- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4,039)
		
	   		
	   		    
                    
                   	
                   	    43 result(s) found for: ATM.
                    
                
			
   			
		
		Displaying page 1 of 3.
	
	
	| EudraCT Number: 2015-002726-39 | Sponsor Protocol Number: D4910C00009/C3601001 | Start Date*: 2016-02-25 | 
| Sponsor Name:Pfizer Inc. | ||
| Full Title: A Phase IIa prospective, open-label, multicenter study to determine the pharmacokinetics (PK) and safety and tolerability of aztreonam-avibactam (ATM-AVI) for the treatment of complicated Intra-Abd... | ||
| Medical condition: Complicated Intra-Abdominal Infections (cIAIs) in hospitalized adults | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000345-39 | Sponsor Protocol Number: B9991032 | Start Date*: 2019-02-19 | ||||||||||||||||
| Sponsor Name:Pfizer Inc. | ||||||||||||||||||
| Full Title: A Phase 2 Study to Evaluate Safety and Anti-tumor Activity of Avelumab in Combination with Talazoparib In Patients with BRCA or ATM Mutant Tumors | ||||||||||||||||||
| Medical condition: locally advanced (primary or recurrent) or metastatic solid tumors with a pathogenic or likely pathogenic germline or loss-of-function somatic BRCA1, or BRCA2, or ATM gene defect | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) BE (Completed) DK (Completed) ES (Ongoing) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-004544-38 | Sponsor Protocol Number: C3601009 | Start Date*: 2020-07-03 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: A PROSPECTIVE, RANDOMIZED, OPEN-LABEL, COMPARATIVE STUDY TO ASSESS THE EFFICACY, SAFETY AND TOLERABILITY OF AZTREONAM-AVIBACTAM (ATM-AVI) AND BEST AVAILABLE THERAPY FOR THE TREATMENT OF SERIOUS INF... | |||||||||||||
| Medical condition: SERIOUS INFECTIONS DUE TO MULTI-DRUG RESISTANT GRAM- NEGATIVE BACTERIA PRODUCING METALLO-Β-LACTAMASE (MBL) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Prematurely Ended) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003126-25 | Sponsor Protocol Number: MS201923-0001 | Start Date*: 2012-09-27 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: An Open-Label, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics of VX-970/M6620 in Combination With Cytotoxic Chemotherapy in Participants With Advanced Solid Tumors | |||||||||||||
| Medical condition: cancer (malignant solid tumors) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022315-19 | Sponsor Protocol Number: IEDAT-ERY01-2010 | Start Date*: 2011-01-11 | |||||||||||
| Sponsor Name:ERYDEL S.P.A. | |||||||||||||
| Full Title: Valutazione degli effetti del Desametasone Sodio Fosfato Intra-Eritrocitario sui Sintomi Neurologici in Pazienti con Atassia Teleangectasia | |||||||||||||
| Medical condition: Patients with Ataxia-Teleangectasia (AT) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001940-25 | Sponsor Protocol Number: IFG-05-2019 | Start Date*: 2021-08-25 | |||||||||||||||||||||||||||||||
| Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||||||||||||||||||||||
| Full Title: A PHASE II OPEN-LABEL STUDY FOR THE COMPREHENSIVE ANALYSIS OF PREDICTORS OF THE TREATMENT WITH PEMBROLIZUMAB AND OLAPARIB IN PATIENTS WITH UNRESECTABLE OR METASTATIC HER2 NEGATIVE BREAST CANCER AND... | |||||||||||||||||||||||||||||||||
| Medical condition: patients with unresectable or metastatic HER2 negative breast cancer and a deleterious germline mutation in BRCA 1/2, ATM, BARD1, CHEK2, FANCC, PALB2, RAD51C, RAD51D, SLX4, XRCC2 or a homologous re... | |||||||||||||||||||||||||||||||||
| 
 | |||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-004484-39 | Sponsor Protocol Number: BAY1895344/18594 | Start Date*: 2017-07-18 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: An open-label, first-in-human, dose-escalation study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and maximum tolerated dose and / or recommended Phase II dose of the A... | |||||||||||||
| Medical condition: Part A+A.1: Histologically confirmed solid tumors or NHL Part A J-arm : Advanced solid tumors Part B: a) DDR deficient advanced solid tumors: i) CRPC; ii) HER2- negative BC (estrogen-receptor posit... | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002529-27 | Sponsor Protocol Number: D5339C00001 | Start Date*: 2021-02-24 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Modular Phase 2a Multicentre Open-Label Study to Investigate DNA-damage Response Agents (or Combinations) in Patients With Advanced Cancer Whose Tumours Contain Molecular Alterations (PLANETTE) | |||||||||||||
| Medical condition: Advanced Cancer Whose Tumours Contain Molecular Alterations | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-003472-14 | Sponsor Protocol Number: ART0380C001 | Start Date*: 2022-07-04 | |||||||||||
| Sponsor Name:Artios Pharma Limited | |||||||||||||
| Full Title: A Phase I/IIa, Open-label, Multi-center Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the ATR Kinase Inhibitor ART0380 Administered Orally as Monotherapy an... | |||||||||||||
| Medical condition: Advanced or Metastatic Solid Tumours | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003899-13 | Sponsor Protocol Number: NL65803.078.18 | Start Date*: 2018-12-20 | 
| Sponsor Name: | ||
| Full Title: The effect of IntraDialytic Parenteral Nutrition on nutritional status and quality of life in hemodialysis patients | ||
| Medical condition: Malnutrition / Sarcopenia (loss of muscle mass) in hemodialyse patients. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003785-24 | Sponsor Protocol Number: C15-050TRAVEL | Start Date*: 2014-10-02 | |||||||||||
| Sponsor Name:Uzsoki Utcai Kórház | |||||||||||||
