Overview

This trial is active, not recruiting.

Condition solid tumours
Treatment olaparib tablet dosing
Phase phase 1
Sponsor AstraZeneca
Start date November 2013
End date March 2015
Trial size 57 participants
Trial identifier NCT01894256, 2013-002225-30, D0816C00006

Summary

This is a 2-part study in patients with advanced solid tumours. Part A will investigate the PK of olaparib in patients with mild or moderate renal impairment compared to patients with normal renal function; Part B will allow eligible study patients continued access to olaparib after the PK phase and will provide additional safety data.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification pharmacokinetics study
Intervention model single group assignment
Masking open label
Arm
(Other)
Patients with calculated serum creatinine clearance ≥81 mL/min (using Cockcroft-Gault equation).
olaparib tablet dosing
Part A - single 300mg oral dose olaparib (administered as 2x150mg tablets) Part B - 300mg oral dose olaparib (administered as 2x150mg tablets) bd
(Other)
Patients with calculated serum creatinine clearance 51-80 mL/min (using Cockcroft-Gault equation).
olaparib tablet dosing
Part A - single 300mg oral dose olaparib (administered as 2x150mg tablets) Part B - 300mg oral dose olaparib (administered as 2x150mg tablets) bd
(Other)
Patients with calculated serum creatinine clearance 31-50 mL/min (using Cockcroft-Gault equation).
olaparib tablet dosing
Part A - single 300mg oral dose olaparib (administered as 2x150mg tablets) Part B - 300mg oral dose olaparib (administered as 2x150mg tablets) bd

Primary Outcomes

Measure
Pharmacokinetics of olaparib: maximum olaparib concentration (Cmax)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib : time to maximum concentration (tmax)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib: area under the plasma concentration-time curve from zero to the last measurable time point (AUC0-t)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib : area under the plasma concentration-time curve from zero to infinity (AUC)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib : apparent plasma clearance following oral administration (CL/F)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib : terminal half-life (t½)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib : apparent volume of distribution (Vz/F)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib : terminal rate constant (λz)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.
Pharmacokinetics of olaparib : renal clearance (CLR)
time frame: Blood samples will be collected on Day 1 of Part A at these time points: pre-dose, 0.25,0.5,1,1.5,2,3,4,6,8,12,24,48,72 and 96 hours post-dose.

Secondary Outcomes

Measure
Assessment of the safety and tolerability of olaparib by collection of adverse event reports
time frame: From baseline, every visit until 30 days after last dose, assessed up to 20 months.
Determine safety and tolerability of olaparib by assessment of 12 lead Electrocardiograms
time frame: Part A: baseline, days 1 and 3. Part B: Day 1 then every 4 weeks. Final assessment within 30 days after last dose.
Determine safety and tolerability of olaparib by physical examination
time frame: Part A: baseline, day -1 and within 30 days after last dose. Part B: Day 1.
Determine safety and tolerability of olaparib by assessment of vital signs
time frame: Part A: baseline, days 1,2 and 3. Part B: Days 1,8,15,22,29 then every 4 weeks. Final assessment within 30 days after last dose.
Determine safety and tolerability of olaparib by assessment of body temperature
time frame: Part A: baseline, day 1. Part B: Days 1,8,15,22,29 then every 4 weeks. Final assessment within 30 days after last dose.
Determine safety and tolerability of olaparib by assessment of clinical chemistry results
time frame: Part A: baseline, days -1 and 3. Part B: Days 1,8,15,22,29 then every 4 weeks. Final assessment within 30 days after last dose.
Determine safety and tolerability of olaparib by assessment of haematology results
time frame: Part A: baseline, days -1 and 3. Part B: Days 1,8,15,22,29 then every 4 weeks. Final assessment within 30 days after last dose.
Determine safety and tolerability of olaparib by assessment of urinalysis results
time frame: Part A: baseline, days -1 and 3. Part B: Days 1,8,15,22,29 then every 4 weeks. Final assessment within 30 days after last dose.

Eligibility Criteria

Male or female participants from 18 years up to 75 years old.

