Dr. Elise F. Nassif

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M D Anderson Cancer Center

Studies Soft Tissue Sarcoma
Studies Leiomyosarcoma
4 reported clinical trials
7 drugs studied

Area of expertise

1

Soft Tissue Sarcoma

Elise F. Nassif has run 4 trials for Soft Tissue Sarcoma. Some of their research focus areas include:

Stage IV
TSC2 positive
TSC1 positive
2

Leiomyosarcoma

Elise F. Nassif has run 4 trials for Leiomyosarcoma. Some of their research focus areas include:

Stage IV
TSC2 positive
TSC1 positive

Affiliated Hospitals

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M D Anderson Cancer Center

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University Of Texas MD Anderson Cancer Center LAO

Clinical Trials Elise F. Nassif is currently running

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Abemaciclib + Gemcitabine

for Soft Tissue Sarcoma

This phase I/II trial tests the side effects and best dose of abemaciclib when added to gemcitabine and compares the effectiveness of that treatment to the usual treatment of gemcitabine with docetaxel for the treatment of patients with soft tissue sarcoma that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic) (phase 1) or patients with leiomyosarcoma or dedifferentiated liposarcoma (phase 2). Abemaciclib is in a class of medications called kinase inhibitors. It works by blocking the action of an abnormal protein that signals tumor cells to multiply. This helps slow or stop the spread of tumor cells. Gemcitabine is a chemotherapy drug that blocks the cells from making deoxyribonucleic acid and may kill tumor cells. Docetaxel is in a class of medications called taxanes. It stops cancer cells from growing and dividing and may kill them. Giving abemaciclib with gemcitabine may be safe and effective when compared to treatment with gemcitabine and docetaxel for patients with advanced or metastatic soft tissue sarcoma or leiomyosarcoma or dedifferentiated liposarcoma.

Recruiting

1 award

Phase 1 & 2

5 criteria

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Low-Dose Chemotherapy + Anti-Cancer Drug

for Sarcoma

This phase I trial tests the safety, side effects, and best dose of combination therapy with liposomal doxorubicin and peposertib in treating patients with sarcoma that has spread from where it first started, to other places in the body (metastatic), or cannot be removed by surgery (unresectable) and for which no known cure is available (advanced). Doxorubicin is in a class of medications called anthracyclines. Doxorubicin damages the cell's deoxyribonucleic acid (DNA) and may kill cancer cells. It also blocks a certain enzyme needed for cell division and DNA repair. Liposomal doxorubicin is a form of the anticancer drug doxorubicin that is contained inside very tiny, fat-like particles. Liposomal doxorubicin may have fewer side effects and work better than other forms of the drug. Peposertib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It may also enhance the activity of chemo- and radiotherapy. There is some pre-clinical evidence in animal models that combining peposertib with liposomal doxorubicin can shrink or stabilize certain types of cancer for longer than either drug alone, but it is not known if this will happen in people. Combination therapy with liposomal doxorubicin and peposertib may be effective in treating patients with advanced sarcoma.

Recruiting

1 award

Phase 1

More about Elise F. Nassif

Clinical Trial Related

2 years of experience running clinical trials · Led 4 trials as a Principal Investigator · 2 Active Clinical Trials

Treatments Elise F. Nassif has experience with

  • Gemcitabine
  • Nab-Sirolimus
  • Cabozantinib
  • Ipilimumab, Nivolumab
  • Pegylated Liposomal Doxorubicin Hydrochloride
  • Peposertib

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