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Duke Comprehensive Cancer Center

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Durham, North Carolina 27705

Global Leader in Brain Tumor

Global Leader in Solid Tumors

Conducts research for Breast Cancer

Conducts research for Lung Cancer

Conducts research for Cancer

625 reported clinical trials

36 medical researchers

Photo of Duke Comprehensive Cancer Center in DurhamPhoto of Duke Comprehensive Cancer Center in DurhamPhoto of Duke Comprehensive Cancer Center in Durham

Summary

Duke Comprehensive Cancer Center is a medical facility located in Durham, North Carolina. This center is recognized for care of Brain Tumor, Solid Tumors, Breast Cancer, Lung Cancer, Cancer and other specialties. Duke Comprehensive Cancer Center is involved with conducting 625 clinical trials across 402 conditions. There are 36 research doctors associated with this hospital, such as Angeles A. Secord, Harry P. Erba, Jeffrey M. Clarke, and Richard Riedel, MD.

Area of expertise

1

Brain Tumor

Global Leader

Duke Comprehensive Cancer Center has run 95 trials for Brain Tumor. Some of their research focus areas include:

Stage IV
HER2 positive
Stage III
2

Solid Tumors

Global Leader

Duke Comprehensive Cancer Center has run 81 trials for Solid Tumors. Some of their research focus areas include:

Stage IV
Stage III
HER2 positive

Top PIs

Clinical Trials running at Duke Comprehensive Cancer Center

Ovarian Cancer

Breast Cancer

Cancer

Lung Cancer

Prostate Cancer

Solid Tumors

Colorectal Cancer

Fallopian Tube Cancer

Pancreatic Cancer

Brain Tumor

Image of trial facility.

Mirvetuximab + Bevacizumab

for Ovarian Cancer

GLORIOSA is a Phase 3 multicenter, open label study designed to evaluate the safety and efficacy of mirvetuximab Soravtansine + Bevacizumab as maintenance therapy in participants with platinum-sensitive ovarian, primary peritoneal or fallopian tube cancers with high folate receptor-alpha (FRα) expression.

Recruiting

2 awards

Phase 3

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Heated Chemotherapy + Niraparib

for Ovarian Cancer

Patients will be registered prior to, during or at the completion of neoadjuvant chemotherapy given per standard institutional guidelines +/- bevacizumab on Day 1 every 21 days for 3-4 cycles. Registered patients who progress during neoadjuvant chemotherapy will not be eligible for iCRS and will be removed from the study. Following completion of neoadjuvant chemotherapy, interval cytoreductive surgery (iCRS) will be performed in the usual fashion in both arms. Patients will be randomized at the time of iCRS (iCRS must achieve no gross residual disease or no disease \>1.0 cm in largest diameter) to receive HIPEC or no HIPEC. Patients randomized to HIPEC Arm will receive a single dose of cisplatin (100mg/m2 IP over 90 minutes at 42 C) as HIPEC. After postoperative recovery patients will receive standard post-operative platinum-based combination chemotherapy. Patients randomized to surgery only (No HIPEC Arm) will receive postoperative standard chemotherapy after recovery from surgery. Both groups will receive an additional 2-3 cycles of platinum-based combination chemotherapy per standard institutional guidelines +/- bevacizumab for a maximum total of 6 cycles of chemotherapy (neoadjuvant plus post-operative cycles) followed by niraparib individualized dosing +/- bevacizumab until progression or 36 months (if no evidence of disease).

Recruiting

2 awards

Phase 3

Image of trial facility.

Rina-S

for Ovarian Cancer

This phase 3 study will be conducted in different countries all over the world. The purpose of this study is to compare how well Rina-S works against platinum-resistant ovarian cancer compared to chemotherapy drugs that are already approved and used for platinum-resistant ovarian cancer. Treatment in this study could be Rina-S or it could be 1 of 4 indicated chemotherapy agents that are considered standard medical care. There is an equal (50:50) chance of getting Rina-S or an approved chemotherapy agent as treatment in this study. No one will know what treatment they are assigned to until the first dose. All participants will receive active drug; no one will be given placebo.

Recruiting

2 awards

Phase 3

4 criteria

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