ICH GCP - EU Clinical trials Registry

EudraCT Number: 2006-005520-16

Sponsor Protocol Number: BO20603

Start Date: 2007-05-02

Sponsor Name: F. Hoffmann-La Roche Ltd

Full Title: Ensayo clínico de fase III multicéntrico, randomizado, doble ciego, controlado con placebo, para comparar la eficacia de bevacizumab en combinación con rituximab y CHOP (RA CHOP) frente a rituxima...

Medical condition: Pacientes con linfoma difuso de células B grandes (LDCBG) CD20-positivo no tratados previamente, que presentan enfermedad de riesgo intermedio-bajo, intermedio-alto o alto, de acuerdo con el índic...

Disease:	Version	SOC Term	Classification Code	Term	Level
	8.1		10012818	Diffuse large B-cell lymphoma	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: ES (Temporarily Halted) AT (Completed) FR (Ongoing) CZ (Ongoing) GR (Ongoing) PT (Completed) GB (Completed) SE (Completed) DE (Completed) IT (Completed) PL (Completed) SK (Ongoing) LT (Completed) HU (Ongoing)

Trial results: View results

EudraCT Number: 2005-000077-22

Sponsor Protocol Number: CL2-90652-001

Start Date:

Sponsor Name: Institut de Recherches Internationales Servier

Full Title: Acceptability, safety, pharmacokinetics and effects on blood pressure of a daily dose of 0.025 to 0.135 milligram per kilogram of S 90652, a paediatric formulation of perindopril, in 2-16 years old...

Medical condition: Arterial hypertension

Disease:	Version	SOC Term	Classification Code	Term	Level
	5.1		10020782		PT

Population Age: Children, Adolescents, Under 18

Gender: Male, Female

Trial protocol: BE (Completed) IT (Completed)

Trial results: View results

EudraCT Number: 2004-003035-31

Sponsor Protocol Number: KF4248/05

Start Date: 2005-07-06

Sponsor Name: Grünenthal GmbH [...] 1. Grünenthal GmbH 2. Laboratorios Andrómaco S.A. (Co-sponsor Spanien)

Full Title: Safety of the oral monophasic contraceptive GRT4248 (0.02 mg ethinylestradiol/2 mg chlormadinone acetate) in comparison to 0.02 mg ethinylestradiol/0.15 mg desogestrel given for 6 medication cycles...

Medical condition: Contraception

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults

Gender: Female

Trial protocol: DE (Completed) IT (Completed) ES (Completed)

Trial results: View results

EudraCT Number: 2004-003055-40

Sponsor Protocol Number: SON-8184-1073

Start Date: 2005-08-23

Sponsor Name: SONUS Pharmaceuticals Inc.

Full Title: A PHASE 2 MULTICENTER EVALUATION OF THE SAFETY AND EFFICACY OF TOCOSOL ® PACLITAXEL (S-8184 PACLITAXEL INJECTABLE EMULSION) IN PATIENTS WITH METASTATIC OR LOCALLY ADVANCED, UNRESECTABLE TRANSITIONA...

Medical condition: PATIENTS WITH METASTATIC OR LOCALLY ADVANCED, UNRESECTABLE TRANSITIONAL CELL CARCINOMA OF THE UROTHELIUM

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: GB (Ongoing) ES (Ongoing)

Trial results: (No results available)

EudraCT Number: 2004-000866-11

Sponsor Protocol Number: 7164-L-01

Start Date: 2004-08-06

Sponsor Name: ZAMBON GROUP

Full Title: A multicenter, randomized, parallel group, controlled, double-blind study to evaluate efficacy and safety of pholcodine as antitussive agent vs dextrometorphan in non-productive cough

Medical condition: Symptomatic treatment of non productive cough

Disease:	Version	SOC Term	Classification Code	Term	Level
	6.1		10011224		PT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: IT (Completed)

Trial results: View results

EudraCT Number: 2004-002850-69

Sponsor Protocol Number: IGPM01

Start Date: 2006-01-06

Sponsor Name: Swansea NHS Trust

Full Title: Role of High dose insulin and glucose-potassium-magnesium (HDI-GKM) for Myocardial protection in cardiac surgery

Medical condition: We propose to recruit 90 patients (based on the power calculation) undergoing first time urgent in-house CABG at Morriston Hospital. The decision to operate on an urgent basis will be based on the ...

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: GB (Prematurely Ended)

Trial results: (No results available)

EudraCT Number: 2004-002852-33

Sponsor Protocol Number: TOR-RIS-2004-01

Start Date: 2005-04-13

Sponsor Name: Dr. Jose Vicente Torregrosa Prats (fundacio clinic)

Full Title: a randomised, open clinical trial to study the efficacy of risedronate 35 mg/week in prevention of bone mass loss and vascular calcifications after kidney transplantation Ensayo aleatorio, abierto ...

Medical condition: bone metabolic pathology associated to kidney transplantation

Disease:	Version	SOC Term	Classification Code	Term	Level
	7.1		10058972		LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: ES (Ongoing)

Trial results: (No results available)

EudraCT Number: 2004-002871-18

Sponsor Protocol Number: A-92-52030-166

Start Date: 2006-02-09

Sponsor Name: IPSEN PHARMA, S.A.

Full Title: Phase II, open, single group,multicentre study to evaluate the efficacy and safety of Somatuline Autogel® (120 mg) administered every 4 weeks by deep subcutaneous injection in the tumour´s growth s...

Medical condition: Patients with progressive neuroendocrine tumours who are not eligible to be treated with either surgery or chemotherapy

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: ES (Completed)

Trial results: View results

EudraCT Number: 2004-002887-41

Sponsor Protocol Number: OV-W05

Start Date: 2004-12-01

Sponsor Name: OmniVision GmbH

Full Title: Randomisierte, kontrollierte, für den Prüfer verblindete klinische Prüfung (Pilotstudie) zur Untersuchung der Wirksamkeit von Spersadex® Augentropfen im Vergleich zu Isopto®-Dex Augentropfen bei Pa...

Medical condition: Nicht-infektiöse Conjunctivitis

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults

Gender: Male, Female

Trial protocol: DE (Completed)

Trial results: View results

EudraCT Number: 2004-004136-31

Sponsor Protocol Number: EF489-2004/1

Start Date: 2005-07-08

Sponsor Name: Laboratorios Effik, S.A.

Full Title: Ensayo clínico para evaluar la eficacia de los suplementos de progesterona natural en la prevención del parto pretérmino gemelar

Medical condition: Parto pretérmino en embarazos gemelares

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults

Gender: Female

Trial protocol: ES (Completed)

Trial results: (No results available)