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Spots Global Cancer Trial Database for A Study of PSMA ADC in Subjects With Metastatic Castration-resistant Prostate Cancer (mCRPC)

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Trial Identification

Brief Title: A Study of PSMA ADC in Subjects With Metastatic Castration-resistant Prostate Cancer (mCRPC)

Official Title: A Phase 2, Open-label, Multicenter Study of PSMA ADC in Subjects With Metastatic Castration-resistant Prostate Cancer

Study ID: NCT01695044

Conditions

Prostate Cancer

Interventions

PSMA ADC

Study Description

Brief Summary: PSMA ADC 2301 is a Phase 2, open-label, study to assess the anti-tumor activity and tolerability of Prostate Specific Membrane Antigen Antibody Drug Conjugate (PSMA ADC) in two groups of subjects with metastatic castration-resistant prostate cancer (mCRPC). One group comprises subjects who must have received at least one taxane-containing chemotherapy regimen (e.g. docetaxel, cabazitaxel). The second group comprises subjects who are cytotoxic chemotherapy-naïve. Subjects who are cytotoxic chemotherapy-naïve must have received and progressed on-, be ineligible for, refused, have an intolerance to-, or not have access to Radium-223. Both groups of subjects must also have received and progressed on abiraterone acetate and/or enzalutamide. If a subject is unable to receive abiraterone acetate and/or enzalutamide, Sponsor approval is required for participation in the study. Subjects will receive up to eight doses of PSMA ADC approximately once every three weeks.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

, Birmingham, Alabama, United States

, Tucson, Arizona, United States

, Burbank, California, United States

, Encinitas, California, United States

, Los Angeles, California, United States

, San Diego, California, United States

, Denver, Colorado, United States

, New Haven, Connecticut, United States

, Norwalk, Connecticut, United States

, Port St. Lucie, Florida, United States

, Honolulu, Hawaii, United States

, Fairway, Kansas, United States

, New Orleans, Louisiana, United States

, Baltimore, Maryland, United States

, Baltimore, Maryland, United States

, Rockville, Maryland, United States

, Boston, Massachusetts, United States

, Ann Arbor, Michigan, United States

, Rochester, Minnesota, United States

, Omaha, Nebraska, United States

, Las Vegas, Nevada, United States

, Lake Success, New York, United States

, New York, New York, United States

, Rochester, New York, United States

, Stony Brook, New York, United States

, Huntersville, North Carolina, United States

, Raleigh, North Carolina, United States

, Cleveland, Ohio, United States

, Pittsburgh, Pennsylvania, United States

, Providence, Rhode Island, United States

, Greenville, South Carolina, United States

, Myrtle Beach, South Carolina, United States

, Memphis, Tennessee, United States

, Dallas, Texas, United States

, Norfolk, Virginia, United States

, Seattle, Washington, United States

Contact Details

Name: Vivien Wong, PhD

Affiliation: Progenics Pharmaceuticals, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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