Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 1Phase 2 Interventional

A Study Evaluating IPI-926 in Combination With Gemcitabine in Patients With Metastatic Pancreatic Cancer

ClinicalTrials.gov ID: NCT01130142

Public ClinicalTrials.gov record NCT01130142. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 1:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b/2 Study Evaluating IPI-926 in Combination With Gemcitabine in Patients With Metastatic Pancreatic Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Study IPI-926-03 is a Phase 1b/2 clinical trial to evaluate IPI 926 in combination with gemcitabine in patients with previously untreated metastatic pancreatic cancer. Phase 1b is designed as a dose escalation study. Once the maximum tolerated dose of IPI-926 in combination with gemcitabine is established in the Phase 1b portion of the study, the Phase 2 portion will commence. Phase 2 is designed as a randomized, double-blind (investigator/patient), placebo-controlled study. There is no cross-over option for patients in either arm of the Phase 2 (i.e., there is no option for patients receiving placebo to cross-over to IPI-926).

Study identification

NCT ID
NCT01130142
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Infinity Pharmaceuticals, Inc.
Industry
Enrollment
122 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2010
Primary completion
Apr 30, 2012
Completion
Apr 30, 2012
Last update posted
Mar 5, 2017

2010 – 2012

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
24
Facility City State ZIP Site status
Arizona Clinical Research Center Tucson Arizona 85745
University of California San Diego Medical Center San Diego California
University of California San Francisco San Francisco California
Kaiser Permanente Vallejo California 94503
University of Colorado Cancer Center Aurora Colorado 80045
H. Lee Moffitt Cancer Center and Research Institute Tampa Florida 33612
Kansas City Cancer Center Overland Park Kansas 66210
Norton Health Care Louisville Kentucky 40220
Dana-Farber Cancer Institute Boston Massachusetts 02115
West Michigan Cancer Center Kalamazoo Michigan 49007
Hackensack University Medical Center Hackensack New Jersey
Columbia University Medical Center New York New York 10032
Weill Cornell Medical Center New York New York 10065
University of Rochester Rochester New York 14604
Willamette Valley Cancer Institute and Research Center Eugene Oregon 97401
Providence Portland Medical Center Portland Oregon 97213
University of Pittsburgh Medical Center Pittsburgh Pennsylvania
Rhode Island Hospital Providence Rhode Island
Institute of Translational Oncology Research Greenville South Carolina 29605
Texas Oncology- Bedford Bedford Texas
Texas Oncology, PA Dallas Texas 75246
South Texas Oncology and Hematology San Antonio Texas
Tyler Cancer Center Tyler Texas 75702
Virginia Oncology Associates Newport News Virginia 23606
Seattle Cancer Care Alliance Seattle Washington 98109

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01130142, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 5, 2017 · Synced Sep 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01130142 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →