Autopsy report · NCT03114319
Dose Finding Study of TNO155 in Adult Patients With Advanced Solid Tumors
Cause of deathFunding or business
“Business reasons and not due to any safety concerns”
Life of this trial
- Registered 1 month before it started.
- Ran for about 8 years 1 month before it stopped.
- 227 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry
- Conditions
- Advanced EGFR Mutant Non Small Cell LungCancer (NSCLC); KRAS G12-mutant NSCLC; Esophageal Squamous Cell Cancer (SCC); Head/Neck SCC; Melanoma; Advanced Gastrointestinal Stromal Tumors (GIST)
- Interventions
- TNO155; TNO155 in combination with EGF816 (nazartinib)
- Participants
- 227
- Sites
- 18
- Countries
- Canada, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Taiwan, United States
Trials that died the same way
- Platform Study of JDQ443 in Combinations in Patients With Advanced Solid Tumors Harboring the KRAS G12C Mutation
“Business reasons and not based on any safety concerns.” - Phase 1/2 Study of USL311 +/- Lomustine in Advanced Solid Tumors or Relapsed/Recurrent Glioblastoma Multiforme (GBM)
“Business reasons not related to safety” - A Study to Assess AMG 701 Montherapy, or in Combination With Pomalidomide, With or Without, Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma
“business decision, not safety reasons.” - An Efficacy and Safety Study Evaluating the Fixed-Dose Combination of Candesartan Plus Amlodipine in Participants With Mild/Moderate Essential Hypertension
“Business reasons unrelated to product safety” - AGN-242428 in the Treatment of Plaque Psoriasis
“safety reason”
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.