Prostate Cancer Clinical Trial

Study of 18F-DCFPyL PET/CT Imaging in Patients With Suspected Recurrence of Prostate Cancer

Summary

This study evaluates the diagnostic performance and safety of 18F-DCFPyL (PyL) PET/CT imaging in patients with suspected recurrence of prostate cancer who have negative or equivocal findings on conventional imaging.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Male >/= 18 years of age
Histopathologically confirmed prostate adenocarcinoma per original diagnosis, with subsequent definitive therapy

Suspected recurrence of prostate cancer based on rising PSA after definitive therapy on the basis of:

Post-radical prostatectomy: Detectable or rising PSA that is ≥ 0.2 ng/mL with a confirmatory PSA ≥ 0.2 ng/mL (American Urological Association [AUA]); or
Post-radiation therapy, cryotherapy, or brachytherapy: Increase in PSA level that is elevated by ≥ 2 ng/mL above the nadir (American Society for Therapeutic Radiology and Oncology [ASTRO]-Phoenix)
Negative or equivocal findings for prostate cancer on conventional imaging performed as part of standard of care workup within 60 days prior to Day 1
Life expectancy ≥6 months as determined by the investigator
Able and willing to provide informed consent and comply with protocol requirements

Exclusion Criteria:

Subjects administered any high energy (>300 KeV) gamma-emitting radioisotope within five (5) physical half-lives prior to Day 1
Ongoing treatment with any systemic therapy (e.g. ADT, antiandrogen, GnRH, LHRH agonist or antagonist) for prostate cancer
Treatment with ADT in the past 3 months of Day 1
Receipt of investigational therapy for prostate cancer within 60 days of Day 1
Subjects with any medical condition or other circumstances that, in the opinion of the investigator, compromise the safety or compliance of the subject to produce reliable data or completing the study

Study is for people with:

Prostate Cancer

Phase:

Phase 3

Estimated Enrollment:

208

Study ID:

NCT03739684

Recruitment Status:

Completed

Sponsor:

Progenics Pharmaceuticals, Inc.

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There are 14 Locations for this study

See Locations Near You

City of Hope National Medical Center
Duarte California, 91010, United States
Tower Urology
Los Angeles California, 90048, United States
University of California San Francisco - Helen Diller Cancer Center
San Francisco California, 94143, United States
Stanford
Stanford California, 94305, United States
Yale University
New Haven Connecticut, 06520, United States
Moffitt Cancer Center
Tampa Florida, 33612, United States
University of Iowa
Iowa City Iowa, 52242, United States
Johns Hopkins University
Baltimore Maryland, 21287, United States
University of Michigan
Ann Arbor Michigan, 48109, United States
Washington University - Mallinckrodt Institute of Radiology
Saint Louis Missouri, 63110, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States
University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States
University of Wisconsin
Madison Wisconsin, 53705, United States
Chu de Quebec - Universite Laval
Quebec , G1R2J, Canada

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 3

Estimated Enrollment:

208

Study ID:

NCT03739684

Recruitment Status:

Completed

Sponsor:


Progenics Pharmaceuticals, Inc.

How clear is this clinincal trial information?

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