Ms. Campbell is the Chief Advanced Practice Provider. Her administrative responsibilities include oversight and standardization of recruitment/retention, professional development and engagement, quality and safety, education and research activities for Advanced Practice Providers (APPs) and Licensed Independent Practitioners (LIPs). This broad oversight includes Nurse Practitioners, Physician Assistants, CRNAs and Psychologists. Ms.
Ms. Floyd started her nursing career in 1981 graduating with a diploma in nursing and immediately transitioned into critical care. Years at the bedside and desire to grow both in skill and knowledge resulted in further pursuit of career goals including a BSN and later a Master of Science in Nursing with an Emphasis in Nursing Education (MSN-Ed) degree.
Dr. Devine is responsible for professional nursing practice across the continuum of care to ensure safety, service, and quality outcomes for Cooper University Health Care's diverse patient population. In addition, she has administrative and operational leadership responsibility for Nursing and Patient Care Services. As SVP/CNE, Dr. Devine continues to advance nursing practice by engaging nurses in re-defining a professional practice model and shared governance structure that are grounded in theoretical tenets which align to organizational mission, vision, and values.
Short Title: M20-621
The purpose of this study is to assess the change in disease activity of epcoritamab when combined with intravenous and oral rituximab, cyclophosphamide, doxorubicin hydrochloride, vincristine, and prednisone (R-CHOP) or R-CHOP in adult participants globally with diffuse large b-cell lymphoma (DLBCL). Change in disease activity will be assessed.
Epcoritamab is an investigational drug being developed for the treatment of DLBCL. Study doctors put the participants in groups called treatment arms. Participants will receive epcoritamab combined with R-CHOP, followed by epcoritamab or R-CHOP followed by rituximab will be explored.
In the Arm 1, participants will receive subcutaneous epcoritamab combined with intravenous and oral R-CHOP followed by subcutaneous epcoritamab in 21-day cycles. In the Arm 2, participants will receive intravenous and oral R-CHOP followed by intravenous rituximab in 21-day cycles.
Study Number:
M20-621
Study Status:
Enrolling
Treatment Agent:
Epcoritamab, Cyclophosphamide, Rituximab, Vincristine, Doxorubicin, Prednisone
National Clinical Trial Identified Number: NCT05578976
Disease:
Study Phase:
III
researchcancer@cooperhealth.edu
A Phase 3, Randomized, Open-Label Study to Evaluate Safety and Efficacy of Epcoritamab in Combination With R-CHOP Compared to R-CHOP in Subjects With Newly Diagnosed Diffuse Large B-Cell Lymphoma (DLBCL)
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Short Title: Phoenix
To learn if cemiplimab can help to control dMMR colon cancer.
Study Number:
2023-0228
Study Status:
Enrolling
Treatment Agent:
Cemiplimab
National Clinical Trial Identified Number: NCT05961709
Disease:
Study Phase:
II
researchcancer@cooperhealth.edu
Phase II trial of cemiplimab for the non-operative management of localized dMMR colon cancer
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Short Title: Exceptional Responders
This clinical trial studies eliminating surgery and how well radiation therapy after systemic therapy works in treating patients with HER2 positive or triple negative breast cancer when image-guided biopsy shows no residual cancer. Patients then receive standard breast radiotherapy.
Study Number:
2016-0046
Study Status:
Enrolling
Treatment Agent:
Radiation, Surgery
National Clinical Trial Identified Number: NCT02945579
Disease:
Study Phase:
Not applicable
researchcancer@cooperhealth.edu
Multicenter trial for eliminating breast cancer surgery or radiotherapy in exceptional responders to neoadjuvant systemic therapy
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Short Title: EVoPAR - Prostate 01
The intention of the study is to demonstrate superiority of Saruparib (AZD5305) + physician's choice NHA relative to placebo + physician's choice NHA by assessment of radiographic progression-free survival (rPFS) in participants with mCSPC.
