Santa Monica, California 90404
310-633-8400 http://www.premiereoncology.com mmulay@premiereoncology.com
Premiere Oncology is a center of excellence dedicated to treating cancer by providing comprehensive and holistic clinical care with attention to issues of survivorship and longevity. The group conducts meaningful oncology research with responsibility and integrity. The aim of the research program is to offer the hopes and benefits of cutting edge treatment to patients while generating data of the highest quality. Premiere Oncology is also committed to educating future healthcare leaders in oncology practice and research and providing community education on cancer prevention and treatment opportunities.
In 2004, Lee S. Rosen, M.D. created Premiere Oncology to continue the research he began in 1996 as founder of the Developmental Therapeutics Program at the University of California, Los Angeles (UCLA). Dr. Rosen specializes in the treatment of gastrointestinal and other solid tumors. He is an avid researcher and has been Principal Investigator of pivotal clinical trials of products approved by the United States Food and Drug Administration (FDA) for the treatment of cancer, including Sutent®, Camptosar®, Eloxatin® and Zometa®. Premiere Oncology is located in Santa Monica, California where it is affiliated with the Saint John's Health Center and the John Wayne Cancer Institute.
Premiere Oncology conducts Phase 1, 2 and 3 clinical trials. We offer a wide array of studies for the treatment for all advanced malignancies. We work collaboratively with clinicians across the country to provide their patients with innovative treatments that bridge the gap between established and future therapies. Sponsors with which we have worked include: Amgen, Amplimed, Antigenics, ArQule, Astra Zeneca, Attenuon, Biogen IDEC, Beohringer-Ingelheim, Bristol Myers Squibb, CancerVax, CovX, Dynavax, Eisai, Exelixis, Genentech, Hana Biosciences, Infinity Pharmaceuticals, Kosan, Nektar, Neopharm, Novacea, Peregrine, Pfizer, Raven, Sanofi-Aventis, SGX, SuperGen, Synta, Tempol, Taiho, Tracon, Wyeth, and Ziopharm. These relationships help to ensure that Premiere Oncology has access to the most exciting products being developed for the treatment of cancer.
Lee S. Rosen, MD has a reputation for excellence in the conduct of early stage clinical trials for patients with solid tumors and treatment of patients with gastrointestinal malignancies. He received his B.A. in English Literature from Yale University, a Masters of Public Policy (M.P.P.) from Harvard University's John F. Kennedy School of Government and his Medical Degree from Baylor College of Medicine in Houston, Texas.
Dr. Rosen is a principal investigator for many clinical trials focusing on new cancer drug development (Phase 1). Formerly Assistant Professor in the Division of Hematology-Oncology, Department of Medicine at the University of California, Los Angeles (UCLA), he founded the Developmental Therapeutics Program, a cancer research initiative focused on new drug development. Dr. Rosen has made significant contributions to translational research with angiogenesis inhibitors (a new class of drugs developed to treat cancer by inhibiting development of new blood vessels), signal transduction inhibitors and innovative drug combinations.
As a result of his Phase 1 experience, Dr. Rosen has developed skills pertinent to the treatment of thyroid cancer, sarcomas, and other rare solid tumor types that do not have United States Food and Drug Administration (FDA) approved treatments available. He has led pivotal clinical trials of many products subsequently approved by the FDA for the treatment of cancer including Camptosar (irinotecan HCL injection), Eloxatin (oxaliplatin), Zometa (zoledronic acid for injection) and Sutent (sunitinib malate). In the year 2000, his work with angiogenesis inhibitors was featured on the CBS television program 60 Minutes. He has since treated hundreds of patients with more than a dozen drugs in this class.
Linnea Chap, MD is a highly respected specialist in cancers affecting women. She received her medical degree from the University of Chicago, completed her residency in internal medicine at Northwestern Memorial Hospital and her fellowship in both Hematology and Medical Oncology at UCLA. She joined the faculty at UCLA in 1995 serving most recently as Associate Professor of Medicine and co-director of the UCLA/Revlon Multidisciplinary Breast Center, overseeing the Multidisciplinary Breast Clinic. Dr. Chap has multiple publications to her credit and has led several breast and ovarian cancer treatment protocols, including the pioneering use of novel biologic agents such as Herceptin and Avastin.
