Autopsy report · NCT02468661
A Safety and Efficacy Study of INC280 Alone, and in Combination With Erlotinib, Compared to Chemotherapy, in Advanced/Metastatic Non-small Cell Lung Cancer Patients With EGFR Mutation and cMET Amplification
Cause of deathSlow enrollment
“Major challenge for enrollment of participants.”
Life of this trial
- Registered 4 months before it started.
- Ran for about 3 years 2 months before it stopped.
- 23 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry
- Conditions
- Non-Small Cell Lung Cancer
- Interventions
- INC280 single agent; erlotinib
- Participants
- 23
- Sites
- 32
- Countries
- Belgium, France, Germany, Italy, Japan, Netherlands, Singapore, South Korea, Spain, United States
Trials that died the same way
- Angiotensin II for Distributive Shock
“Enrollment Challenges” - Study of Neoadjuvant Imprime PGG and Pembrolizumab for Stage III, Resectable Melanoma
“Enrollment challenges, study not feasible” - Neoadjuvant HAIC of TACE Plus Donafenib in BCLC B Stage HCC: a Multi-center Randomized Controlled Trial.
“Difficult to enroll participants” - Extended Treatment With Vancomycin for Clostridium Difficile Colitis
“Difficult enrollment” - The Safety of Transdermal Nicotine Immediately Following an Acute Coronary Syndrome
“Difficulties with enrollment.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.