EU Clinical Trials Register [PDF]

Feb 26, 2015 - Ensayo clínico para evaluar al seguridad de un gel vaginal que contiene estriol 0.005%, en mujeres menop

22 downloads 22 Views 70KB Size

Recommend Stories


Clinical Trials
Live as if you were to die tomorrow. Learn as if you were to live forever. Mahatma Gandhi

Clinical Trials
Don't count the days, make the days count. Muhammad Ali

clinical trials
This being human is a guest house. Every morning is a new arrival. A joy, a depression, a meanness,

Clinical Trials
You often feel tired, not because you've done too much, but because you've done too little of what sparks

Clinical Trials
When you talk, you are only repeating what you already know. But if you listen, you may learn something

Clinical Trials
This being human is a guest house. Every morning is a new arrival. A joy, a depression, a meanness,

Clinical trials
You're not going to master the rest of your life in one day. Just relax. Master the day. Than just keep

Clinical Trials
Be like the sun for grace and mercy. Be like the night to cover others' faults. Be like running water

PDF Clinical Trials in Cardiovascular Disease
Why complain about yesterday, when you can make a better tomorrow by making the most of today? Anon

Clinical Trials in Estonia
What you seek is seeking you. Rumi

Idea Transcript


EU Clinical Trials Register Home & Search

Joining a trial

Contacts

Help

About

Clinical trials The European Union Clinical Trials Register allows you to search for protocol and results information on: interventional clinical trials that are conducted in the European Union (EU) and the European Economic Area (EEA); clinical trials conducted outside the EU / EEA that are linked to European paediatric-medicine development. Learn more about the EU Clinical Trials Register including the source of the information and the legal basis. The EU Clinical Trials Register currently displays 32159 clinical trials with a EudraCT protocol, of which 5175 are clinical trials conducted with subjects less than 18 years old. The register also displays information on 18700 older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).



X

Please enter search term...

Search

Examples: Cancer AND drug name. Pneumonia AND sponsor name. How to search [pdf]

Advanced Search: Search tools

< Back to search results Summary EudraCT Number:

2014-004517-84

Sponsor's Protocol Code Number:

ITFE-2026-C10

National Competent Authority:

Spain - AEMPS

Clinical Trial Type:

EEA CTA

Trial Status:

Completed

Date on which this record was first entered in the EudraCT database:

2015-01-02

Trial results Index A. PROTOCOL INFORMATION B. SPONSOR INFORMATION C. APPLICANT IDENTIFICATION D. IMP IDENTIFICATION D.8 INFORMATION ON PLACEBO E. GENERAL INFORMATION ON THE TRIAL F. POPULATION OF TRIAL SUBJECTS G. INVESTIGATOR NETWORKS TO BE INVOLVED IN THE TRIAL N. REVIEW BY THE COMPETENT AUTHORITY OR ETHICS COMMITTEE IN THE COUNTRY CONCERNED P. END OF TRIAL A. Protocol Information A.1

Member State Concerned

Spain - AEMPS

A.2

EudraCT number

2014-004517-84

A.3

Full title of the trial

A PHASE II PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED AND MULTI-CENTRE CLINICAL TRIAL TO ASSESS THE SAFETY OF 0.005 % ESTRIOL VAGINAL GEL IN HORMONE RECEPTOR-POSITIVE POSTMENOPAUSAL WOMEN WITH EARLY STAGE BREAST CANCER IN TREATMENT WITH AROMATASE INHIBITOR IN THE ADJUVANT SETTING.? BLISSAFE Study? Ensayo clínico fase II, prospectivo, multicéntrico, aleatorizado, doble ciego y controlado con placebo para evaluar la seguridad del gel vaginal de estriol al 0.005% en mujeres postmenopáusicas con cáncer de mama en estadio precoz y receptores hormonales positivos en tratamiento adyuvante con inhibidores de aromatasa.

