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
35 drugs studied

Area of expertise

1

Ovarian Cancer

Rebecca C. Arend has run 8 trials for Ovarian Cancer. Some of their research focus areas include:

KRAS positive
Stage IV
NRAS positive
2

Cancer

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.

Recruiting

1 award

Phase 2

9 criteria

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pBI-11 Vaccine

for Human Papillomavirus Infection

This research is being done to test the safety and feasibility of an investigational DNA vaccine called pBI-11 and to find out what effects, if any, it has on women with persistent human papillomavirus 16 (HPV16+) and/or human papillomavirus (HPV18+) cervical infection. The DNA vaccine is designed to promote an immune response to treat disease caused by HPV types 16 and 18, viruses that can cause cervical cancer. The pBI-11 DNA vaccine or a placebo will be administered intramuscularly using the TriGridTM Delivery System.

Recruiting

0 awards

Phase 2

4 criteria

More about Rebecca C. Arend

Clinical Trial Related

3 years of experience running clinical trials · Led 18 trials as a Principal Investigator · 5 Active Clinical Trials

Treatments Rebecca C. Arend has experience with

  • Paclitaxel
  • Binimetinib
  • Olaparib
  • Palbociclib
  • Ipatasertib
  • Selumetinib Sulfate

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