About Sarah Cannon Research Institute at HealthONE
Sarah Cannon Research Institute at HealthONE is determined to make a difference in our patients' lives. Through Sarah Cannon, we are a part of a network that has conducted community-based clinical trials for more than 20 years and has conducted 260+ first-in-man clinical trials to date. Sarah Cannon Research Institute has been a clinical trial leader in the majority of approved cancer therapies over the last 10 years. 
Our Integrated Care
Together, Sarah Cannon Research Institute and HealthONE offer integrated cancer services and treatment options to patients across the Rocky Mountain region. Through our partnership, we pair cutting-edge clinical cancer research with state-of-the-art technology to enhance the lives of cancer patients.
Our Philosophy
Participation in a clinical trial is the first step in fighting cancer, not the last.®
At Sarah Cannon Research Institute at HealthONE, we believe clinical trials are a source of inspiration and a catalyst for hope. Our experienced team is committed to delivering the highest quality care, personalized attention and revolutionary technology to provide patients with access to promising and innovative clinical trials in Denver. Want to learn more about HealthONE’s partnership with Sarah Cannon? Find out more below.
Clinicians
Gerald S. Falchook, MD - Director, Drug Development
Michael L. Pearlman, MD, PhD - Neuro Oncologist
Lindsay Bramwell, MSN, RN, ACNS-BC - Nurse Practitioner
Tracey Way, FNP-BC, OCN, CCRP - Nurse Practitioner
Program Manager
Kelly Mozzetta
Clinic Lead
Yesenia Mastache
Pharmacist
Peter Schlickman, Pharm.D.
Research Nurses
Markia Ward
Sonya Mihalus
Treatment Nurses
Bonnie Sumner
Sheila Lyons
Kristy Cauthen
Lindsay McFall
Medical Office Specialist
Sarah Kirk
Laboratory Technicians
Aleisha Green
Michael Nowicki
Medical Assistants
Nick Saenz
Justina Duran
Data Coordinators
Jacob Leary
Cassie Stone
Clinical Trial Specialist
Kari Koga
Contact Us: (720)-754-2610
The First Step
Sarah Cannon Research Institute at HealthONE is determined to make a difference in the lives of our patients and so many others. We currently have clinical trials actively enrolling patients. If you are interested in finding out more information related to our clinical trials, please call: (720)-754-2610.
Speak to Your Doctor
If you are interested in participating in a clinical trial, contacting your doctor is the first step. We will coordinate with your doctor directly to see if you are a good fit for the trial. If you are eligible and choose to take part in a study, you may be able to receive new, cutting-edge treatment and help to improve the lives of future cancer patients.
What to Expect
- Experienced and personalized care from esteemed physicians and renowned leaders in cancer drug development
- Innovative cancer treatment options close to home in Denver
- Support from a passionate and caring team of medical professionals
- Clear and open communication about clinical trial options
- Personalized cancer treatment strategies through genomic tumor testing
- A newly renovated facility that includes a clinic, an infusion center, an investigational pharmacy, a lab processing area and office space
Sarah Cannon Research Institute at HealthONE is part of Sarah Cannon, the Cancer Institute of HCA Healthcare. Together, Sarah Cannon and HealthONE offer integrated cancer services to communities across the greater Denver area and Rocky Mountain region, which can be accessed at the following HealthONE family of hospitals:
- The Medical Center of Aurora
- North Suburban Medical Center
- Presbyterian/St. Luke's Medical Center
- Rocky Mountain Blood and Marrow Transplant Program
- Rocky Mountain Hospital for Children
- Rose Medical Center
- Sky Ridge Medical Center
- Swedish Medical Center
Through our partnership, we pair cutting-edge research with world-class cancer services that span the entire cancer care journey from diagnosis through survivorship.
Open Trials and Patient Referrals
To view clinical cancer trials that are currently enrolling, click the link below. For more information about our current trials or for general inquiries, call us at (720)-754-2610 or email us.
Contact Us: (720)-754-2610Sarah Cannon Research Institute at HealthONE
1800 Williams Street
Suite 300
Denver, CO 80218
Open Clinical Trials
A Phase 1, First-in-Human, Safety, Dose Tolerance, Pharmacokinetics, and Pharmacodynamics Study of CPX-POM in Patients with Advanced Solid Tumors
A Phase 1 Trial of MK-4280 as Monotherapy and in Combination with Pembrolizumab in Subjects with Advanced Solid Tumors
A Pharmacodynamic Study of Oral eFT508 in Subjects With Advanced Triple Negative Breast Cancer and Hepatocellular Carcinoma
A Study of Toca 511, a Retroviral Replicating Vector, Combined With Toca FC in Patients With Solid Tumors or Lymphoma (Toca 6)
A Phase 1 Study of RGX-104, a Small Molecule LXR Agonist, in Patients with Advanced Solid Malignancies and Lymphoma with an Expansion in Select Malignancies
A Phase 2, Open-Label, Randomized, Non-comparative Study With Preliminary Dose-Finding to Evaluate eFT508 Monotherapy or eFT508 in Combination With Avelumab in Subjects With Microsatellite Stable Relapsed or Refractory Colorectal Cancer
RM 519
A Phase 1 Study to Evaluate the Potential Pharmacokinetic Interaction Between Entrectinib and Midazolam in Cancer Patients
An Open-Label, Phase 2, Parallel Arm Study to Evaluate the Safety, Tolerability, and Activity of TAK-931 Single Agent in Patients with Metastatic Pancreatic Cancer or Metastatic Colorectal Cancer
A Phase 1b/2 study to assess the safety, tolerability and efficacy of BGB-290 in combination with radiation therapy and/or temozolomide in subjects with first-line or recurrent/refractory glioblastoma
A Phase 1/2a, open-label, multicenter study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of PEN-866 in patients with advanced solid malignancies
Effects of Multiple Doses of Abemaciclib on the Pharmacokinetics of Cytochrome P450 (CYP) 1A2, CYP2C9, CYP2D6, and CYP3A Substrates (Caffeine, Warfarin, Dextromethorphan, and Midazolam) in Cancer Patients
A Phase 1 Open-label Dose Escalation Study of CGX1321 in Subjects with Advanced Solid Tumors
A Phase 1b Dose Escalation Study of the Safety and Pharmacodynamics of Brontictuzumab in Combination with Chemotherapy for Subjects with Previously Treated Metastatic Colorectal Cancer
A Phase 1, Open-Label, Dose Escalation and Dose Expansion Trial Evaluating the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Effects of Orally Administered CA-170 in Patients with Advanced Tumors and Lymphomas
Phase 1/2 Multicenter Trial of ICOS Agonist Monoclonal Antibody (mAb) JTX-2011 Alone or in Combination With Nivolumab in Adult Subjects with Advanced Refractory Solid Tumor Malignancies
A Phase II Study to Evaluate the Activity of Commercially Available Molecularly Matched Targeted Therapies in Selected Tumor Types Based on Genomic Alterations
A Phase 1 Dose Escalation and Cohort Expansion Study of TSR-022, an anti-TIM-3 Monoclonal Antibody, in Patients with Advanced Solid Tumors
A Phase 1, Two-Cohort, Open-Label, Drug- Drug Interaction Study of Entinostat and Exemestane in Postmenopausal Women with Locally Recurrent or Metastatic ER+ Breast Cancer
A Phase 1/1b Trial Investigating the CSF-1R Inhibitor LY3022855 in Combination with Durvalumab or Tremelimumab in Patients with Advanced Solid Tumors
A Phase 1/2a, dose-escalation study of FF-10502-01 for the treatment of advanced solid tumors and lymphomas
Safety, Tolerability and Pharmacokinetics of AZD1775 Plus MEDI4736 in Patients With Advanced Solid Tumours
A Phase 1-2 Dose-Escalation and Cohort-Expansion Study of Oral eFT508 in Subjects with Advanced Solid Tumors
A Phase Ib Study to Determine the Maximum Tolerated Dose (MTD) of AZD1775 Monotherapy in Patients with Locally Advanced or Metastatic Solid Tumours
A Multi-Center, Open-Label Study of Sulfatinib(HMPL-012) in Patients With Advanced Solid Tumors
A Phase I, Open-Label,Multicentre Dose Escalation Study to Assess the Safety, Tolerability, and Pharmacokinetics of AZD2811 in Patients with Advanced Solid Tumours
A Phase I Open-Label Study to Determine the Safety and Tolerability of ALRN-6924 in Patients with Advanced Solid Tumors or Lymphomas Expressing Wild-Type p53 Protein
A Phase Ib Study of AZD1775 and olaparib in Patients with Refractory Solid Tumors
A Phase 1b/2, Open-Label, Multicentre Study Assessing the Safety, Tolerability, Pharmacokinetics, and Preliminary Anti-tumour Activity of MEDI4736 in Combination With AZD9150 or AZD5069 in Patients With Advanced Solid Malignancies and Subsequently Comparing AZD9150 and AZD5069 Both as Monotherapy and in Combination With MEDI4736 as Second Line Treatment in Patients With Recurrent and/or Metastatic Squamous Cell Carcinoma of the Head and Neck
Phase Ib Study Evaluating the c-Met Inhibitor INC280 in Combination With Bevacizumab in Glioblastoma Multiforme (GBM), Metastatic Colorectal Cancer (mCRC) and Metastatic Renal Cell Carcinoma (mRCC) Patients
A Phase 1/2 Study Exploring the Safety, Tolerability, and Efficacy of INCB024360 in Combination With MEDI4736 in Subjects With Selected Advanced Solid Tumors
Phase 1, Open-Label, Dose-Escalation, Safety and Tolerability Study of INCB054329 in Subjects With Advanced Malignancies
A First-in-Human Study of Repeat Dosing With REGN2810, a Monoclonal, Fully Human Antibody to Programmed Death - 1 (PD 1), as Single Therapy and in Combination With Other Anti-Cancer Therapies in Patients With Advanced Malignancies