A.3.1

Title of the trial for lay people, in easily understood, i.e. nonClinical trial to evaluate the safety of a vaginal gel containing 0.005% of estriol, in hormone receptor-positive women in menopause technical, language with early stage breast cancer in treatment with aromatase inhibitor Ensayo clínico para evaluar al seguridad de un gel vaginal que contiene estriol 0.005%, en mujeres menopáusicas, con cáncer de mama en estadio precoz en tratamiento con inhibidores de aromatasa y receptores hormonales positivos

A.3.2

Name or abbreviated title of the trial where available

A.4.1

Sponsor's protocol code number

ITFE-2026-C10

A.7

Trial is part of a Paediatric Investigation Plan

No

A.8

EMA Decision number of Paediatric Investigation Plan

BLISSAFE

B. Sponsor Information B.Sponsor: 1 B.1.1

Name of Sponsor

ITF Research Pharma S.L.U

B.1.3.4

Country

Spain

B.3.1 and B.3.2

Status of the sponsor

Commercial

B.4 Source(s) of Monetary or Material Support for the clinical trial: B.4.1

Name of organisation providing support

ITF Research Pharma S.L.U.

B.4.2

Country

Spain

B.5 Contact point designated by the sponsor for further information on the trial B.5.1

Name of organisation

GEICAM Spanish Breast Cancer Group

B.5.2

Functional name of contact point

GEICAM

B.5.3

Address:

B.5.3.1

Street Address

Av de los Pirineos 7, 1ª Planta ? Oficina 1-3

B.5.3.2

Town/ city

San Sebastián de los Reyes (Madrid)

B.5.3.3

Post code

28703

B.5.3.4

Country

Spain

B.5.4

Telephone number

+34916592870

B.5.5

Fax number

+34916510406

B.5.6

E-mail

[email protected]

D. IMP Identification D.IMP: 1 D.1.2 and IMP Role D.1.3

Test

D.2

Status of the IMP to be used in the clinical trial

D.2.1

IMP to be used in the trial has a marketing authorisation

Yes

D.2.1.1.1

Trade name

Blissel

D.2.1.1.2

Name of the Marketing Authorisation holder

Italfarmaco S.A.

D.2.1.2

Country which granted the Marketing Authorisation

Spain

D.2.5

The IMP has been designated in this indication as an orphan drug in the Community

No

D.2.5.1

Orphan drug designation number

D.3 Description of the IMP D.3.4

Pharmaceutical form

Vaginal gel

D.3.4.1

Specific paediatric formulation

No

D.3.7

Routes of administration for this IMP

Vaginal use

D.3.8 to D.3.10 IMP Identification Details (Active Substances) D.3.8

INN - Proposed INN

ESTRIOL

D.3.9.2

Current sponsor code

ESTRIOL

D.3.9.4

EV Substance Code

SUB01971MIG

D.3.10

Strength

D.3.10.1

Concentration unit

% percent

D.3.10.2

Concentration type

equal

D.3.10.3

Concentration number

0.005

D.3.11 The IMP contains an: D.3.11.1

Active substance of chemical origin

Yes

D.3.11.2

Active substance of biological/ biotechnological origin (other No than Advanced Therapy IMP (ATIMP) The IMP is a:

D.3.11.3

Advanced Therapy IMP (ATIMP)

No

D.3.11.3.1 Somatic cell therapy medicinal product

No

D.3.11.3.2 Gene therapy medical product

No

D.3.11.3.3 Tissue Engineered Product

No

D.3.11.3.4 Combination ATIMP (i.e. one involving a medical device)

No

D.3.11.3.5 Committee on Advanced therapies (CAT) has issued a classification for this product

No

D.3.11.4

Combination product that includes a device, but does not involve an Advanced Therapy

Yes

D.3.11.5

Radiopharmaceutical medicinal product

No

D.3.11.6

Immunological medicinal product (such as vaccine, allergen, No immune serum)

D.3.11.7

Plasma derived medicinal product

No

D.3.11.8

Extractive medicinal product

No

D.3.11.9

Recombinant medicinal product

No

D.3.11.10 Medicinal product containing genetically modified organisms No D.3.11.11 Herbal medicinal product

No

D.3.11.12 Homeopathic medicinal product

No

D.3.11.13 Another type of medicinal product

No

D.8 Information on Placebo D.8 Placebo: 1 D.8.1

Is a Placebo used in this Trial?

