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Keck Medical Center of USC
Phase IB Multi-Center, Cohort Dose Escalation Trial to Determine the Safety, Tolerance and Preliminary Anti-Neoplastic Activity of Gemcitabine Administered in Combination with Continuous Intravenous Doses of PRI-724, a CBP/ß-Catenin Inhibitor, to Patients with Advanced or Metastatic Pancreatic Adenocarcinoma Eligible for Second-Line Therapy After Failing First-Line Therapy with FOLFIRINOX (or FOLFOX).
Closed to Accrual with Ongoing Follow-up
Defintions of terms and FAQ about clinical trials.
Heinz Josef Lenz, M.D.
Other Trial Staff:
Ramona Lujan, R.N., Raluca Agafitei, Coordinator, Arthur Alvarez, D.M., Arthur Alvarez, D.M., Judy Lam-Tran, D.M.
to see study documents.
Click here to see trial eligibility criteria and further details at ClinicalTrials.gov
For further information on a study, please contact the Clinical Investigation Support Office at (323) 865-0451, or
To schedule a consultation with the hospital, please call our New Patient Referrals Office at (323) 865-3111.