| Full Title: Treatment of pancreatic adenocarcinoma with the combinationof carboplatin and velparib | |||||||||||||
| Medical condition: pancreatic adenocarcinoma | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000300-28 | Sponsor Protocol Number: D081DC00007 | Start Date*: 2017-02-24 | ||||||||||||||||
| Sponsor Name:AstraZeneca | ||||||||||||||||||
| Full Title: A Phase III, Open Label, Randomized Study to Assess the Efficacy and Safety of Olaparib (Lynparza™) Versus Enzalutamide or Abiraterone Acetate in Men with Metastatic Castration-Resistant Prostate C... | ||||||||||||||||||
| Medical condition: Metastatic castration-resistant prostate cancer | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: SE (Completed) DK (Completed) NO (Completed) ES (Completed) AT (Completed) FR (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-003162-13 | Sponsor Protocol Number: CO-338-052 | Start Date*: 2017-02-10 | ||||||||||||||||
| Sponsor Name:Clovis Oncology, Inc. | ||||||||||||||||||
| Full Title: TRITON2: A Multicenter, Open-label Phase 2 Study of Rucaparib in Patients with Metastatic Castration-resistant Prostate Cancer Associated with Homologous Recombination Deficiency | ||||||||||||||||||
| Medical condition: Metastatic castration-resistant prostate cancer | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) IE (Completed) ES (Completed) BE (Completed) DK (Completed) FR (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-001205-73 | Sponsor Protocol Number: IMP4297-202 | Start Date*: 2021-08-24 | ||||||||||||||||
| Sponsor Name:IMPACT Therapeutics, Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double-Blinded, Placebo-Controlled, Multicenter, Phase II Study to Evaluate Senaparib Maintenance in mCRPC Patients with Homologous Recombination Repair Gene Alterations after Docetax... | ||||||||||||||||||
| Medical condition: metastatic castration-resistant prostate cancer (mCRPC) | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: BE (Completed) FR (Completed) ES (Ongoing) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-004830-32 | Sponsor Protocol Number: ICPCT-2011-UA-FF | Start Date*: 2012-01-27 | |||||||||||
| Sponsor Name:FAES FARMA, S.A. | |||||||||||||
| Full Title: Effects of bilastine on nasal volume after allergen-induced rhinitis in patients with allergic rhinitis | |||||||||||||
| Medical condition: Allergic Rhinitis | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002617-39 | Sponsor Protocol Number: Fondazione Mediolanum 001/2007 | Start Date*: 2008-01-23 | |||||||||||
| Sponsor Name:Fondazione Mediolanum Onlus | |||||||||||||
| Full Title: INtegrilin plus STenting to Avoid Myocardial Necrosis Trial | |||||||||||||
| Medical condition: Patients with diffuse CAD undergoing percutaneous treatment on a native coronary vessel with planned implantation of two DES in overlapping with a total stent length 33 mm for diffuse coronary dis... | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002966-37 | Sponsor Protocol Number: 1-2018BSMO | Start Date*: 2019-01-23 | 
| Sponsor Name:Belgian Society of Medical Oncology | ||
| Full Title: Efficacy of Olaparib in advanced cancers occurring in patients with germline mutations or somatic tumor mutations in homologous recombination genes. | ||
| Medical condition: Advanced cancer patients that have a germline mutation or a somatic mutation in their tumor. Prostate and ovarian cancer patients and breast cancer patients who carry a BRCA1/2 mutation will be exc... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000338-36 | Sponsor Protocol Number: IEDAT-03-2018 | Start Date*: 2018-05-31 | |||||||||||
| Sponsor Name:EryDel S.p.A. | |||||||||||||
| Full Title: Open-label, Long-term, Extension Treatment using Intra-Erythrocyte Dexamethasone Sodium Phosphate in Patients with Ataxia Telangiectasia Who Participated in the IEDAT-02-2015 Study | |||||||||||||
| Medical condition: Patient with neurological symptoms of Ataxia Telangiectasia | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) BE (Completed) PL (Completed) GB (GB - no longer in EU/EEA) NO (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005241-31 | Sponsor Protocol Number: IEDAT-02-2015 | Start Date*: 2016-09-14 | |||||||||||
| Sponsor Name:EryDel S.p.A. | |||||||||||||
| Full Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Effects of Intra-Erythrocyte Dexamethasone Sodium Phosphate on Neurological Symptoms in Patients with Ataxia Telan... | |||||||||||||
| Medical condition: Patient with neurological symptoms of Ataxia Telangiectasia | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) NO (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003520-37 | Sponsor Protocol Number: D081DC00008 | Start Date*: 2014-02-04 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Randomised, Double-Blind, Placebo-Controlled, Multicentre Phase II Study to Compare the Efficacy, Safety and Tolerability of Olaparib Versus Placebo When Given in Addition to Abiraterone Treatmen... | |||||||||||||
| Medical condition: metastatic castrate-resistant prostate cancer | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) NL (Completed) CZ (Completed) ES (Completed) IT (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
			Subscribe to this Search
To subscribe to the RSS feed for this search click here .
			This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
			.
			This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
		
			
To subscribe to the RSS feed for this search click here
 .
			This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
			.
			This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
		| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
 Query did not match any studies.
    	Query did not match any studies.
     
				