Yes

D.8.3

Pharmaceutical form of the placebo

Vaginal gel

D.8.4

Route of administration of the placebo

Vaginal use

E. General Information on the Trial E.1 Medical condition or disease under investigation E.1.1

Medical condition(s) being investigated

In postmenopausal hormone receptor positive breast cancer, treatment with aromatase inhibitors is the most effective and wellstudied therapy. Lack of adherence is common due to the side-effects; vaginal dryness and vaginal atrophy. The study will explore the safety of 0.005% estriol vaginal gel in the oncological context, to demostrate that the gel is a safe option to treat the vaginal atrophy caused by AIs, without a significant decline in gonadotropin or increase in systemic estrogen levels En mujeres postmenopáusicas con cáncer de mama y receptores hormonales positivos , el tratamiento con inhibidores de la aromatasa es la terapia más eficaz pero produce efectos secundarios; sequedad y atrofia vaginal. El estudio explorará la seguridad del gel vaginal de estriol 0,005% en el contexto oncológico, para demostrar que es un tratamiento seguro para la atrofia vaginal causada por IAS, sin disminución significativa de gonadotropinas o aumento en los niveles sistémicos de estrógenos

E.1.1.1

Medical condition in easily understood language

Postmenopausal woman with breast cancer are treated with aromatase inhibitors. The problem is that causes many vaginal adverse events that may be treated safely with 0.005% estriol vaginal gel Mujeres postmenopáusicas con cáncer de mama se tratan con inhibidores de aromatasa, pero tienen efectos secundarios vaginales que podrías tratarse de manera segura con el gel vaginal de estriol 0,005%

E.1.1.2

Therapeutic area

Diseases [C] - Cancer [C04]

MedDRA Classification E.1.3

Condition being studied is a rare disease

No

E.2 Objective of the trial E.2.1

Main objective of the trial

To evaluate the levels of FSH after treatment with 0.005% estriol vaginal gel in hormone receptor-positive postmenopausal women with early stage breast cancer in treatment with NSAIs in the adjuvant setting and symptoms of vaginal atrophy Evaluar los niveles de FSH tras el tratamiento de los síntomas de la atrofia vaginal con el gel vaginal de estriol 0,005% en mujeres postmenopáusicas con cáncer de mama en estadio precoz y receptores hormonales positivos en tratamiento adyuvante con inhibidores de aromatasa.

E.2.2

Secondary objectives of the trial

To evaluate the levels of estriol, estradiol, estrone, FSH and LH after treatment with 0.005% estriol vaginal gel in hormone receptorpositive postmenopausal women with early stage breast cancer in treatment with NSAIs in the adjuvant setting and symptoms of vaginal atrophy. To assess the safety and tolerability of 0.005% estriol vaginal gel in hormone receptor-positive postmenopausal women with early stage breast cancer in treatment with NSAIs in the adjuvant setting and symptoms of vaginal atrophy. To assess the efficacy of 0.005% estriol vaginal gel in the treatment of symptoms and signs of vaginal atrophy in hormone receptorpositive postmenopausal women with early stage breast cancer in treatment with NSAIs and symptoms of vaginal atrophy. To measure the impact of treatment with 0.005% estriol vaginal gel in sexual function of hormone receptor-positive postmenopausal women with early stage breast cancer in treatment with NSAIs and symptoms of vaginal atrophy Evaluar los niveles de estriol, estradiol, estrona, FSH y LH tras el tratamiento de los síntomas de la atrofia vaginal con el gel vaginal de estriol 0,005% en mujeres postmenopáusicas con cáncer de mama en estadio precoz y receptores hormonales positivos en tratamiento adyuvante con inhibidores de aromatasa Evaluar la seguridad y tolerabilidad del gel vaginal de estriol 0,005% Evaluar la eficacia del gel vaginal de estriol 0,005% en el tratamiento de los síntomas y signos de la atrofia vaginal Medir el impacto del tratamiento con el gel vaginal de estriol 0,005% en la función sexual

