Susanna Ulahannan, MD,MMEd | OU Health

Dr. Susanna Ulahannan, MD

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University of Oklahoma Health Sciences Center

Studies Colorectal Cancer
Studies Solid Tumors
24 reported clinical trials
45 drugs studied

Area of expertise

1

Colorectal Cancer

Susanna Ulahannan, MD has run 10 trials for Colorectal Cancer. Some of their research focus areas include:

Stage IV
Stage III
dMMR positive
2

Solid Tumors

Susanna Ulahannan, MD has run 9 trials for Solid Tumors. Some of their research focus areas include:

Stage IV
Stage III
KRAS positive

Affiliated Hospitals

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University Of Oklahoma Health Sciences Center

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Stephenson Cancer Center

Clinical Trials Susanna Ulahannan, MD is currently running

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TTI-101 Combination Therapy

for Liver Cancer

The primary objectives of Cohort A Phase 1b and exploratory expansion are to evaluate the safety and tolerability of TTI-101 orally administered as a single agent to participants with locally advanced or metastatic, and unresectable Hepatocellular Carcinoma (HCC) and to determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of TTI-101 as a single agent. The primary objectives of Cohort A Phase 2 are to evaluate the safety and tolerability of TTI-101 orally administered as a single agent at the RP2D to participants with locally advanced or metastatic, and unresectable HCC and to assess the preliminary efficacy of TTI-101 as a single agent in participants with locally advanced or metastatic, and unresectable HCC. The secondary objectives of Cohort A Phase 2 are to assess response, progression, survival, and pharmacokinetics. The primary objectives of Cohorts B and C Phase 1b are to evaluate the safety and tolerability of TTI-101 orally administered in combination with pembrolizumab therapy (Cohort B) and in combination with atezolizumab and bevacizumab therapy (Cohort C) to participants with locally advanced or metastatic, or unresectable HCC and to determine the MTD and/or RP2D of TTI-101 when used in combination with pembrolizumab therapy (Cohort B) and in combination with atezolizumab and bevacizumab therapy (Cohort C). The primary objectives of Cohorts B and C Phase 2 are to evaluate the safety and tolerability of TTI-101 orally administered in combination with pembrolizumab therapy (Cohort B) and in combination with atezolizumab and bevacizumab therapy (Cohort C) at the RP2D to participants with locally advanced or metastatic, and unresectable HCC and to assess the preliminary efficacy of TTI-101 in combination with pembrolizumab therapy (Cohort B) and in combination with atezolizumab and bevacizumab therapy (Cohort C) to participants with locally advanced or metastatic, and unresectable HCC. The secondary objectives of Cohorts B and C Phase 2 are to assess response, progression, survival, and pharmacokinetics.

Recruiting

2 awards

Phase 1 & 2

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TOS-358

for Cancer

This trial tests TOS-358, a new drug for adults with specific cancers that have a genetic mutation. It aims to find the safest dose and see how well patients tolerate it. The drug works by blocking a gene that helps cancer cells grow.

Recruiting

1 award

Phase 1

More about Susanna Ulahannan, MD

Clinical Trial Related

7 years of experience running clinical trials · Led 24 trials as a Principal Investigator · 4 Active Clinical Trials

Treatments Susanna Ulahannan, MD has experience with

  • Nivolumab
  • Pembrolizumab
  • Atezolizumab
  • Cetuximab
  • ZEN003694
  • TPST-1495

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