Study Number:
AZD5305 - D9723C00001
Study Status:
Enrolling
Treatment Agent:
Saruparib, Abiraterone Acetate, Darolutamide, Enzalutamide
National Clinical Trial Identified Number: NCT06120491
Disease:
Study Phase:
III
researchcancer@cooperhealth.edu
A Randomized, 2-cohort, Double-blind, Placebo-controlled, Phase III Study of AZD5305 in Combination with Physician’s Choice New Hormonal Agents in Patients with HRRm and non-HRRm Metastatic Castration-Sensitive Prostate Cancer (EvoPAR-Prostate01)
Index Extra:
prostate
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Short Title: CompassHER2
This phase III trial studies how well trastuzumab emtansine (T-DM1) and tucatinib work in preventing breast cancer from coming back (relapsing) in patients with high risk, HER2 positive breast cancer. T-DM1 is a monoclonal antibody, called trastuzumab, linked to a chemotherapy drug, called DM1. Trastuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as HER2 receptors, and delivers DM1 to kill them. Tucatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving T-DM1 and tucatinib may work better in preventing breast cancer from relapsing in patients with HER2 positive breast cancer compared to T-DM1 alone.
Study Number:
A011801
Study Status:
Enrolling
Treatment Agent:
Trastuzumab emtansine, Tucatinib
National Clinical Trial Identified Number: NCT04457596
Disease:
Study Phase:
III
ResearchCancer@CooperHealth.edu
The COMPASSHER2 Trials (Comprehensive Use of Pathologic Response Assessment to Optimize Therapy in Her2-Positive Breast Cancer): Compassher2 Residual Disease (Rd), a Double-Blinded, Phase III Randomized Trial of T-Dm1 and Placebo Compared with T-Dm1 and Tucatinib
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Short Title: DIRECT
This phase II trial tests how well an imaging procedure called fludeoxyglucose F-18 (FDG) positron emission tomography/computed tomography (PET/CT) works in predicting response to standard of care chemotherapy prior to surgery in patients with HER2-positive stage IIa-IIIc breast cancer. FDG is a radioactive tracer that is given in a vein before PET/CT imaging and helps to identify areas of active cancer. PET and CT are imaging techniques that make detailed, computerized pictures of areas inside the body. The use of FDG-PET/CT may help doctors better decide if a patient needs more or less treatment before surgery in order to get the best response. This study evaluates whether FDG-PET/CT is useful in predicting a patient's response to standard of care chemotherapy.
Study Number:
EA1211
Study Status:
Enrolling
Treatment Agent:
Chemotherapy
National Clinical Trial Identified Number: NCT05710328
Disease:
Study Phase:
II
researchcancer@cooperhealth.edu
Interim FDG-PET/CT for PreDIcting REsponse of HER2+ Breast Cancer to Neoadjuvant Therapy
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Short Title: TROPION Breast 04
This is a Phase III, 2-arm, randomized, open-label, multicenter, global study assessing the efficacy and safety of neoadjuvant Dato-DXd plus durvalumab followed by adjuvant durvalumab with or without chemotherapy compared with neoadjuvant pembrolizumab plus chemotherapy followed by adjuvant pembrolizumab with or without chemotherapy in participants with previously untreated TNBC or hormone receptor-low/HER2-negative breast cancer.
Study Number:
D926QC00001
Study Status:
Enrolling
Treatment Agent:
Dato-DXd, Durvalumab, Pembrolizumab, Doxorubicin, Epirubicin, Cyclophosphamide, Paclitaxel, Carboplatin, Capecitabine, Olaparib
National Clinical Trial Identified Number: NCT06112379
Disease:
Study Phase:
III
researchcancer@cooperhealth.edu
A Phase III, Open-label, Randomized Study of Neoadjuvant Datopotamab Deruxtecan (Dato-DXd) Plus Durvalumab Followed by Adjuvant Durvalumab With or Without Chemotherapy Versus Neoadjuvant Pembrolizumab Plus Chemotherapy Followed by Adjuvant Pembrolizumab With or Without Chemotherapy for the Treatment of Adult Patients With Previously Untreated Triple-Negative or Hormone Receptor-low/HER2-negative Breast Cancer
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