Dr. Suzanne R. Fanning, DO | Greenville ...

Dr. Suzanne R. Fanning

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Prisma Health Cancer Institute - Eastside

Studies Adult T-Cell Leukemia/Lymphoma
Studies Lymphoma
12 reported clinical trials
35 drugs studied

Area of expertise

1Adult T-Cell Leukemia/Lymphoma
Suzanne R. Fanning has run 6 trials for Adult T-Cell Leukemia/Lymphoma. Some of their research focus areas include:
BCR-ABL1 positive
FLT3 positive
13q positive
2Lymphoma
Suzanne R. Fanning has run 5 trials for Lymphoma. Some of their research focus areas include:
Stage I
13q positive
13q negative

Affiliated Hospitals

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Prisma Health Cancer Institute - Eastside
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Prisma Health Cancer Institute - Spartanburg

Clinical Trials Suzanne R. Fanning is currently running

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Venetoclax + HMA

for Acute Myeloid Leukemia

This phase II MyeloMATCH treatment trial compares the usual treatment of azacitidine and venetoclax to the combination treatment of azacitidine, venetoclax and gilteritinib in treating older and unfit patients with acute myeloid leukemia and FLT3 mutations. Azacitidine is a drug that is absorbed into DNA and leads to the activation of cancer suppressor genes, which are genes that help control cell growth. Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein needed for cancer cell survival. Gilteritinib is in a class of medications called kinase inhibitors. It works by blocking the action of a certain naturally occurring substance that may be needed to help cancer cells multiply. This study may help doctors find out if these different approaches are better than the usual approaches. To decide if they are better, the study doctors are looking to see if the study drugs lead to a higher percentage of patients achieving a deeper remission compared to the usual approach.
Recruiting1 award Phase 27 criteria
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Iberdomide

for Multiple Myeloma

This phase II trial compares iberdomide maintenance therapy to disease monitoring for improving survival in patients who have received idecabtagene vicleucel (a type of chimeric antigen receptor T-cell \[CAR-T\] therapy) for multiple myeloma. The usual approach after treatment with idecabtagene vicleucel is to monitor the multiple myeloma without giving myeloma medications. There is currently no medication approved specifically for use after idecabtagene vicleucel treatment. Upon administration, iberdomide modifies the immune system and activates immune cells called T-cells, which could enhance the effectiveness of idecabtagene vicleucel. Iberdomide may keep multiple myeloma under control for longer than the usual approach (disease monitoring) after idecabtagene vicleucel, and may help multiple myeloma patients live longer.
Recruiting1 award Phase 210 criteria

More about Suzanne R. Fanning

Clinical Trial Related2 years of experience running clinical trials · Led 12 trials as a Principal Investigator · 10 Active Clinical Trials
Treatments Suzanne R. Fanning has experience with
  • Venetoclax
  • Cytarabine
  • Azacitidine
  • Daunorubicin Hydrochloride
  • Dexamethasone
  • Cyclophosphamide

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