Overview

Study to Assess the Safety and Tolerability of a PARP Inhibitor in Combination With Topotecan

Status:
Completed
Trial end date:
2009-11-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to identify a safe and tolerable dose of the drug KU-0059436 that can be given in combination with topotecan chemotherapy in patients with advanced solid tumours
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AstraZeneca
Collaborator:
KuDOS Pharmaceuticals Limited
Treatments:
Olaparib
Poly(ADP-ribose) Polymerase Inhibitors
Topotecan
Criteria
Inclusion Criteria:

- Histological or cytological diagnosis of advanced solid tumour for which no suitable
effective therapy exists;

- Evaluable disease

- Adequate bone marrow, hepatic and renal function

Exclusion Criteria:

- Any chemotherapy, radiotherapy ( except palliative), endocrine or immunotherapy within
4 weeks prior to entry; major surgery with 4 weeks of entering the study

- Heavily pre treated patient > 2 previous chemotherapy regimens for metastatic disease

- Co-existing active infection