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Completed

NCT Number: NCT01647828

A Phase 1b/2 Study of OMP-59R5 (Tarextumab) in Combination With Nab-Paclitaxel and Gemcitabine in Subjects With Previously Untreated Stage IV Pancreatic Cancer

The study consists of a Phase1b lead-in portion to determine the maximum tolerated dose (MTD) of OMP-59R5 in combination with nab-paclitaxel and gemcitabine followed by a Phase 2, multicenter, randomized, placebo-controlled portion to evaluate the efficacy and safety of OMP-59R5 in combination with nab-paclitaxel and gemcitabine in subjects with previously untreated stage IV pancreatic cancer.

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Western Regional Medical Center, Inc., Goodyear, Arizona, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Subjects must meet all of the following major inclusion criteria to be eligible for the study:

  • 18 years of age or older
  • Histologically or cytologically documented stage IV ductal adenocarcinoma of the pancreas.
  • Performance Status (ECOG) 0 or 1
  • FFPE tumor tissue from metastatic site(s
  • Adequate organ function
  • Written consent on an IRB/IEC-approved Informed Consent Form prior to any study-specific evaluation.
  • For women of child-bearing potential, negative serum pregnancy test at screening and use of physician-approved method of birth control from 30 days prior to the first study drug administration to 30 days following the last study drug administration.
  • Male subjects must be surgically sterile or must agree to use physician-approved contraception from 30 days prior to the first study drug administration to 30 days following the last study drug administration.

Exclusion criteria

Subjects who meet any of the following major exclusion criteria will not be eligible for participation in the study:

  • Neuroendocrine tumors (i.e., carcinoid, islet cell cancer) of the pancreas.
  • Known brain metastases.
  • Prior therapy, including systemic therapy, surgical resection or radiation for newly diagnosed stage IV pancreatic cancer.
  • Presence of any serious or unstable concomitant systemic disorder incompatible with the clinical study (e.g., substance abuse, uncontrolled intercurrent illness including active infection, arterial thrombosis, symptomatic pulmonary embolism).
  • Any disorder that would significantly compromise protocol compliance.
  • Prior non-pancreatic malignancy treated with chemotherapy. Prior malignancies treated with surgery and/or radiotherapy alone must be in remission ≥3 years. The following prior malignancies are allowable irrespective of when they occurred: in situ carcinoma of the cervix, in situ ductal breast cancer, low-grade local bladder cancer, and nonmelanotic skin cancer.
  • Known human immunodeficiency virus (HIV) infection.
  • Females who are pregnant or breastfeeding.

Treatment and study plan

OMP-59R5

Drug

OMP-59R5 administered intravenously

Gemcitabine

Drug

administered intravenously

Placebo

Drug

administered IV

Nab-paclitaxel

Drug

administered intravenously

Other names: Abraxane

Primary outcomes

  1. Phase Ib: Number of Participants With Dose-limiting Toxicities (DLT)

    Time frame: Up to 1 year in absence of unacceptable toxicity or disease progression.

    Number of participants with dose-limiting toxicities when administered OMP-59R5 every of other week (Days 1 and 15) in combination with nab-paclitaxel (Nab-P) 125 mg/m2 and gemcitabine (Gem) 1000 mg/m2 on Days 1, 8, and 15 of every 28-day cycle in subjects with previously untreated stage IV pancreatic cancer. In the event that no DLTs are observed, maximum tested dose would be considered the Maximum Tolerated Dose (MTD).

  2. Phase 2: Overall Survival (ITT Population)

    Time frame: Up to 1 year in absence of unacceptable toxicity or disease progression.

    To determine the clinical benefit, as measured by overall survival (OS) ofthe addition of OMP-59R5 to nab-paclitaxel and gemcitabine in all subjects who are receiving first-line therapy for stage IV pancreatic cancer.

  3. Phase 2: Median OS by Notch 3 Percentile (ITT Population)

    Time frame: Up to 1 year in absence of unacceptable toxicity or disease progression.

    To determine the clinical benefit, as measured by OS of the addition of OMP-59R5 to Nab-P+Gem across the 4 subject subsets: subjects with Notch3 ≥ 25th percentile, subjects with Notch3 ≥ 50th percentile, subjects with Notch3 ≥ 75th percentile and all subjects receiving first-line therapy for stage IV pancreatic cancer with Notch3 high expression level.

Sponsors and collaborators

Lead sponsor

OncoMed Pharmaceuticals, Inc.

Industry

Registry information

Official study title

A Phase 1b/2 Study of OMP-59R5 in Combination With Nab-Paclitaxel and Gemcitabine in Subjects With Previously Untreated Stage IV Pancreatic Cancer

Acronym: ALPINE

Important dates

Study start
2012
Primary completion
2016
Study completion
2016
First posted
Jul 24, 2012
Registry last updated
Feb 15, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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