Inclusion criteria:- For inclusion in the study as a patient with renal impairment, the following criterion must be met: 1. Patients must have stable renal impairment (moderate or mild), depending on creatinine clearance estimated using the Cockcroft-Gault equation (moderate 31 to 50 mL/min; mild 51 to 80 mL/min), for at least 2 months prior to the start of the study. For inclusion in the study as a patient with normal renal function, the following criterion must be met: 2. Calculated serum creatinine clearance greater than or equal to 81 mL/min (using Cockcroft-Gault equation). All patients must fulfil the following criteria: 3. Provision of written informed consent prior to any study specific procedures . 4. Patients must be greater than or equal to 18 and less than or equal to 75 years of age. 5. Histologically or, where appropriate, cytologically confirmed malignant solid tumour refractory or resistant to standard therapy or for which no suitable effective standard therapy exists. 6. BMI between 18-30 kg/m2. 7. Normal liver and bone marrow function measured within 28 days prior to administration of IP as defined below: Haemoglobin (Hb) greater than or equal to 10.0 g/dL, with no blood transfusions in the previous 28 days. Absolute neutrophil count (ANC) greater than or equal to 1.5 x 109/L. White blood cells (WBC) greater than 3 x 109/L. Platelet count greater than or equal to 100 x 109/L. Total bilirubin less than or equal to 1.5 x institutional upper limit of normal (ULN) (except in the case of Gilbert's disease). Aspartate aminotransferase or serum glutamic oxaloacetic transaminase (AST), alanine aminotransferase or serum glutamic pyruvic transaminase (ALT) less than or equal to 2.5 x institutional ULN unless liver metastases are present in which case it must be less than or equal to 5x ULN. 8. Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 2. 9. Patients must have a life expectancy greater than or equal to 12 weeks. 10. Evidence of non childbearing status for women of childbearing potential, or postmenopausal status: negative urine or serum pregnancy test within 28 days of study treatment, confirmed prior to treatment on Day 1 of the first treatment period in Part A. Postmenopausal is defined as: Amenorrheic for 1 year or more following cessation of exogenous hormonal treatments. Luteinising hormone and follicle-stimulating hormone levels in the postmenopausal range for women under 50 years of age. Radiation-induced oophorectomy with last menses greater than 1 year ago. Chemotherapy-induced menopause with greater than 1 year interval since last menses Surgical sterilisation (bilateral oophorectomy or hysterectomy). 11. Patients are willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations. 12. Patients must be on a stable concomitant medication regimen (with the exception of electrolyte supplements), defined as no changes in medication or in dose within 2 weeks prior to start of olaparib dosing, except for bisphosphonates, denosumab and corticosteroids, which should be stable for at least 4 weeks prior to start of olaparib dosing. Exclusion criteria:- Patients must not enter the study if any of the following exclusion criteria are fulfilled: 1. Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff, its agents and/or staff at the study site). 2. Previous enrolment in the present study. 3. Participation in another clinical study with an investigational medicinal product (IP) during the last 14 days (or a longer period depending on the defined characteristics of the agent used). 4. Renal transplant and end stage renal disease (ESRD) patients. 5. Patients receiving any systemic chemotherapy or radiotherapy (except for palliative reasons) within 2 weeks prior to study treatment (or a longer period depending on the defined characteristics of the agents used). The patient can receive a stable dose of bisphosphonates or denosumab for bone metastases before and during the study as long as these were started at least 4 weeks prior to treatment. 6. Patients who have received or are receiving inhibitors or inducers of CYP3A4 within the washout period. 7. For Part A only, drugs which affect creatinine clearance such as cephalosporin antibiotics, ascorbic acid, trimethoprim, cimetidine and quinine should not be used within the 7 days prior to dosing with olaparib. 8. Treatment in the previous 3 months with any drug known to have a well-defined potential for hepatotoxicity (eg, halothane). 9. Persistent toxicities (greater than or equal to CTCAE Grade 2) caused by previous cancer therapy, excluding alopecia. 10. Patients with myelodysplastic syndrome/acute myeloid leukaemia. 11. Patients with symptomatic uncontrolled brain metastases. A scan to confirm the absence of brain metastases is not required. Patients with asymptomatic brain metastases or with symptomatic but stable brain metastases can receive a stable dose of corticosteroids before and during the study as long as these were started at least 4 weeks prior to treatment. 12. Major surgery within 2 weeks of starting study treatment and patients must have recovered from any effects of major surgery. 13. Patients considered a poor medical risk due to a serious uncontrolled medical disorder, non malignant systemic disease, uncontrolled seizures, or active uncontrolled infection. Examples include, but are not limited to, uncontrolled ventricular arrhythmia, recent (within 3 months) myocardial infarction, uncontrolled major seizure disorder, unstable spinal cord compression, superior vena cava syndrome, extensive bilateral interstitial lung disease on high resolution computer tomography (HRCT) scan, or any psychiatric disorder that prohibits obtaining informed consent. 14. Patients with a history of heart failure or left ventricular dysfunction. 15. Patients who have gastric, gastro-oesophageal or oesophageal cancer. 16. Patients unable to swallow orally administered medication and patients with gastrointestinal disorders or significant gastrointestinal resection likely to interfere with the absorption of olaparib. 17. Breastfeeding women. 18. Immunocompromised patients eg, patients who are known to be serologically positive for human immunodeficiency virus (HIV). 19. Patients with known active hepatic disease (eg, hepatitis B or C). 20. Patients with a known hypersensitivity to olaparib or any of the excipients of the product. 21. Resting ECG at screening with measurable QTc greater than 470 msec at 2 or more time points within a 24 hour period or family history of long QT syndrome. 22. Clinical judgment by the investigator that the patient should not participate in the study.

Additional Information

Official title An Open-label, Non-randomised, Multicentre, Comparative, Phase I Study of the Pharmacokinetics, Safety and Tolerability of Olaparib Following a Single Oral 300 mg Dose to Patients With Advanced Solid Tumours and Normal Renal Function or Renal Impairment
Principal investigator Christian Rolfo
Trial information was received from ClinicalTrials.gov and was last updated in November 2015.
Information provided to ClinicalTrials.gov by AstraZeneca.