- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (22)
		
	   		
	   		    
                    
                   	
                   	    5 result(s) found for: ARAF.
                    
                
			
   			
		
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| EudraCT Number: 2014-002209-39 | Sponsor Protocol Number: M14LTK | Start Date*: 2014-07-30 | 
| Sponsor Name:The Netherlands Cancer Institute | ||
| Full Title: Phase I/II study with lapatinib plus trametinib in patients with metastatic KRAS mutant non-small cell lungcancer | ||
| Medical condition: non-small cell lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003299-10 | Sponsor Protocol Number: M13DAP | Start Date*: 2014-01-14 | 
| Sponsor Name:The Netherlands Cancer Institute | ||
| Full Title: Phase I/II study with the combination of dacomitinib and PD-0325901 in metastatic KRAS mutation positive non-small cell lung cancer | ||
| Medical condition: non-small cell lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004841-17 | Sponsor Protocol Number: NEO-TIM | Start Date*: 2020-08-18 | |||||||||||
| Sponsor Name:FONDAZIONE MELANOMA ONLUS | |||||||||||||
| Full Title: A phase II randomized non-comparative study, with neoadjuvant plus adjuvant therapy with combination or sequence of vemurafenib, cobImetinib, and atezolizuMab in patients with high-risk, surgically... | |||||||||||||
| Medical condition: high-risk, surgically resectable BRAF mutated and wild-type melanoma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004745-24 | Sponsor Protocol Number: MCLA-158-CL01 | Start Date*: 2018-02-22 | ||||||||||||||||
| Sponsor Name:Merus N.V. | ||||||||||||||||||
| Full Title: Phase 1/2 dose escalation and cohort expansion study evaluating MCLA-158 (Petosemtamab) as single agent or in combination in advanced solid tumors | ||||||||||||||||||
| Medical condition: Metastatic colorectal cancer Advanced solid tumors | ||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Trial now transitioned) NL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-005875-17 | Sponsor Protocol Number: CMEK162X2110 | Start Date*: 2012-05-30 | 
| Sponsor Name:Array Biopharma Inc | ||
| Full Title: A Phase Ib/II, multicenter, open-label, dose escalation study of LGX818 in combination with MEK162 in adult patients with BRAF V600 - dependent advanced solid tumors | ||
| Medical condition: Patients with solid tumors harboring a BRAF V600 mutation. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) IT (Completed) BE (Completed) FR (Ongoing) | ||
| Trial results: View results | ||
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