E.2.3

Trial contains a sub-study

E.3

Principal inclusion criteria

No 1. Written informed consent prior to beginning specific protocol procedures. 2. Patients must have histological confirmation of breast adenocarcinoma with stage I-IIIA, documented at a local pathology department. 3. The breast tumors must be estrogen-receptor positive and/or progesterone receptor positive (?1% of stained tumor cells by IHC as determined by the local laboratory) with any HER2 status. 4. Postmenopausal status defined as: 12 months of spontaneous amenorrhea or 6 months of spontaneous amenorrhea with serum FSH levels > 40 mIU/ml or 6 weeks postsurgical bilateral oophorectomy with or without hysterectomy. 5. Patient must be receiving the non-steroidal aromatase inhibitors anastrozole or letrozole as breast cancer treatment in the adjuvant setting for a minimum of 6 months. 6. Women suffering from moderate to severe vaginal dryness according to the FDA guidelines for drug development in postmenopausal women (Center for Drug Evaluation and Research, CDER Jan 2003). A moderate symptom will be considered if the symptom is present, bothersome and annoying, and a severe symptom will be considered if the symptom is present, bothersome and annoying, and interferes with the normal patient activity. 7. Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1. 8. Adequate bone marrow as defined by the following laboratory values: a. Absolute Neutrophil Count (ANC) ? 1.5 x 109/L. b. Platelets (plt) ? 100 x 109/L. c. Hemoglobin (Hgb) ? 10 g/dl. 9. Patient has adequate organ function as defined by the following laboratory values: d. Serum creatinine ? 1.5 x ULN. e. Bilirubin ? 1.5 × ULN. f. Alkaline phosphatase ? 2 × ULN. g. AST and ALT ? 2 × ULN. 10. Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests and other study procedures. consentimiento informado por escrito antes de iniciar procedimientos específicos del protocolo. 2. Los pacientes deben tener confirmación histológica de adenocarcinoma de mama en estadio I-IIIA, documentado en un departamento de patología local. 3. Los tumores de mama deben ser receptores de estrógenos positivos y / o receptor de progesterona positivo (?1% de las células tumorales teñidas por IHC según lo determinado por el laboratorio local) con cualquier estado de HER2. 4. Estado posmenopáusica defininido como: 12 meses de amenorrea espontánea o 6 meses de amenorrea espontánea con niveles séricos de FSH> 40 mUI / ml o 6 semanas ooforectomía bilateral postquirúrgica con o sin histerectomía. 5. La paciente debe estar recibiendo inhibidores de aromatasa no esteroideos anastrozol o letrozol como tratamiento para el cáncer de mama en el tratamiento adyuvante durante un mínimo de 6 meses. 6. Mujeres que sufren de sequedad vaginal moderada a severa según las directrices de la FDA para el desarrollo de fármacos en mujeres posmenopáusicas. Un síntoma es moderado si está presente y es molesto, y un síntoma grave será si está presente, es molesto, e interfiere con la actividad normal de la paciente. 7. Estado functional de 0 ó 1 según el Eastern Cooperative Oncology Group (PS ECOG). 8. Médula ósea en buen estado definido por los siguientes valores de laboratorio: a. Recuento absoluto de neutrófilos (RAN) ? 1,5 x 109 / L. b. Plaquetas (PLT) ? 100 x 109 / L. c. Hemoglobina (Hgb) ? 10 g / dl. 9 Órganos en buen estado definido los siguientes valores de laboratorio: d. Creatinina sérica ? 1,5 x LSN. e. Bilirrubina ? 1,5 × LSN. f. Fosfatasa alcalina ? 2 × LSN. g. AST y ALT ? 2 × LSN. 10. Disposición y capacidad para cumplir con las visitas programadas, el plan de tratamiento, pruebas de laboratorio y otros procedimientos del estudio.

