James Dugan, MD | Provider Profile ...

Dr. James Dugan

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Novant Health

Studies Acute Myelogenous Leukemia
Studies Acute Myeloid Leukemia
6 reported clinical trials
7 drugs studied

Area of expertise

1

Acute Myelogenous Leukemia

James Dugan has run 4 trials for Acute Myelogenous Leukemia. Some of their research focus areas include:

SF3B1 positive
U2AF1 positive
FLT3 positive
2

Acute Myeloid Leukemia

James Dugan has run 4 trials for Acute Myeloid Leukemia. Some of their research focus areas include:

SF3B1 positive
U2AF1 positive
FLT3 positive

Affiliated Hospitals

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Novant Health

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Novant Health Hematology - Forsyth

Clinical Trials James Dugan is currently running

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DFP-10917

for Acute Myeloid Leukemia

Phase III, multicenter, randomized study with two arms (1:1 ratio) enrolling patients with AML relapsed/refractory after 2, 3, or 4 prior induction regimens: Experimental arm: DFP-10917 14-day continuous intravenous (IV) infusion at a dose of 6 mg/m²/day followed by a 14-day resting period per 28-day cycles. Control arm: Non-Intensive Reinduction (LoDAC, Azacitidine, Decitabine, Venetoclax Combination Regimens) or Intensive Reinduction (High and Intermediate Dose Cytarabine Regimens), depending on the patient's prior induction treatment.

Recruiting

2 awards

Phase 3

4 criteria

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Emavusertib (+ Venetoclax)

for Acute Myeloid Leukemia

This is a multicenter, open-label, Phase 1/2a dose escalation and expansion study of orally administered emavusertib (CA-4948) monotherapy in adult patients with AML or higher- risk Myelodysplastic Syndrome (hrMDS). Patients enrolling in the Phase 1 dose escalation of the study must meet one of the following criteria prior to consenting to the study: * Relapse/refractory (R/R) AML with FMS-like tyrosine kinase-3 (FLT3) mutations who have been previously treated with a FLT3 inhibitor * R/R AML with spliceosome mutations of splicing factor 3B subunit 1 (SF3B1) or U2AF1 * R/R hrMDS with spliceosome mutations of SF3B1 or U2 small nuclear RNA auxiliary factor 1 (U2AF1) * Number of pretreatments: 1 or 2 The Phase 2a Dose Expansion will be in 3 Cohorts of patients: 1. R/R AML with FLT3 mutations who have been previously treated with a FLT3 inhibitor; 2. R/R AML with spliceosome mutations of SF3B1 or U2AF1; and 3. R/R hrMDS (Revised International Prognostic Scoring System \[IPSS-R\] score \> 3.5) with spliceosome mutations of SF3B1 or U2AF1. All patients above have had ≤ 2 lines of prior systemic anticancer treatment. In previous versions of this protocol there was a Phase 1b portion of the study, in which patients with AML or hrMDS received CA-4948 in combination with venetoclax. This part of the study is no longer open for enrollment.

Recruiting

1 award

Phase 1 & 2

9 criteria

More about James Dugan

Clinical Trial Related

4 years of experience running clinical trials · Led 6 trials as a Principal Investigator · 2 Active Clinical Trials

Treatments James Dugan has experience with

  • Azacitidine
  • Venetoclax
  • Tamibarotene
  • CA-4948
  • Asciminib
  • DFP-10917

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