Zobrazeno 1 - 10
of 35
pro vyhledávání: '"C Brun—Strang"'
Autor:
Jacques Massol, Alain Puech, Jean-Pierre Boissel, A. Alperovitch, M. Bamberger, B. Bégaud, O. Blin, P. Blin, G. Bréart, C. Brun Strang, M. Buyse, A. Castot, M. Chauvenet, A. Chicoye, N. David, F. De Bels, R. De Sahb Berkovitch, E. Dohin, F. Fagnani, B. Falissard, C. Gastaldi-Menager, I. Giri, M. Haim, J.M. Joubert, M. Lapeyre-Mestre, C. Lassale, I. Marchant Ramirez, F. Meyer, J. Micallef, M. Mollimard, T. Moreau-Defarges, L. Pazart, L. Perret, M. Pigeon, C. Rumeau Pichon, Ph. Tcheng, M. Woler, L. Zanetti, M. Zylberman
Publikováno v:
Therapies. 62:417-425
Resume L’interet de sante publique des medicaments (ISP) est un critere d’evaluation recent (decret d’octobre 1999) et specifiquement francais qui, faute d’elements disponibles au moment de son appreciation, reste a ce jour souvent incomplete
Autor:
Muriel Vray, Bernard Hamelin, Patrice Jaillon, M. Andréjak, R. Benamouzig, J.-P. Boissel, C. Bremard-Oury, C. Brun-Strang, E. Caulin, D. Cellier, D. Costagliola, V. Daurat, A. El Hasnaoui, J.-M. Goehrs, B. Hamelin, P. Jaillon, C. Jouan-Flahault, J.-L. Montastruc, N. Moore, A. Puech, M. Ricatte, P. Ricordeau, M.-H. Rodde-Dunet, E. Rouffiac, T. Simon, P. Simon, A. Spriet, E. Van Ganse, P. Velicitat, M. Vray
Publikováno v:
Therapies. 60:345-349
The respective roles of controlled clinical trials and observational studies (cohort or case-control studies) in evaluating the efficacy, safety and usefulness of a drug were analysed. A randomised, controlled, double-blind study is the best method o
Autor:
P. Jaillon, E. Caulin, M. Vray, E. Van Ganse, Alain J. Puech, E. Rouffiac, Jean-Pierre Boissel, Jean-Marie Goehrs, M. Ricatte, D. Cellier, C. Brun-Strang, P. Simon, Patrice Jaillon, A. Spriet, Chrystel Jouan-Flahault, M.-H. Rodde-Dunet, Michel Andrejak, Bernard Hamelin, B. Hamelin, Muriel Vray, Tabassome Simon, J. L. Montastruc, Dominique Costagliola, A El Hasnaoui, P. Ricordeau, C. Bremard-Oury, P. Velicitat, Robert Benamouzig, V. Daurat, Nicholas Moore
Publikováno v:
Therapies. 60:339-344
Resume La place relative des essais cliniques comparatifs et des etudes observationnelles (cohortes ou etudes castemoins) a ete etudiee dans l’objectif d’evaluer l’efficacite, la tolerance et l’interet de sante publique d’un medicament. L
Autor:
Yvon Lebranchu, G Priol, C Le Pen, H Lilliu, A. Al Najjar, O Reigneau, Mathias Büchler, C Brun-Strang
Publikováno v:
Clinical Transplantation. 18:247-253
Purpose: Based on the data of clinical trial CHI-F-02 comparing the efficacy and safety of basiliximab (Simulect®) vs. anti-thymocyte globulin (Thymoglobulin®) in renal transplant induction, we carried out an economic evaluation. Method: This pharm
Autor:
Marie Fouchard, Faiez Zannad, E. Autret-Leca, J.-P. Bader, M. Bellet, J.-F. Bergmann, M. Bernard-Harlaud, C. Bernaud, R. Bordet, G. Bouvenot, C. Brun-Strang, A. Castaigne, N. Dumarcet, E. Eschwège, M. Gallard, I. Giri, B. Hamelin, A. Jeanblanc, P. Jolliet, H. Kolsky, D. Lagarde, G. Lapeyre, C. Lassale, J.-P. Lehner, H. Lelouët, M. Malbezin, S. Paulmier-Bigot, M. Pigeon, S. Ravoire, P. Ricordeau, B. Rouveix, J. Soletti, S. Tardieu, J.-L. Thomas, C. Thuillez
Publikováno v:
Therapies. 59:323-328
The round table elected to focus its discussion on trials that, in terms of their importance, are likely to modify medical practices and behaviour. Such trials may be pre- or postmarketing studies. For the findings of a trial to result in a change in
Autor:
Marie Fouchard, Faiez Zannad, E. Autret-Leca, J.-P. Bader, M. Bellet, J.-F. Bergmann, M. Bernard-Harlaud, C. Bernaud, R. Bordet, G. Bouvenot, C. Brun-Strang, A. Castaigne, N. Dumarcet, E. Eschwège, M. Gallard, I. Giri, B. Hamelin, A. Jeanblanc, P. Jolliet, H. Kolsky, D. Lagarde, G. Lapeyre, C. Lassale, J.-P. Lehner, H. Lelouët, M. Malbezin, S. Paulmier-Bigot, M. Pigeon, S. Ravoire, P. Ricordeau, B. Rouveix, J. Soletti, S. Tardieu, J.-L. Thomas, C. Thuillez
Publikováno v:
Therapies. 59:317-322
Resume La table ronde a choisi d’orienter sa discussion sur les essais qui, par leur importance, sont susceptibles de modifier les pratiques medicales et les comportements. Ces essais peuvent etre pre- ou post-AMM (autorisation de mise sur le march
Autor:
Jacques Massol, Alain Puech, Jean-Pierre Boissel, A. Alperovitch, M. Bamberger, B. Begaud, O. Blin, P. Blin, G. Breart, C. Brun Strang, M. Buyse, A. Castot, M. Chauvenet, A. Chicoye, N. David, F. De Bels, R. De Sahb Berkovitch, E. Dohin, F. Fagnani, B. Falissard, C. Gastaldi-Menager, I. Giri, M. Haim, J.M. Joubert, M. Lapeyre-Mestre, C. Lassale, I. Marchant Ramirez, F. Meyer, J. Micallef, M. Mollimard, T. Moreau-Defarges, L. Pazart, L. Perret, M. Pigeon, C. Rumeau Pichon, Ph. Tcheng, M. Woler, L. Zanetti, M. Zylberman
Publikováno v:
Therapie. 62(5)
The Public Health Benefit (PHB) of new medicines is a recent and French-specific criterion (October 1999 decree) which is often only partially documented in the transparency files due to a lack of timely information. At the time of the first reimburs
Publikováno v:
Value in Health. 5(6)
Autor:
C Brun—Strang, M Ziegler
Publikováno v:
Value in Health. 6:769-770
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