E.4

Principal exclusion criteria

1. Stage IIIB-IV breast cancer or bilateral breast cancer. 2. Treatment with any other current anti-tumoral therapy (chemotherapy, anti-Her2?etc) besides the NSAI. Pamidronate or Alendronate are permitted. 3. Prior history of other malignancy within 5 years of study entry, aside from non-melanoma skin cancer or carcinoma-in-situ of the uterine cervix adequately treated. 4. Postmenopausal uterine bleeding. Vaginal bleeding of unknown etiology. 5. Patients with endometrial thickness equal to or greater than 4 mm measured by transvaginal ultrasound. 6. Patients who have received any type of vulvovaginal treatment in the 15 days prior to the start of the study. 7. Use of any hormone, natural (phytoestrogens) or herbal products for the treatment of menopausal symptoms within the last 6 months. 8. Current or previous history of thromboembolic disease or coagulopathies. 9. Severe cardiovascular or respiratory diseases in the previous 6 months. 10. Renal Impairment. 11. Hepatitis B and/or hepatitis C carriers (unless with normal hepatic function). 12. Known human immunodeficiency virus infection. 13. Known hypersensitivity to NSAI. 14. Other severe acute or chronic medical or psychiatric condition, or laboratory abnormality that would impart, in the judgment of the investigator, excess risk associated with study participation or study drug administration, or which, in the judgment of the investigator, would make the patient inappropriate for entry into this study. 15. Previous investigational treatment for any condition or participation in any clinical trial within 4 weeks of inclusion date. Cáncer de mama estadio IIIB-IV o cáncer de mama bilateral. 2. Tratamiento con cualquier otra terapia anti-tumoral (quimioterapia, anti-Her2 ... etc) además de la IANS. Se permiten pamidronato o alendronato. 3. Antecedentes de otra enfermedad maligna en los 5 años previos al estudio, aparte de cáncer de piel no melanoma o carcinoma in situ del cuello uterino tratado adecuadamente. 4. Sangrado uterino posmenopáusico. Sangrado vaginal de etiología desconocida. 5. Pacientes con grosor endometrial igual o mayor a 4 mm medido por ecografía transvaginal. 6. Pacientes que hayan recibido algún tipo de tratamiento vulvovaginal en los 15 días anteriores al inicio del estudio. 7. Uso de cualquier hormona, natural (fitoestrógenos) o productos a base de hierbas para el tratamiento de los síntomas de la menopausia en los últimos 6 meses. 8. Historia actual o previa de enfermedad tromboembólica o coagulopatías. 9. Enfermedades cardiovasculares o respiratorias severas en los últimos 6 meses. 10. Insuficiencia renal. 11. Hepatitis B y / o portadores de hepatitis C (a no ser que tengan función hepática normal). 12. Infección por VIH. 13. Hipersensibilidad conocida a IANS. 14. Otra anomalía médica, aguda o crónica, grave o enfermedad psiquiátrica, o alteración de laboratorio que podría considerar, a juicio del investigador, un riesgo asociado la participación en el estudio o la administración de fármacos del estudio, o que, a juicio del investigador, considere la participación en estudio inapropiada para la paciente. 15. Tratamiento con fármaco en investigación para cualquier indicación o participación en un ensayo clínico dentro de las 4 semanas previas a la fecha de inclusión.

E.5 End points E.5.1

Primary end point(s)

Variation in serum levels of FSH from baseline to 12 weeks of treatment. Variación de los niveles séricos de FSH de Basal a 12 semanas de tratamiento.

E.5.1.1

Timepoint(s) of evaluation of this end point

12 weeks of treatment 12 semanas de tratamiento

E.5.2

Secondary end point(s)

Variation in serum levels of FSH at different time points compared to baseline (weeks 1, 3 and 8). Variation in serum levels of LH and plasma levels of estriol, estradiol and estrone, at different time points compared to baseline (weeks 1, 3, 8 and 12). AEs according to the Medical Dictionary for Regulatory Activities (MedDRA) Changes in vaginal dryness and other symptoms and signs of vaginal atrophy; changes in vaginal maturation value and changes in vaginal pH at week 3 and week 12 vs baseline. Changes in sexual function measured by the Female Sexual Function Index (FSFI ) scale at week 3 and week 12 vs baseline. Variación en los niveles séricos de FSH en diferentes tiempos (semana 1, 3 y 8) en comparación con la basal. Variación en los niveles séricos de LH y de plasma de estriol, estradiol y estrona, en diferentes tiempos (semana 1, 3, 8 y 12) en comparación con la basal. Acontecimientos Adversos de acuerdo con el Diccionario Médico para las actividades de regulación (MedDRA) Cambios en la sequedad vaginal y otros síntomas y signos de atrofia vaginal; cambios en el valor de maduración vaginal y los cambios en el pH vaginal en la semana 3 y la semana 12 vs basal. Los cambios en la función sexual medidos por el Índice de Función Sexual (FSFI) en la semana 3 y la semana 12 vs basal.

E.5.2.1

Timepoint(s) of evaluation of this end point

Weeks 1, 3, 8, 12 of treatment Semanas 1, 3, 8 y 12 de tratamiento

E.6 and E.7 Scope of the trial E.6

Scope of the trial

E.6.1

Diagnosis

No

E.6.2

Prophylaxis

No

E.6.3

Therapy

Yes

E.6.4

Safety

Yes

E.6.5

Efficacy

Yes

E.6.6

Pharmacokinetic

No

E.6.7

Pharmacodynamic

No

E.6.8

Bioequivalence

No

E.6.9

Dose response

No

E.6.10

Pharmacogenetic

No

E.6.11

Pharmacogenomic

No

E.6.12

Pharmacoeconomic

No

E.6.13

Others

No

E.7

Trial type and phase

E.7.1

Human pharmacology (Phase I)