In 2001, Dr. Chap was named one of "America's Top Breast Cancer Doctors" by Redbook, a national women's magazine. Annually, she has also been listed as one of "America's Top Doctors for Cancer". Recognized for her teaching and speaking skills, Dr. Chap has a national reputation where she is frequently called on to relate the most recent advances in breast cancer treatment.
Jonathan Goldman, MD graduated magna cum laude from Harvard University and received his medical degree from Stanford University. He completed his residency in internal medicine at University of California San Francisco and his fellowship in both hematology and medical oncology at UCLA.
In addition to seeing all types of hematology and oncology patients, Dr. Goldman will be developing a multidisciplinary thoracic malignancy program in our community.
Premiere Oncology's research staff has a cumulative total of more than 50 years' experience in clinical research, including contracts, budget development, study coordination, and data management.
Oncology
Premiere Oncology is located across the street from St. John's Health Center and the John Wayne Cancer Center in Santa Monica, a 30-minute drive from Los Angeles International Airport. Our state of the art facility with views of the Pacific Ocean provides comprehensive cancer treatment. Our center has its own research laboratory and an investigational pharmacy with secure drug storage, fume hoods, high speed centrifuges, -20F, -30F, and -80F freezers, private study monitor areas, computer internet access, patient library and research patient waiting room designed to ease patient participation in research studies.
Marilyn Mulay, MSN, NP-C, OCN
Director Clinical Research Unit
Premiere Oncology
2020 Santa Monica Blvd., Suite 600
Santa Monica, CA 90404
USA
310-633-8400
310-633-8419 (fax)
mmulay@premiereoncology.com
www.premiereoncology.com
- A Phase 1 Study of Bavituximab in Patients with Solid Tumors
- A Phase 1 Study of S-1 Administered in Combination with Taxotere
- A Phase 2 Study of ARQ 197 in Patients with Microphthalmia Transciption Factor Associated Tumors
- A Phase 2 Study of the Vascular Disrupting Agent NPI-2358 in Combination with Docetaxel in Patients with Advanced Non-Small Lung Cancer
- A Phase I Dose Finding Study of TRC105 in Patients with Advanced or Metastatic Solid Cancer
- A Phase I Dose-Escalation Study of SCH900776 as Monotherapy and in Combination with Gemcitabine in Subjects with Advanced Solid Tumors or Lymphoma
- A Phase I Study of AMG 479 in Combination with either Nexavar or Erlotinib
- A Phase I Study of ARQ 197 in Combination with Tarceva in Patients with Advanced Solid Tumors
- A Phase I Study of Asonep in Subjects with Refractory Advanced Solid Tumors
- A Phase I Study of BIIB015 in Patients with Cripto-Positive Solid Tumors
- A Phase I Study of BIIB021 Administered Once or Twice Daily to Subjects with Advanced Solid Tumors
- A Phase I Study of CP751,871 + Sutent in Patients with Advanced Solid Tumors
- A Phase I Study of IPI-493 in Patients with Advanced Malignancies
- A Phase I Study of MP470 in Combination with Standard of Care Chemotherapy Regimens
- A Phase I Study of Picoplatin in Subjects with Advanced Non-Hematological Malignancies with Emphasis on Cardiac Repolarization
- A Phase I Study of Single Agent LY2584702 in Patients with Advanced or Metastatic Cancer
- A Phase I Study of SSR244738 (TED5799) in Patients with Refractory Solid Tumors
- A Phase I Study of the HSP90 Inhibitor STA-9090 in Patients with Solid Tumors
- A Phase I Study of TRC102 in Combination with Alimta in Patients with Advanced Solid Tumors
- A Phase I Study of XL518 in Subjects with Advanced Solid Tumors
- A Phase I Trial of CVX-060, an Anti-Angiogenic COVX-BODY in Patients with Advanced Solid Tumors
- A Study Evaluating the Pharmacokinetics of S-1 in patients with impaired renal function
Updated: 2/6/2009