Trial record 4 of 5 for:    INCB039110

Safety Study of INCB039110 in Combination With Gemcitabine and Nab-Paclitaxel in Subjects With Advanced Solid Tumors

This study is currently recruiting participants. (see Contacts and Locations)
Verified August 2013 by Incyte Corporation
Sponsor:
Information provided by (Responsible Party):
Incyte Corporation
ClinicalTrials.gov Identifier:
NCT01858883
First received: May 14, 2013
Last updated: August 23, 2013
Last verified: August 2013
  Purpose

Test the hypothesis that INCB039110 can be administered safely in combination with gemcitabine and nab-paclitaxel in subjects with advanced or metastatic cancer.


Condition Intervention Phase
Metastatic Cancer
Metastatic Pancreatic Cancer
Drug: INCB039110
Drug: Gemcitabine
Drug: nab-paclitaxel
Phase 1

Study Type: Interventional
Study Design: Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Phase 1B Study of the Safety and Tolerability of INCB039110 in Combination With Gemcitabine and Nab-Paclitaxel in Subjects With Advanced Solid Tumors

Resource links provided by NLM:


Further study details as provided by Incyte Corporation:

Primary Outcome Measures:
  • Safety and tolerability of the treatment regimen as measured by the number of participants with adverse events. [ Time Frame: Baseline and weekly for Cycle 1 and then Day 1, Week 8 and Week 15 for all subsequent cycles until the End of Treatment visit (approximately 6 months). ] [ Designated as safety issue: Yes ]
  • Identify the 'Maximum Tolerated Dose (MTD) within a defined dose range for INCB039110 in the combination regimen. [ Time Frame: Each cohort will be observed for a minimum of 28 days. ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Plasma concentration of tumor specific biomarkers and cytokines before and during treatment. [ Time Frame: Baseline up to 6 months. ] [ Designated as safety issue: No ]
  • Clinical activity as measured by the greatest decrease in tumor burden compared to baseline. [ Time Frame: Baseline and approximately every two cycles throughout the study until study completion or early termination (approximately 6 months). ] [ Designated as safety issue: No ]

Estimated Enrollment: 42
Study Start Date: June 2013
Estimated Study Completion Date: October 2014
Estimated Primary Completion Date: September 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: INCB039110, gemcitabine, nab-paclitaxel Drug: INCB039110
600QD, 400QD, and 300QD
Drug: Gemcitabine
1000 mg/m2
Other Name: Gemzar
Drug: nab-paclitaxel
125 mg/m2, 100 mg/m2
Other Name: Abraxane

Detailed Description:

Study Part 1: This is a dose optimization phase designed to find a tolerated regimen that includes the maximum tolerated dose of INCB039110 (within a defined pharmacologic range) in combination with doses of gemcitabine and nab-paclitaxel that have established safety and tolerability in subjects with advanced or metastatic solid tumors.

Study Part 2: This phase will explore the safety and clinical activity of the regimen identified in Part 1, in subjects with advanced or metastatic pancreatic cancer.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Histologically or cytologically confirmed solid tumor (Part 1) or pancreatic adenocarcinoma (Part 2)
  • ECOG performance status ≤ 1
  • Received no more than 1 prior chemotherapy regimen for advanced or metastatic disease (not including neo-adjuvant and/or adjuvant therapy)
  • There is no restriction on the number of prior non-myelosuppressive targeted therapies or hormonal agents (eg, EGFR targeted therapy for lung cancer and hormonal therapy for breast cancer or ovarian cancer); targeted and/or hormonal therapy alone will not be considered chemotherapy for the purposes of this study.
  • Adequate renal, hepatic, and bone marrow function without blood product or hematopoietic growth factor support:
  • Ability to swallow and retain oral medication

Exclusion Criteria:

  • Any known contraindications to the use of gemcitabine or nab-paclitaxel.
  • Evidence of uncontrolled brain metastases or history of uncontrolled seizures.
  • Ongoing radiation therapy and/or radiation therapy administered within 28 days of enrollment or ongoing radiotherapy-related toxicities.
  • Presence of ≥ Grade 2 neuropathy.
  • Inability to swallow food or any condition of the upper GI tract that precludes administration of oral medications.
  • Recent (≤ 3 months) history of partial or complete bowel obstruction.
  • Unwillingness to be transfused with blood components.
  • Known history of Hepatitis B or C infection or HIV infection
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01858883

Contacts
Contact: Inycte Corporation Call Center 1-855-463-3463

Locations
United States, Arizona
Recruiting
Scottsdale, Arizona, United States
United States, Arkansas
Recruiting
Fayetteville, Arkansas, United States
United States, Indiana
Recruiting
Indianapolis, Indiana, United States
United States, Pennsylvania
Recruiting
Philadelphia, Pennsylvania, United States
Sponsors and Collaborators
Incyte Corporation
Investigators
Study Director: William V. Williams, M.D. Incyte Corporation
  More Information

No publications provided

Responsible Party: Incyte Corporation
ClinicalTrials.gov Identifier: NCT01858883     History of Changes
Other Study ID Numbers: INCB 39110-116
Study First Received: May 14, 2013
Last Updated: August 23, 2013
Health Authority: United States: Food and Drug Administration

Additional relevant MeSH terms:
Neoplasm Metastasis
Neoplasms
Neoplasms, Second Primary
Pancreatic Neoplasms
Neoplastic Processes
Pathologic Processes
Digestive System Neoplasms
Neoplasms by Site
Endocrine Gland Neoplasms
Digestive System Diseases
Pancreatic Diseases
Endocrine System Diseases
Gemcitabine
Paclitaxel
Antimetabolites, Antineoplastic
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Antineoplastic Agents
Therapeutic Uses
Antiviral Agents
Anti-Infective Agents
Enzyme Inhibitors
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Radiation-Sensitizing Agents
Tubulin Modulators
Antimitotic Agents
Mitosis Modulators

ClinicalTrials.gov processed this record on July 20, 2014