DS-8201a in Human Epidermal Growth Factor Receptor 2 (HER2)-Expressing or -Mutated Non-Small Cell Lung Cancer
| Status: | Recruiting | 
|---|---|
| Conditions: | Lung Cancer, Lung Cancer, Cancer | 
| Therapuetic Areas: | Oncology | 
| Healthy: | No | 
| Age Range: | 18 - Any | 
| Updated: | 3/31/2019 | 
| Start Date: | May 21, 2018 | 
| End Date: | October 30, 2020 | 
| Contact: | (for Asia Sites Only) Daiichi Sankyo Contact for Clinical Trial Information | 
| Email: | dsclinicaltrial@daiichisankyo.co.jp | 
| Phone: | +81-3-6225-1111(M-F 9-5 JST) | 
A Phase 2, Multicenter, Open-Label, 2-Cohort Study of Trastuzumab Deruxtecan (DS-8201a), an Anti-HER2 Antibody Drug Conjugate (ADC), for HER2-Over-Expressing or -Mutated, Unresectable and/or Metastatic Non Small Cell Lung Cancer (NSCLC)
The primary objective of this trial is to evaluate the efficacy of trastuzumab deruxtecan in
HER2-over-expressing and/or HER2-mutated advanced NSCLC subjects.
			HER2-over-expressing and/or HER2-mutated advanced NSCLC subjects.
Inclusion Criteria:
- Age ≥20 years old in Japan, ≥18 years old in other countries
- Pathologically documented unresectable and/or metastatic non-squamous NSCLC
- Has relapsed from or is refractory to standard treatment or for which no standard
treatment is available
- For Cohort 1 only: HER2-overexpression (IHC 2+ or 3+) status must be assessed and
confirmed by Clinical Laboratory Improvement Amendments (CLIA)-certified laboratory or
equivalent, from an archival tumor sample
- For Cohort 2 only: Documented any known activating HER2 mutation from an archival
tumor sample analyzed by CLIA laboratory or equivalent
- Presence of at least 1 measurable lesion assessed by the investigator based on
Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
- Is willing and able to provide an adequate archival tumor sample
- Is willing to undergo a tissue biopsy, after the completion of the most recent
treatment regimen
- Has Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 to 1
Exclusion Criteria:
- Was previously treated with HER2-targeted therapies, except for pan-HER class tyrosine
kinase inhibitors
- For Cohort 1 only: Has known HER2 mutation
- Has a medical history of myocardial infarction, symptomatic congestive heart failure
(CHF) (NYHA classes II-IV), unstable angina or serious cardiac arrhythmia
- Has a QTc prolongation to > 450 millisecond (ms) in males and > 470 ms in females
- Has a medical history of clinically significant lung disease
- Is suspected to have certain other protocol-defined diseases based on imaging at
screening period
- Has history of any disease, metastatic condition, drug/medication use or other
condition that might, per protocol or in the opinion of the investigator, compromise:
1. safety or well-being of the participant or offspring
2. safety of study staff
3. analysis of results
We found this trial at
    8
    sites
	
		Univ of Washington Founded in 1861 by a private gift of 10 acres in what...  
  
  Click here to add this to my saved trials
	
		University of Michigan The University of Michigan was founded in 1817 as one of the...  
  
  Click here to add this to my saved trials
	
									450 Brookline Ave
Boston, Massachusetts 2215
	
			Boston, Massachusetts 2215
617-632-3000 
							
					Phone: 617-632-6036
					
		Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...  
  
  Click here to add this to my saved trials
	Click here to add this to my saved trials
	Click here to add this to my saved trials
	
									1275 York Ave
New York, New York 10021
	
			New York, New York 10021
(212) 639-2000
							
					Phone: 646-888-4201
					
		Memorial Sloan Kettering Cancer Center Memorial Sloan Kettering Cancer Center — the world's oldest and...  
  
  Click here to add this to my saved trials
	Click here to add this to my saved trials
	Click here to add this to my saved trials