Study Details

A study of MDV3100 to evaluate safety, tolerability, pharmacokinetics and efficacy of in prostate cancer patients

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT01284920

Astellas Study ID

The unique identification code given by the study sponsor.

9785-CL-0111

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

N/A

Condition

Prostate Cancer

Phase

These clinical trials are usually the first time an experimental treatment is studied in a small group of people.

Phase 1

Age

20 years - N/A

Sex

Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Nov 2010 - Jul 2014

Masking

None (Open Label)

Enrollment number

47

A Phase I/II, Open-Label, Uncontrolled, Dose-Escalation Study of MDV3100 in Patients with Castration-Resistant Prostate Cancer

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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