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Phase II Study of Olaparib (AZD2281) in Patients with Metastatic/Advanced Urothelial Carcinoma and Other Genitourinary Tumors with DNA-Repair Defects

Clinical Trial Details

This study is being done to determine if the study drug, Olaparib has an effect on urothelial carcinoma or other non-prostate genitourinary cancers in people with DNA-repair changes in their genes.

This study aims to determine if Olaparib is better or worse than the usual approach for urothelial cancer or other non-prostate genitourinary cancers. There is no standard of care for these cancers, but people who are not participating in a study are usually treated with single-drug taxane chemotherapies (e.g. paclitaxel, abraxane, docetaxel).

Olaparib is approved by the U.S. Food and Drug Administration (FDA) and is taken orally.

Participants will receive Olaparib continuously for as long as they respond to the study drug.

Key Eligibility: 
  1. Open to men and women above the age of 18 who have been diagnosed with a non-prostate GU cancer
  2. Participants must not have had prior treatment with Olaparib or history of allergic reactions attributed to compounds similar to Olaparib. 

Detailed eligibility will be reviewed when you contact the study team. 

Study contact by location

Upper East Side - Manhattan

Contact(s)


646-962-2072
guonc@med.cornell.edu

Primary Investigator(s)

Protocol ID(s)

Weill Cornell Medicine IRB #:

2212025439

ClinicalTrials.gov:

NCT03375307

Sponsor:

10144

Status

Open to Enrollment

Age Group

Adult

Sponsor