ProSTAR: A Study Evaluating CPI-1205 in Patients With Metastatic Castration Resistant Prostate Cancer
Status: | Recruiting |
---|---|
Conditions: | Prostate Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/10/2019 |
Start Date: | November 15, 2017 |
End Date: | August 2020 |
Contact: | Debbie Johnson |
Email: | debbie.johnson@constellationpharma.com |
Phone: | 617-714-0555 |
A Phase 1b/2 Study of CPI-1205, a Small Molecule Inhibitor of EZH2, Combined With Enzalutamide or Abiraterone/Prednisone in Patients With Metastatic Castration Resistant Prostate Cancer
This is a two-arm, open label Phase 1b/2 study with an oral administration of CPI-1205 in
combination with either enzalutamide or abiraterone/prednisone in male patients with
metastatic Castration Resistant Prostate Cancer. This study is designed to determine the
maximum tolerated dose (MTD) and recommended Phase II dose (RP2D) based on safety,
tolerability, pharmacokinetic, and efficacy profiles of CPI-1205 in combination with either
enzalutamide or abiraterone/prednisone.
Following determination of MTD and RP2D will proceed to phase 2. Patients in phase 2 will
receive CPI-1205 at the RP2D in combination with either enzalutamide or
abiraterone/prednisone vs either enzalutamide or abiraterone/prednisone as a control arm.
combination with either enzalutamide or abiraterone/prednisone in male patients with
metastatic Castration Resistant Prostate Cancer. This study is designed to determine the
maximum tolerated dose (MTD) and recommended Phase II dose (RP2D) based on safety,
tolerability, pharmacokinetic, and efficacy profiles of CPI-1205 in combination with either
enzalutamide or abiraterone/prednisone.
Following determination of MTD and RP2D will proceed to phase 2. Patients in phase 2 will
receive CPI-1205 at the RP2D in combination with either enzalutamide or
abiraterone/prednisone vs either enzalutamide or abiraterone/prednisone as a control arm.
Inclusion Criteria:
- Adults (Age ≥ 18 years)
- Eastern Cooperative Oncology Group (ECOG) performance status 0-1
- Life expectancy of at least 12 weeks
- Histologically or cytologically confirmed adenocarcinoma of the prostate
- Progressive disease in the setting of medical or surgical castration (i.e. CRPC)
- Documented metastatic disease
- Must have undergone bilateral orchiectomy (surgical castration) or be willing to
continue gonadotropin-releasing hormone (GnRH) analog or antagonist (medical
castration)
- Serum testosterone <50 ng/dL
- Receipt of prior line of second generation androgen inhibitor
- Demonstrate adequate organ function as defined below:
- Absolute Neutrophil Count (ANC) ≥ 1,000/μL
- Platelet Count ≥ 100,000/μL
- Hemoglobin (Hgb) ≥ 8 g/dL
- Serum creatinine ≤ 2 × upper limit of normal (ULN) OR
- Creatinine clearance (CrCl) ≥ 40 mL/min as estimated by the Cockcroft and Gault
formula1 in subjects with creatinine > 2 X ULN
- Bilirubin ≤ 1.5 × ULN unless evidence of Gilbert's disease in which case < 3 x
ULN
- Aspartate aminotransferase (AST) ≤ 2.5 × ULN without liver metastases; must be ≤
5 × ULN with liver metastases
- Alanine aminotransferase (ALT) ≤ 2.5 × ULN without liver metastases; must be ≤ 5
× ULN with liver metastases
Exclusion Criteria:
- Known symptomatic brain metastases (NOTE: patients with treated epidural disease are
allowed)
- Treatment with any of the following for prostate cancer within the indicated timeframe
prior to day 1 of treatment:
1. First generation: AR antagonists (e.g., bicalutamide, nilutamide, flutamide)
within 4 weeks
2. 5 alpha reductase inhibitors, ketoconazole, estrogens (including
diethylstilbesterol [DES]), or progesterones within 2 weeks
3. Chemotherapy within 3 weeks
4. Biologic therapy within 4 weeks
5. Investigational therapy within 3 weeks (or within a time interval less than at
least 5 half-lives of the investigational agent [if known], whichever is longer).
6. Immunotherapy within 4 weeks
7. Prior radionuclide therapy within 4 weeks
We found this trial at
33
sites
9280 W. Sunset Road
Suite 100
Las Vegas, Nevada 89148
Las Vegas, Nevada 89148
702.952.1251
Comprehensive Cancer Centers of Nevada Comprehensive Cancer Centers of Nevada (CCCN) is the award-winning multidisciplinary...
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188 West Northern Lights Boulevard
Anchorage, Alaska 99503
Anchorage, Alaska 99503
Phone: 907-276-1455
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Aurora, Colorado 80045
Phone: 720-848-9383
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University of Maryland As a globally-connected university offering a world-class education, the University of Maryland...
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450 Brookline Ave
Boston, Massachusetts 2215
Boston, Massachusetts 2215
617-632-3000
Phone: 617-632-5701
Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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Rush University Medical Center Rush University Medical Center encompasses a 664-bed hospital serving adults and...
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520 Country Club Dr
Eugene, Oregon 97401
Eugene, Oregon 97401
Phone: 541-683-5001
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Greenville, South Carolina 29605
Phone: 864-455-3600
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UCLA UCLA's primary purpose as a public research university is the creation, dissemination, preservation and...
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823 82nd Parkway, Suite B
Myrtle Beach, South Carolina 29572
Myrtle Beach, South Carolina 29572
(843) 449-1010 ext.268
Carolina Urologic Research Center Carolina Urologic Research Center (CURC) has been recognized both nationally and...
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1430 Tulane Ave Suite SL32
New Orleans, Louisiana 70112
New Orleans, Louisiana 70112
(504) 588-5912
Phone: 504-988-6770
Tulane University Health Sciences Center One of the nation's most recognized centers for medical education,...
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