LDK378 Versus Chemotherapy in ALK Rearranged (ALK Positive) Patients Previously Treated With Chemotherapy (Platinum Doublet) and Crizotinib
| Status: | Active, not recruiting | 
|---|---|
| Conditions: | Lung Cancer, Cancer | 
| Therapuetic Areas: | Oncology | 
| Healthy: | No | 
| Age Range: | 18 - Any | 
| Updated: | 1/10/2019 | 
| Start Date: | June 28, 2013 | 
| End Date: | May 26, 2021 | 
A Phase III, Multicenter, Randomized, Open-label Study of Oral LDK378 Versus Standard Chemotherapy in Adult Patients With ALK-rearranged (ALK-positive) Advanced Non-small Cell Lung Cancer Who Have Been Treated Previously With Chemotherapy (Platinum Doublet) and Crizotinib
The primary purpose of the study was to compare the antitumor activity of LDK378 vs.
chemotherapy in patients previously treated with chemotherapy (platinum doublet) and
crizotinib.
			chemotherapy in patients previously treated with chemotherapy (platinum doublet) and
crizotinib.
Inclusion Criteria:
1. Patient has a histologically or cytologically confirmed diagnosis of non-small cell
lung cancer (NSCLC) that is anaplastic lymphoma kinase (ALK) positive as assessed by
the FDA approved Abbott FISH Test.
2. Patient has stage IIIB or IV diagnosis and must have received one or two prior
regimens (including platinum- doublet) of cytotoxic chemotherapy for the treatment of
locally advanced or metastatic NSCLC.
3. Patient has at least one measurable lesion as defined by RECIST 1.1. A previously
irradiated site lesion may only be counted as a target lesion if there is clear sign
of progression since the irradiation
4. Patients must have received previous treatment with crizotinib for the treatment of
locally advanced or metastatic NSCLC.
Exclusion Criteria:
1. Patient with known hypersensitivity to any of the excipients of LDK378
(microcrystalline cellulose, mannitol, crospovidone, colloidal silicon dioxide and
magnesium stearate)
2. Patient with a history of severe hypersensitivity reaction to pemetrexed or docetaxel
or any known excipients of these drugs.
3. Patient with symptomatic central nervous system (CNS) metastases who is neurologically
unstable or has required increasing doses of steroids within the 2 weeks prior to
screening to manage CNS symptoms.
We found this trial at
    18
    sites
	
								Miami, Florida 33136			
	
			
					Principal Investigator: Israel Wiznitzer
			
						
										Phone: 305-243-4624
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								Boston, Massachusetts 02114			
	
			
					Principal Investigator: Alice Shaw
			
						
										Phone: 617-724-1223
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								Fairfax, Virginia 22031			
	
			
					Principal Investigator: Alexander Spira
			
						
										Phone: 703-208-3174
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								Jacksonville, Florida 32256			
	
			
					Principal Investigator: Safeer Ashraf
			
						
										Phone: 904-538-3667
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								Maywood, Illinois 60153			
	
			
					Principal Investigator: Kathy Albain
			
						
										Phone: 708-327-3222
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								Nashville, Tennessee 37203			
	
			
					Principal Investigator: David R. Spigel
			
						
										Phone: 615-329-7274
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								Seattle, Washington 98104			
	
			
					Principal Investigator: Howard L. (Jack) West
			
						
										Phone: +1 206 386 2443
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								Waco, Texas 76712			
	
			
					Principal Investigator: Carl Chakmakjian
			
						
										Phone: 254-399-0741
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								Wenatchee, Washington 98801			
	
			
					Principal Investigator: Mitchell Garrison
			
						
										Phone: 509-665-5800
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