search
Back to results

Study of Salirasib to Treat Non-Small Cell Lung Cancer

Primary Purpose

Carcinoma, Non-Small-Cell Lung

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Salirasib
Sponsored by
Concordia Pharmaceuticals, Inc
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Carcinoma, Non-Small-Cell Lung focused on measuring Non-Small-Cell Lung

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 or older
  • Non-Small Cell Lung Cancer not amenable to curative therapy with surgery or radiation
  • Measurable disease
  • Adenocarinoma of the lung, have not received prior chemotherapy for the malignancy and has a ≥ 15 pack year history of smoking; OR previously treated with recurrent disease and documented KRAS mutation
  • Last dose of radiotherapy > 3 weeks prior to study entry and recovered from all acute toxicities associated with the prior therapy
  • No history of another malignancy in the past 5 years except treated non-melanomatous skin cancer or superficial bladder cancer or carcinoma-in-situ of the cervix
  • Karnofsky Performance status of 70 or greater
  • Body Weight > 50 kg
  • Life expectancy ≥ 3 months
  • Serum Creatinine ≤2.0 mg/dL, total bilirubin ≤ 2.0 mg/dL, ALT and AST ≤ 3x ULN, alkaline phosphatase ≤ 5x ULN, WBC > 3000/mm³, ANC ≥ 1500/mm³, platelets ≥ 100,000/mm³, hemoglobin ≥ 10g/dL.
  • No coexisting cardiac or medical problems that would limit compliance in the study
  • Willing to undergo blood sampling for pharmacokinetic analysis
  • Negative pregnancy test, if applicable

Exclusion Criteria:

  • Evidence of active heart disease including myocardial infarction within previous 3 months
  • Active infectious process
  • Active central nervous system metastases (requiring increasing doses of corticosteroids over the prior month, known progressing lesions)
  • Pregnant or lactating
  • Major surgery without full recovery or major surgery within 3 weeks prior to treatment start
  • QTc Interval > 470 msec
  • Gastrointestinal tract disease resulting in inability to take or absorb oral medications

Sites / Locations

  • Memorial Sloan Kettering Cancer Center

Outcomes

Primary Outcome Measures

Rate of non-progression (as reflected in the tumor control rate of percent patients with CR+PR+SD) defined as the number of patients whose tumor did not progress (<20% tumor increase to total disappearance of tumor according to RECIST)

Secondary Outcome Measures

Full Information

First Posted
September 17, 2007
Last Updated
June 8, 2011
Sponsor
Concordia Pharmaceuticals, Inc
search

1. Study Identification

Unique Protocol Identification Number
NCT00531401
Brief Title
Study of Salirasib to Treat Non-Small Cell Lung Cancer
Official Title
Salirasib for Treatment of Advanced Non-Small Cell Lung Cancer: a Phase II Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Concordia Pharmaceuticals, Inc

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether Salirasib is effective to shrink or prevent the growth of the tumors associated with non-small cell lung cancer in both patients who are newly diagnosed or have recurrent disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Non-Small-Cell Lung
Keywords
Non-Small-Cell Lung

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
71 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Salirasib
Intervention Description
600mg BID until disease progression or unacceptable toxicity occurs.
Primary Outcome Measure Information:
Title
Rate of non-progression (as reflected in the tumor control rate of percent patients with CR+PR+SD) defined as the number of patients whose tumor did not progress (<20% tumor increase to total disappearance of tumor according to RECIST)
Time Frame
10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 or older Non-Small Cell Lung Cancer not amenable to curative therapy with surgery or radiation Measurable disease Adenocarinoma of the lung, have not received prior chemotherapy for the malignancy and has a ≥ 15 pack year history of smoking; OR previously treated with recurrent disease and documented KRAS mutation Last dose of radiotherapy > 3 weeks prior to study entry and recovered from all acute toxicities associated with the prior therapy No history of another malignancy in the past 5 years except treated non-melanomatous skin cancer or superficial bladder cancer or carcinoma-in-situ of the cervix Karnofsky Performance status of 70 or greater Body Weight > 50 kg Life expectancy ≥ 3 months Serum Creatinine ≤2.0 mg/dL, total bilirubin ≤ 2.0 mg/dL, ALT and AST ≤ 3x ULN, alkaline phosphatase ≤ 5x ULN, WBC > 3000/mm³, ANC ≥ 1500/mm³, platelets ≥ 100,000/mm³, hemoglobin ≥ 10g/dL. No coexisting cardiac or medical problems that would limit compliance in the study Willing to undergo blood sampling for pharmacokinetic analysis Negative pregnancy test, if applicable Exclusion Criteria: Evidence of active heart disease including myocardial infarction within previous 3 months Active infectious process Active central nervous system metastases (requiring increasing doses of corticosteroids over the prior month, known progressing lesions) Pregnant or lactating Major surgery without full recovery or major surgery within 3 weeks prior to treatment start QTc Interval > 470 msec Gastrointestinal tract disease resulting in inability to take or absorb oral medications
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gregory J Riely, MD PhD
Organizational Affiliation
Memorial Sloan Kettering Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Memorial Sloan Kettering Cancer Center
City
New York
State/Province
New York
ZIP/Postal Code
10017
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Study of Salirasib to Treat Non-Small Cell Lung Cancer

We'll reach out to this number within 24 hrs