of pharmacokinetics, safety
and tolerability before initiating dose escalation in combination. An oral formulation of
AZD0156 will be used.

Module 1 explores AZD0156 in combination with olaparib Module 2 explores AZD0156 in
combination with irinotecan/FOLFIRI Additional modules may be added to explore AZD0156 as a
monotherapy or in combination with other agents and may be in different tumour types.

Expansion cohorts may enroll additional patients to explore further the safety, tolerability,
pharmacokinetics and biological activity at selected dose(s) or alternate dosing schedules,
and to get a preliminary assessment of efficacy .

Module 1 includes an expansion cohort in locally advanced/metastatic tumours including but
not limited to gastric adenocarcinoma Module 2 includes an expansion cohort in colorectal
cancer

Inclusion criteria for all parts of the study

- Confirmation of locally advanced/metastatic cancer. Refractory or resistant to
standard therapy, or have no effective standard

- Aged at least 18 yrs

- Reasonable health (performance status 0 or 1), stable over the previous 2 weeks

- Females who can have children must use contraception; have a negative pregnancy test,
& not be breast feeding

- Sexually active male patients must use contraception for duration of study and for 3
months afterwards Inclusion criteria for Part B only

- Tumour(s) that can be measured by CT or MRI, at least 1cm in size Inclusion Part B

- Confirmation of metastatic/locally advanced cancer of specific tumour type which
failed to respond to standard treatments Exclusion criteria for all parts of the study

- Prior treatment with an ATM inhibitor

- Past medical history of an inflammatory type(interstitial) lung disease or current
inflammatory lung disease

- Radiotherapy within the last 4 weeks, except palliative radiotherapy for bone pain
relief

- Prior treatment with drugs that may cause lung damage

- Poor of lung function

- History/presence of muscle weakness or abnormal blood tests relating to muscle
function

- Cancer affecting the spinal cord and/or brain unless asymptomatic and stable

- Any evidence of severe or uncontrolled diseases, active bleeding,kidney transplant, or
active infection including liver infections (hepatitis B, hepatitis C) and human
immunodeficiency virus (HIV).

- Evidence of severe lung infections

- Receiving, or having received during the four weeks prior to starting study treatment
other chemotherapy treatment for your cancer

- Treatment with certain doses of steroids during the two weeks prior to starting study
treatment

- A known sensitivity to AZD0156 or any of its components

- Treatment with any unapproved medicine within 28 days prior to starting study
treatment

- Receiving, or having received medications, herbal supplements and/or foods that
significantly affect how your liver works

- Low numbers of certain blood cells

- If your liver and kidney aren't working normally

- If your heart isn't working normally or you have a strong family history of certain
heart diseases

- Other cancers within the past 3 years, except for certain types of cervical and skin
cancers

- Sickness and vomiting, digestive diseases or previous significant bowel removal

- Patients with uncontrolled fitting

- Infections requiring treatment

- Other severe and/or uncontrolled medical conditions in addition to your cancer

- A blockage in your digestive system or severe bleeding from the stomach within 4 weeks
before your take medication on the stuy

- Patients with acute leukaemia or certain bone marrow diseases

- Patients with a known sensitivity to olaparib or its components (Module 1), or
components of FOLFIRI (Module 2)

- Any previous treatment with drugs that work like olaparib. (Module 1 Only)
We found this trial at
3
sites
?
mi
from
New York, NY
Click here to add this to my saved trials
?
mi
from
Aurora, CO
Click here to add this to my saved trials
?
mi
from
Seoul,
Click here to add this to my saved trials