Pharmacokinetics, Clinical Trial
— PYRUSOfficial title:
A Phase Ib Multicentre Study of AZD5363 Monotherapy to Assess Anti-Tumour Activity,Safety,Tolerability,and Pharmacokinetics in Patients With Metastatic Castrate-Resistant Prostate Cancer (mCRPC)(PYRUS)
To investigate the safety, tolerability and anti-tumour activity of AZD5363, as monotherapy,
in patients with metastatic Castrate-Resistant Prostate Cancer. AZD5363 will be investigated
in patients who have progressed after chemotherapy (Part A) and in patients who have
progressed before receiving chemotherapy (Part B).
Recruitment into Part A, Group 1 has been suspended. A new design for this group is
currently being evaluated. Part A, group 2 patients (progressed after 1 or more 2nd
generational anti-hormonal therapies) will receive AZD5363 480mg bid intermittently (4 days
on/3days off).
Part B will only start if there is evidence of anti-tumour activity along with AZD5363
having an acceptable safety profile in Part A. Part B will be conducted in pre-chemotherapy
patients on a dose and schedule selected from Part A.
| Status | Completed |
| Enrollment | 59 |
| Est. completion date | June 2014 |
| Est. primary completion date | June 2014 |
| Accepts healthy volunteers | No |
| Gender | Male |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Provision of informed consent - Males aged 18 years and older - Histologically confirmed adenocarcinoma of the prostate without neuroendocrine differentiation or small cell features for which no standard therapy is currently considered appropriate - Documented evidence of Metastatic Castrate-Resistant Prostate Cancer (mCRPC) - Part A: Patients must have received prior docetaxel-based chemotherapy for mCRPC and have a Circulating Tumour Cell score of 5; - Part B: Patients must have progressed before receiving any chemotherapy for mCRPC; Exclusion Criteria: - Any prior exposure to agents which inhibit AKT as the primary pharmacological activity - Any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension, active bleeding diatheses, or active infection including hepatitis B, hepatitis C, and human immunodeficiency virus - Spinal cord compression or brain metastases unless asymptomatic, treated, and stable and not requiring steroids - Clinically significant abnormalities of glucose metabolism - Major surgery within the previous 4 weeks |
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | Research Site | Cardiff, Wales | |
| United Kingdom | Research Site | London | |
| United Kingdom | Research Site | Southampton | |
| United States | Research Site | Ann Arbor | Michigan |
| United States | Research Site | Boston | Massachusetts |
| United States | Research Site | Hackensack | New Jersey |
| United States | Research Site | Nashville | Tennessee |
| United States | Research Site | Sarasota | Florida |
| Lead Sponsor | Collaborator |
|---|---|
| AstraZeneca |
United States, United Kingdom,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Parts A and B: Anti-tumour activity by measurement of changes in circulating prostate-specific antigen (PSA) | PSA measured from baseline for every 4 weeks. Primary assessment is at 12 weeks | No | |
| Primary | Parts A and B: Anti-tumour activity by measurement of changes in circulating tumour cells (CTC) | CTC measured from baseline for every 4 weeks to week 12 (primary assessment) then measured every 12 weeks | No | |
| Primary | Parts A and B: Anti-tumour activity by measurement of malignant soft tissue response rate | Tumour assessments by RECIST v1.1 every 12 weeks from baseline up to disease progression or withdrawal of consent | No | |
| Primary | Parts A and B: Anti-tumour activity by measurement of metastatic bone disease status | Bone lesion assessments by bone scan (PCWG2) criteria every 12 weeks from baseline up to disease progression or withdrawal of consent. | No | |
| Secondary | Parts A and B: Safety and tolerability of AZD5363 in terms of adverse events, serious adverse events (including death) and safety measures: ECG, ECHO/MUGA, physical examination, pulse, blood pressure, weight and laboratory variables | Routine safety assessments, throughout the period that patients receive AZD5363 up to 28 days following discontinuation of study treatment. | Yes | |
| Secondary | Parts A and B: AZD5363 PK: time to maximum plasma concentration, terminal rate constant,terminal half life, area under plasma concentration time curve, plasma clearance & volume of distribution | Multiple AZD5363 PK blood sample assessments.AZD5363 plasma concentration blood samples will be taken on Day 1(pre-dose,2,4,8 hours post-dose);D2(pre-dose);D8(continous) or D11(intermittent) (pre-dose and at 2,4,and 8 hours post-dose);D15,Cyc | No | |
| Secondary | Parts A and B: Plasma concentrations of pharmacodynamic (PD) biomarker | Multiple PD blood sample assessments.PD blood samples will be taken on the same schedule as PK sample and then Day 1 of every 12 weeks thereafter, and at the discontinuation visit | No | |
| Secondary | Parts A and B: Progression-free survival (PFS) | Tumour assessments by RECIST v1.1 every 12 weeks from baseline up to disease progression or withdrawal of consent. | No | |
| Secondary | Parts A and B: Quality of life (QoL) | EORTC QLQ-C15-PAL, EORTC QLQ-PR25, and EORTC QLQ-BM22 Questionnaires | QOL will be documented from date of randomization and for 12 weeks. | No |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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