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Spots Global Cancer Trial Database for ASCENT: Androgen Independent Prostate Cancer Study of Calcitriol Enhancing Taxotere

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Trial Identification

Brief Title: ASCENT: Androgen Independent Prostate Cancer Study of Calcitriol Enhancing Taxotere

Official Title: A Phase 2/3 Multicenter, Randomized, Double Blind Study of Docetaxel (Taxotere) Plus DN-101 or Placebo in Androgen Independent Prostate Cancer (AIPC)

Study ID: NCT00043576

Conditions

Prostate Cancer

Interventions

calcitriol
docetaxel

Study Description

Brief Summary: The purposes of this study are to determine if DN-101 plus Taxotere lowers PSA levels, delays or limits disease progression and is safe with minimal side effects.

Detailed Description: DN-101 is an investigational drug that has not been approved by the U.S. Food and Drug Administration (FDA). It is a newly formulated pill that contains high amounts of calcitriol, a naturally occurring hormone and the biologically active form of vitamin D. Administration of DN-101 results in much higher blood levels of calcitriol than the body can produce from dietary vitamin D or vitamin D supplements. These higher levels of calcitriol are associated with anti-cancer effects in laboratory models of human cancer. Laboratory models also indicate that calcitriol has synergy with many commonly used chemotherapeutic agents used to treat cancer. Calcitriol, at very low doses, is currently approved for use in patients with chronic kidney failure. DN-101 was specifically designed for cancer and contains 30 times the amount of calcitriol found in the calcitriol pill commercially available today. In order to take an amount of calcitriol equivalent to 1 DN-101 pill, cancer patients would need to swallow 30 pills of the approved, low dose formulation. DN-101 represents a breakthrough in the use of calcitriol in the clinic, because it contains high concentrations of calcitriol and makes it more feasible for patients to stay on regimen.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Montgomery Cancer Center, Montgomery, Alabama, United States

Arizona Cancer Center- Scottsdale, Scottsdale, Arizona, United States

Arizona Cancer Center/Southern Arizona VA HCS, Tucson, Arizona, United States

Arizona Cancer Center- Tucson, Tucson, Arizona, United States

University of Arkansas for Medical Sciences / Central AR VA, Little Rock, Arkansas, United States

Alta Bates Comprehensive Cancer Center, Berkeley, California, United States

California Cancer Care, Greenbrae, California, United States

Tower Hematology Oncology Medical Group, Los Angeles, California, United States

Prostate Oncology Specialist/Pacific Clinical Research, Marina Del Rey, California, United States

UC Davis Comprehensive Cancer Center, Sacramento, California, United States

Southern California Permanente Medical Group, San Diego, California, United States

Sharp Healthcare, San Diego, California, United States

Pacific Hematology Oncology Associates, San Francisco, California, United States

Kaiser- Northern California, Vallejo, California, United States

San Diego Cancer Center, Vista, California, United States

Oncology Hematology Associates, Paudre Calley Cancer Ctr., Fort Collins, Colorado, United States

University of Miami-Sylvester Comprehensive Cancer Center, Miami, Florida, United States

Oncology Hematology Consultants, Sarasota, Florida, United States

Georgia Urology, P.A., Atlanta, Georgia, United States

Georgia Cancer Specialists, Tucker, Georgia, United States

Loyola University Medical, Maywood, Illinois, United States

Midwest Cancer Research Group, Skokie, Illinois, United States

Urologic Associates- P.C., Davenport, Iowa, United States

Oncology Hematology Care, Crestview HIlls, Kentucky, United States

Tulane University Hospital and Clinic, New Orleans, Louisiana, United States

Johns Hopkins University, Baltimore, Maryland, United States

Associates in Oncology Hematology P.C., Rockville, Maryland, United States

Metro Minnesota CCOP, St. Louis Park, Minnesota, United States

Missouri Cancer Associates, Columbia, Missouri, United States

Univ. of Nebraska Medical Center/VA Hospital, Omaha, Nebraska, United States

New Mexico Cancer Care Associates, Santa Fe, New Mexico, United States

Lincoln Medical & Mental Health Center, Bronx, New York, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

Columbia Presbyterian Medical Center, New York, New York, United States

Union State Bank Cancer Center, Nyack, New York, United States

Raleigh Hematology Oncology Clinic, Cary, North Carolina, United States

The Cleveland Clinic Foundation, Taussig Cancer Center, Cleveland, Ohio, United States

Mid Ohio Oncology Hematology, Inc., Columbus, Ohio, United States

Oregon Health & Sciences University, Portland, Oregon, United States

NW Kaiser Permanente Portland, Portland, Oregon, United States

University of Pittsburgh, Pittsburgh, Pennsylvania, United States

Charleston Hematology Oncology, Charleston, South Carolina, United States

Medical University of South Carolina - Hollings Cancer Center, Charleston, South Carolina, United States

University Oncology/ Hematology Associates, Chattanooga, Tennessee, United States

Boston Baskin Cancer Group, Memphis, Tennessee, United States

Professional Quality Research, Austin, Texas, United States

Texas Oncology, P.A., Dallas, Texas, United States

Texas Cancer Care, Fort Worth, Texas, United States

Urology Associates of North Texas, Ft. Worth, Texas, United States

North Texas Regional Cancer Center, Plano, Texas, United States

Tyler Cancer Center, Tyler, Texas, United States

University of Washington Cancer Care, Seattle, Washington, United States

Tom Baker Cancer Centre, Calgary, Alberta, Canada

Cross Cancer Institute, Edmonton, Alberta, Canada

Vancouver Cancer Center, Vancouver, British Columbia, Canada

CancerCare Manitoba, Winnipeg, Manitoba, Canada

London Regional Cancer Centre, London, Ontario, Canada

Ottawa Regional Cancer Centre, Ottawa, Ontario, Canada

Toronto-Sunnybrook Regional Cancer Center, Toronto, Ontario, Canada

Princess Margaret Hospital, University Health Network, Toronto, Ontario, Canada

CHUM / Notre-Dame Hospital, Montreal, Quebec, Canada

Centre hospitalier universitaire de Quebec, Hotel-Dieu de Quebec, Quebec, , Canada

Contact Details

Name: Tomasz Beer, MD

Affiliation: Oregon Health and Science University

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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