Sudhir Manda, MD, FACP - Arizona Oncology

Dr. Sudhir Manda

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Arizona Oncology Associates

Studies Lymphoma
Studies B-Cell Lymphoma
17 reported clinical trials
40 drugs studied

About Sudhir Manda

Education:

  • Obtained MD from the University of Arizona College of Medicine, Tucson, AZ.
  • Completed Residency in Internal Medicine at the University of Arizona College of Medicine, Tucson, AZ.
  • Undertook Fellowship in Hematology/Oncology at the University of Arizona Cancer Center, Tucson, AZ.

Experience:

  • Board-certified in Internal Medicine, Hematology, and Medical Oncology.
  • Associated with Arizona Oncology Associates.

Area of expertise

1

Lymphoma

Sudhir Manda has run 5 trials for Lymphoma. Some of their research focus areas include:

metastatic
RECIST 1.1
nonsmall cell lung cancer
2

B-Cell Lymphoma

Sudhir Manda has run 4 trials for B-Cell Lymphoma. Some of their research focus areas include:

MYC positive
Bcl2 positive
Bcl6 positive

Affiliated Hospitals

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Arizona Oncology Associates

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Arizona Oncology Associates, PC - HOPE

Clinical Trials Sudhir Manda is currently running

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Tazemetostat + Lenalidomide + Rituximab

for Follicular Lymphoma

The participants of this study would have relapsed/refractory follicular lymphoma. Follicular lymphoma is a type of blood cancer. It is referred to as 'relapsed' when the disease has come back after a period of improvement after that follows a treatment regimen and 'refractory' when treatment no longer works. Stage 1 of this trial will study the safety and the level that adverse effects of each of the study drug combinations can be tolerated (known as tolerability). It is also designed to establish a recommended study drug dosage for stage 2 and 3. Stage 1 of the study is completed. Stages 2 and 3 will evaluate and compare how long participants live without their disease getting worse when receiving the study drug in combination with other drug treatment versus the placebo (dummy drug) in combination with other drug treatment.

Recruiting

1 award

Phase 3

4 criteria

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Selinexor + R-GDP

for Lymphoma

The purpose of this Phase 2/3 study is to evaluate efficacy and safety of the combination of selinexor and R-GDP (SR-GDP) in patients with RR DLBCL who are not intended to receive hematopoetic stem cell transplantation (HSCT) or chimeric antigen receptor T cell (CAR-T) therapy. This study consists of 3 arms each in Phase 2 and 3. Phase 2 portion of the study will assess the two doses of selinexor (40 milligram \[mg\] or 60 mg) in combination with R-GDP, for up to 6 cycles (21-day per cycle), followed by 60 mg selinexor single agent continuous therapy for those who have reached a partial or complete response. Phase 3 portion of the study will evaluate the selected dose of SR-GDP (identified in Phase 2) versus standard R-GDP + matching placebo, for up to 6 cycles (21-day per cycle), followed by placebo or 60 mg selinexor single agent continuous therapy for those who have reached partial or complete response.

Recruiting

0 awards

Phase 2 & 3

9 criteria

More about Sudhir Manda

Clinical Trial Related

5 years of experience running clinical trials · Led 17 trials as a Principal Investigator · 2 Active Clinical Trials

Treatments Sudhir Manda has experience with

  • Lenalidomide
  • Rituximab
  • Pembrolizumab
  • Dexamethasone
  • Gemcitabine
  • Selinexor

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