Overview
Study to Assess the Safety and Tolerability of a PARP Inhibitor in Combination With Topotecan
Status:
Completed
Completed
Trial end date:
2009-11-01
2009-11-01
Target enrollment:
0
0
Participant gender:
All
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 tumoursPhase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
AstraZenecaCollaborator:
KuDOS Pharmaceuticals LimitedTreatments:
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