Roll Over StudY for Patients Who Have Completed a Previous Oncology Study With Olaparib

Prior treatment

• Currently receiving treatment with any prohibited medication(s).
• Local access to commercially-available drug at no cost to the patient is permitted by local regulation.

Other illness

• Permanent discontinuation from the parent study due to toxicity or disease progression.

Other

• Ongoing, unresolved, Grade 3 or above toxicity requiring interruption of treatment at the time of the termination of the parent study.
• Concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study.

• Provision of signed and dated, written ICF.
• Patient is currently deriving clinical benefit, as judged by the Investigator, from continued treatment in an AZ parent study using an AstraZeneca (AZ) compound that has met its endpoints or has otherwise stopped.
• Patient participating in a prior oncology study with an AZ compound in which they received olaparib and are continuing to receive clinical benefit from treatment; the prior study can be an open-label or blinded study, with unblinding at study close.