No

E.7.1.1

First administration to humans

No

E.7.1.2

Bioequivalence study

No

E.7.1.3

Other

No

E.7.1.3.1 Other trial type description E.7.2

Therapeutic exploratory (Phase II)

Yes

E.7.3

Therapeutic confirmatory (Phase III)

No

E.7.4

Therapeutic use (Phase IV)

No

E.8 Design of the trial E.8.1

Controlled

Yes

E.8.1.1

Randomised

Yes

E.8.1.2

Open

No

E.8.1.3

Single blind

No

E.8.1.4

Double blind

Yes

E.8.1.5

Parallel group

Yes

E.8.1.6

Cross over

No

E.8.1.7

Other

No

E.8.2

Comparator of controlled trial

E.8.2.1

Other medicinal product(s)

No

E.8.2.2

Placebo

Yes

E.8.2.3

Other

No

E.8.2.4

Number of treatment arms in the trial

2

E.8.3

The trial involves single site in the Member State concerned No

E.8.4

The trial involves multiple sites in the Member State concerned

Yes

E.8.4.1

Number of sites anticipated in Member State concerned

4

E.8.5

The trial involves multiple Member States

Yes

E.8.5.1

Number of sites anticipated in the EEA

5

E.8.6 Trial involving sites outside the EEA E.8.6.1

Trial being conducted both within and outside the EEA

No

E.8.6.2

Trial being conducted completely outside of the EEA

No

E.8.7

Trial has a data monitoring committee

Yes

E.8.8

Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial

LVLS Ultima visita de la última paciente

E.8.9 Initial estimate of the duration of the trial E.8.9.1

In the Member State concerned years

E.8.9.1

In the Member State concerned months

E.8.9.1

In the Member State concerned days

E.8.9.2

In all countries concerned by the trial months

11

11

F. Population of Trial Subjects F.1 Age Range F.1.1

Trial has subjects under 18

No

F.1.1.1

In Utero

No

F.1.1.2

Preterm newborn infants (up to gestational age < 37 weeks) No

F.1.1.3

Newborns (0-27 days)

No

F.1.1.4

Infants and toddlers (28 days-23 months)

No

F.1.1.5

Children (2-11years)

No

F.1.1.6

Adolescents (12-17 years)

No

F.1.2

Adults (18-64 years)

Yes

F.1.2.1

Number of subjects for this age range:

50

F.1.3

Elderly (>=65 years)

Yes

F.1.3.1

Number of subjects for this age range:

20

F.2 Gender F.2.1

Female

Yes

F.2.2

Male

No

F.3 Group of trial subjects F.3.1

Healthy volunteers

No

F.3.2

Patients

Yes

F.3.3

Specific vulnerable populations

No

F.3.3.1

Women of childbearing potential not using contraception

No

F.3.3.2

Women of child-bearing potential using contraception

No

F.3.3.3

Pregnant women

No

F.3.3.4

Nursing women

No

F.3.3.5

Emergency situation

No

F.3.3.6

Subjects incapable of giving consent personally

No

F.3.3.7

Others

No

F.4 Planned number of subjects to be included F.4.1

In the member state

50

F.4.2

For a multinational trial

F.4.2.1

In the EEA

70

F.4.2.2

In the whole clinical trial

70

F.5

Plans for treatment or care after the subject has ended the participation in the trial (if it is different from the expected normal treatment of that condition)

None Ninguno

G. Investigator Networks to be involved in the Trial G.4 Investigator Network to be involved in the Trial: 1 G.4.1

Name of Organisation

GEICAM Spanish Breast Cancer Group

G.4.3.4

Network Country

Spain

N. Review by the Competent Authority or Ethics Committee in the country concerned N.

Competent Authority Decision

Authorised

N.

Date of Competent Authority Decision

2015-02-26

N.

Ethics Committee Opinion of the trial application

Favourable

N.

Ethics Committee Opinion: Reason(s) for unfavourable opinion

N.

Date of Ethics Committee Opinion

2015-02-05

P. End of Trial P.

End of Trial Status

Completed

EU Clinical Trials Register Service Desk: https://servicedesk.ema.europa.eu European Medicines Agency © 1995-2018 | 30 Churchill Place, Canary Wharf, London E14 5EU

Smile Life

When life gives you a hundred reasons to cry, show life that you have a thousand reasons to smile

Get in touch

© Copyright 2015 - 2024 PDFFOX.COM - All rights reserved.