Rebecca Arend Profile | University of ...

Dr. Rebecca C. Arend

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University of Alabama at Birmingham Cancer Center

Studies Ovarian Cancer
Studies Cancer
18 reported clinical trials
36 drugs studied

Area of expertise

1Ovarian Cancer
Rebecca C. Arend has run 9 trials for Ovarian Cancer. Some of their research focus areas include:
Stage IV
KRAS positive
NRAS positive
2Cancer
Rebecca C. Arend has run 6 trials for Cancer. Some of their research focus areas include:
KRAS positive
Stage IV
BRAF positive

Affiliated Hospitals

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University Of Alabama At Birmingham Cancer Center
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University Of Alabama At Birmingham

Clinical Trials Rebecca C. Arend is currently running

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Carboplatin + Mirvetuximab

for Ovarian Cancer

The proposed study design is a single arm Phase II trial to document the feasibility of carboplatin-mirvetuximab - in patients with advanced-stage EOC. Patients with biopsy confirmed, newly diagnosed, advanced-stage serous EOC deemed appropriate for NACT will have their tumors evaluated for FRα receptor over-expression via a centralized immunohistochemical assay (IHC) and identified as appropriate for study participation if IHC staining is PS2+ in \>75% of cells (40% of all serous patients). Eligible patients will receive NACT with one cycle of carboplatin, followed by mirvetuximab + carboplatin (if FRα +) every 21 days for three cycles prior to interval cytoreductive surgery (iCRS). A total of 70 will be included in the study. Following completion of 4 cycles total of NACT and after allowing for appropriate recovery of cycle # 4, patients eligible for surgery, will undergo an iCRS. Patients will then complete 3 more cycles of mirvetuximab + carboplatin for a total of 7 intended cycles of treatment. It is up to the treating physician if they want to add bevacizumab to the last 2 cycles or use any type of maintenance therapy. The decision to add bevacizumab or use maintenance therapy does not need to be made upfront. Patients will sign a screening consent form prior to tissue biopsy. If a patient is found to be FRα negative, their treating physician can select the treatment they deem appropriate and the patient will be declared a screen failure. Patients with BRCA mutations are not excluded from this trial and are allowed to receive standard of care maintenance therapy including bevacizumab and/or PARP inhibitors.
Recruiting1 award Phase 29 criteria
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Selumetinib + Olaparib

for Ovarian and Endometrial Cancer

This phase II ComboMATCH treatment trial compares selumetinib plus olaparib to selumetinib alone in women with endometrial or ovarian (fallopian tube and primary peritoneal) cancer that has come back (recurrent) or that remains despite treatment (persistent) and harbors a mutation in the RAS pathway. Selumetinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Olaparib is an inhibitor of PARP, an enzyme that helps repair deoxyribonucleic acid (DNA) when it becomes damaged. Blocking PARP may help keep tumor cells from repairing their damaged DNA, causing them to die. PARP inhibitors are a type of targeted therapy. The addition of olaparib to selumetinib could increase the percentage of tumors that shrink as well as lengthen the time that the tumors remain stable (without progression) as compared to selumetinib alone.
Recruiting1 award Phase 2

More about Rebecca C. Arend

Clinical Trial Related2 years of experience running clinical trials · Led 18 trials as a Principal Investigator · 9 Active Clinical Trials
Treatments Rebecca C. Arend has experience with
  • Paclitaxel
  • Olaparib
  • Binimetinib
  • Palbociclib
  • Ipatasertib
  • Selumetinib Sulfate

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