A022104
Short Title: JANUS
This phase II trial compares the effect of irinotecan versus oxaliplatin after long-course chemoradiation in patients with stage II-III rectal cancer. Combination chemotherapy drugs, such as FOLFIRINOX (fluorouracil, irinotecan, leucovorin, and oxaliplatin), FOLFOX (leucovorin, fluorouracil, oxaliplatin, and irinotecan), and CAPOX (capecitabin and oxaliplatin) work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.
Study Number:
A022104
Study Status:
Enrolling
Treatment Agent:
Capecitabine, 5-fluorouracil, Leucovorin calcium, Irinotecan, Oxaliplatin
Resources and Links
National Clinical Trial Identified Number: NCT05610163
Disease:
- Locally Advanced Rectal Carcinoma
Study Phase:
II
researchcancer@cooperhealth.edu
Article Title
A Randomized Phase II Trial Testing the Efficacy of Triplet Versus Doublet Chemotherapy to Achieve Clinical Complete Response in Patients with Locally Advanced Rectal Cancer
Index Extra:
GI, gastro, rectal
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PRAGMATICA
Short Title: PRAGMATICA
This phase III trial compares the effect of the combination of ramucirumab and pembrolizumab versus standard of care chemotherapy for the treatment of non-small cell lung cancer that is stage IV or that has come back after a period of improvement (recurrent). Ramucirumab is a monoclonal antibody that may prevent the growth of new blood vessels that tumors need to grow. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.
Study Number:
S2302
Study Status:
Enrolling
Treatment Agent:
Pembrolizumab, Ramucirumab
Resources and Links
National Clinical Trial Identified Number: NCT05633602
Disease:
- Recurrent Lung Non-Small Cell Carcinoma,
- Stage IV Lung Cancer
Study Phase:
III
researchcancer@cooperhealth.edu
Article Title
A Prospective Randomized Study of Ramucirumab Plus Pembrolizumab Versus Standard of Care for Participants Previously Treated with Immunotherapy for Stage IV or Recurrent Non-Small Cell Lung Cancer
Index Extra:
lung, thoracic
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SURVENT
Short Title: SURVENT
The trial’s primary aim is to determine if patients undergoing endoscopic eradication therapy will demonstrate less neoplastic progression and a lower incidence of esophageal adenocarcinoma compared to patients undergoing surveillance.
Study Number:
SURVENT
Study Status:
Enrolled
Treatment Agent:
Not Applicable
Resources and Links
National Clinical Trial Identified Number: NCT05753748
Disease:
- Barrett’s Esophagus with Low-grade Dysplasia,
- Esophageal Adenocarcinoma
Study Phase:
Not Applicable
researchcancer@cooperhealth.edu
Article Title
A Multicenter Randomized Controlled Trial of Surveillance vs. Endoscopic Therapy for Barrett’s Esophagus with Low-grade Dysplasia
Index Extra:
Esophageal, head and neck, Dysplasia, Barrett’s, Esophagus, gastro
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SOROCk
Short Title: SOROCk
This clinical trial studies how well two surgical procedures (bilateral salpingectomy and bilateral salpingo-oophorectomy) work in reducing the risk of ovarian cancer for individuals with BRCA1 mutations. Bilateral salpingectomy involves the surgical removal of fallopian tubes, and bilateral salpingo-oophorectomy involves the surgical removal of both the fallopian tubes and ovaries. This study may help doctors determine if the two surgical procedures are nearly the same for ovarian cancer risk reduction for women with BRCA1 mutations.
Study Number:
CC008
Study Status:
Enrolling
Treatment Agent:
Not Applicable
Resources and Links
National Clinical Trial Identified Number: NCT04251052
Disease:
- Ovarian Carcinoma
Study Phase:
Not Applicable
ResearchCancer@CooperHealth.edu
Article Title
A Non-Randomized Prospective Clinical Trial Comparing the Non-Inferiority of Salpingectomy to Salpingo-oophorectomy to Reduce the Risk of Ovarian Cancer Among BRCA1 Carriers [SOROCk]
Index Extra:
Ovarian, gyn, Gynecologic
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DECREASE
Short Title: DECREASE
This phase II trial studies how well lower-dose chemotherapy plus radiation (chemoradiation) therapy works in comparison to standard-dose chemoradiation in treating patients with early-stage anal cancer. Drugs used in chemotherapy, such as mitomycin, fluorouracil, and capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Radiation therapy uses high-energy x-rays to kill tumor cells and shrink tumors. Giving chemotherapy with radiation therapy may kill more tumor cells. This study may help doctors find out if lower-dose chemoradiation is as effective and has fewer side effects than standard-dose chemoradiation, which is the usual approach for treatment of this cancer type.
Study Number:
EA2182
Study Status:
Enrolling
Treatment Agent:
Capecitabine, Fluorouracil, Mitomycin
Resources and Links
National Clinical Trial Identified Number: NCT04166318
Disease:
- Anal Basaloid Carcinoma,
- Anal Canal Cloacogenic Carcinoma,
- Anal Canal Squamous Cell Carcinoma,
- Anal Margin Squamous Cell Carcinoma
Study Phase:
II
researchcancer@cooperhealth.edu
Article Title
A Randomized Phase II Study of De-Intensified ChemoRadiation for Early-Stage Anal Squamous Cell Carcinoma
Index Extra:
GI, Anal
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SAMURAI
Short Title: SAMURAI
This phase II trial tests whether the addition of radiation to the primary tumor, typically given with stereotactic ablative radiation therapy (SABR), in combination with standard of care immunotherapy improves outcomes in patients with renal cell cancer that is not recommended for surgery and has spread to other places in the body (metastatic).
Study Number:
GU012
Study Status:
Enrolling
Treatment Agent:
Avelumab, Axitinib, Cabozantinib, Ipilimumab, Lenvatinib, Nivolumab, Pembrolizumab
Resources and Links
National Clinical Trial Identified Number: NCT05327686
Disease:
- Metastatic Renal Cell Carcinoma,
- Unresectable Renal Cell Carcinoma
Study Phase:
II
researchcancer@cooperhealth.edu
Article Title
Randomized Phase II Stereotactic Ablative Radiation Therapy (SABR) For Metastatic Unresected Renal Cell Carcinoma (RCC) Receiving Immunotherapy
Index Extra:
GU, Renal
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TROPION- BREAST 03
Short Title: TROPION- BREAST 03
The study will investigate the efficacy and safety of Dato-DXd with or without durvalumab when compared with ICT (capecitabine and/or pembrolizumab) in participants with stage I to III TNBC who have residual invasive disease in the breast and/or axillary lymph nodes at surgical resection following neoadjuvant systemic therapy.
Study Number:
D926XC00001
Study Status:
Enrolling
Treatment Agent:
Dato-DXd, Durvalumab, Capecitabine, Pembrolizumab
Resources and Links
National Clinical Trial Identified Number: NCT05629585
Disease:
- Stage I-III Triple-negative Breast Cancer
Study Phase:
III
ResearchCancer@CooperHealth.edu
Article Title
A Phase III Open-label, Randomised Study of Datopotamab Deruxtecan (Dato-DXd) With or Without Durvalumab Versus Investigator’s Choice of Therapy in Patients With Stage I-III Triple-negative Breast Cancer Who Have Residual Invasive Disease in the Breast and/or Axillary Lymph Nodes at Surgical Resection Following Neoadjuvant Systemic Therapy
Index Extra:
breast
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