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Antiandrogen
Enzalutamide for Prostate Cancer (PROSPER Trial)
Phase 3
Waitlist Available
Research Sponsored by Pfizer
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from randomization until first psa progression (until the data cut-off date of 28 june 2017, maximum duration of treatment: 42.8 months)
Awards & highlights
Pivotal Trial
Summary
This trial is testing a new drug to treat prostate cancer that has not spread. They will be testing how well it works and if it is safe.
Who is the study for?
Men with nonmetastatic, castration-resistant prostate cancer can join this trial. They must be on hormone therapy or have had surgery to lower testosterone levels, have a rising PSA level with a doubling time of 10 months or less, and no signs of the cancer spreading. Participants should be relatively healthy overall, with an expected lifespan of at least one year.
What is being tested?
The study is testing Enzalutamide's effectiveness and safety against a placebo in men whose prostate cancer hasn't spread but continues to grow despite low testosterone levels. The goal is to see if Enzalutamide can help control the disease better than no treatment (placebo).
What are the potential side effects?
Enzalutamide may cause fatigue, back pain, constipation, joint pain, and hot flashes. It might also affect mental function leading to difficulty concentrating or memory problems. Rarely it could increase seizure risk.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from randomization until first psa progression (until the data cut-off date of 28 june 2017, maximum duration of treatment: 42.8 months)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from randomization until first psa progression (until the data cut-off date of 28 june 2017, maximum duration of treatment: 42.8 months)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Metastasis Free Survival (MFS)
Secondary study objectives
Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Global Score
Pharmacotherapy
Chemotherapy-Free Survival
+43 moreSide effects data
From 2017 Phase 4 trial • 215 Patients • NCT0211658234%
Fatigue
25%
Decreased appetite
18%
Asthenia
17%
Back pain
16%
Arthralgia
15%
Nausea
13%
Bone pain
13%
Constipation
13%
Diarrhoea
12%
Pain in extremity
12%
Weight decreased
11%
Anaemia
11%
Musculoskeletal pain
9%
Hypertension
8%
Oedema peripheral
7%
Haematuria
7%
Dizziness
6%
Malignant neoplasm progression
6%
Insomnia
6%
Hot flush
6%
Muscular weakness
5%
General physical health deterioration
5%
Vomiting
5%
Dyspnoea
3%
Spinal cord compression
2%
Renal failure acute
2%
Pulmonary embolism
2%
Pneumonia
1%
Pyrexia
1%
Renal failure
1%
Neutropenia
1%
Cardiac failure
1%
Lower respiratory tract infection
1%
Osteoarthritis
1%
Urinary tract infection
1%
Metastases to central nervous system
1%
Lung disorder
100%
80%
60%
40%
20%
0%
Study treatment Arm
Enzalutamide Total
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: EnzalutamideExperimental Treatment1 Intervention
160 mg by mouth once daily
Group II: PlaceboPlacebo Group1 Intervention
Sugar pill manufactured to mimic enzalutamide 40 mg capsule
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Enzalutamide
2014
Completed Phase 4
~3820
Find a Location
Who is running the clinical trial?
PfizerLead Sponsor
4,649 Previous Clinical Trials
17,742,975 Total Patients Enrolled
42 Trials studying Prostate Cancer
11,438 Patients Enrolled for Prostate Cancer
Astellas Pharma IncIndustry Sponsor
695 Previous Clinical Trials
231,907 Total Patients Enrolled
35 Trials studying Prostate Cancer
7,241 Patients Enrolled for Prostate Cancer
Medivation LLC, a wholly owned subsidiary of Pfizer Inc.Industry Sponsor
21 Previous Clinical Trials
8,532 Total Patients Enrolled
9 Trials studying Prostate Cancer
4,179 Patients Enrolled for Prostate Cancer
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have not had major surgery in the last 4 weeks.I am allergic to certain ingredients in the medication's capsule.My cancer has not spread to other parts of my body.I have brain metastasis or active leptomeningeal disease.My testosterone levels are low, at or below 50 ng/dL.I have not had another invasive cancer in the last 3 years.I have a stomach or intestine condition that affects how my body absorbs food.My cancer has worsened despite hormone therapy.I am currently on hormone therapy for cancer or have had both testicles removed.My prostate cancer is confirmed and does not have certain aggressive features.I have a serious heart condition.I have a history of seizures or conditions that could lead to seizures.My cancer has worsened despite hormone therapy.I can carry out all my daily activities without help.My cancer has not spread to other parts of my body.My prostate cancer is confirmed and does not have certain aggressive features.My prostate cancer does not cause any symptoms.I am currently on hormone therapy for cancer or have had surgery to remove my testicles.I have not used hormonal or biologic therapy for prostate cancer, except for bone agents or GnRH treatments, in the last 4 weeks.I have received chemotherapy before.I am fully active or can carry out light work.My prostate cancer does not cause any symptoms.
Research Study Groups:
This trial has the following groups:- Group 1: Placebo
- Group 2: Enzalutamide
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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