Literature DB >> 27335134

Letting post-marketing bridge the evidence gap: the case of orphan drugs.

Roberta Joppi1, Chiara Gerardi2, Vittorio Bertele'2, Silvio Garattini2.   

Abstract

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Year:  2016        PMID: 27335134     DOI: 10.1136/bmj.i2978

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


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  8 in total

Review 1.  [Orphan drugs from the perspective of the Drug Commission of the German Medical Association : Opportunities and challenges].

Authors:  Wolf-Dieter Ludwig
Journal:  Internist (Berl)       Date:  2019-04       Impact factor: 0.743

Review 2.  Benefits, benefits, once more benefits... with no risk? Stop overlooking the harms of medicines.

Authors:  Silvio Garattini; Vittorio Bertele'
Journal:  Eur J Clin Pharmacol       Date:  2017-11-27       Impact factor: 2.953

3.  Payers' Views of the Changes Arising through the Possible Adoption of Adaptive Pathways.

Authors:  Michael Ermisch; Anna Bucsics; Patricia Vella Bonanno; Francis Arickx; Alexander Bybau; Tomasz Bochenek; Marc van de Casteele; Eduardo Diogene; Jurij Fürst; Kristina Garuolienė; Martin van der Graaff; Jolanta Gulbinovič; Alan Haycox; Jan Jones; Roberta Joppi; Ott Laius; Irene Langner; Antony P Martin; Vanda Markovic-Pekovic; Laura McCullagh; Einar Magnusson; Ellen Nilsen; Gisbert Selke; Catherine Sermet; Steven Simoens; Robert Sauermann; Ad Schuurman; Ricardo Ramos; Vera Vlahovic-Palcevski; Corinne Zara; Brian Godman
Journal:  Front Pharmacol       Date:  2016-09-28       Impact factor: 5.810

Review 4.  Adaptive Pathways: Possible Next Steps for Payers in Preparation for Their Potential Implementation.

Authors:  Patricia Vella Bonanno; Michael Ermisch; Brian Godman; Antony P Martin; Jesper Van Den Bergh; Liudmila Bezmelnitsyna; Anna Bucsics; Francis Arickx; Alexander Bybau; Tomasz Bochenek; Marc van de Casteele; Eduardo Diogene; Irene Eriksson; Jurij Fürst; Mohamed Gad; Ieva Greičiūtė-Kuprijanov; Martin van der Graaff; Jolanta Gulbinovic; Jan Jones; Roberta Joppi; Marija Kalaba; Ott Laius; Irene Langner; Ileana Mardare; Vanda Markovic-Pekovic; Einar Magnusson; Oyvind Melien; Dmitry O Meshkov; Guenka I Petrova; Gisbert Selke; Catherine Sermet; Steven Simoens; Ad Schuurman; Ricardo Ramos; Jorge Rodrigues; Corinne Zara; Eva Zebedin-Brandl; Alan Haycox
Journal:  Front Pharmacol       Date:  2017-08-23       Impact factor: 5.810

Review 5.  A systematic literature review of evidence-based clinical practice for rare diseases: what are the perceived and real barriers for improving the evidence and how can they be overcome?

Authors:  Ana Rath; Valérie Salamon; Sandra Peixoto; Virginie Hivert; Martine Laville; Berenice Segrestin; Edmund A M Neugebauer; Michaela Eikermann; Vittorio Bertele; Silvio Garattini; Jørn Wetterslev; Rita Banzi; Janus C Jakobsen; Snezana Djurisic; Christine Kubiak; Jacques Demotes-Mainard; Christian Gluud
Journal:  Trials       Date:  2017-11-22       Impact factor: 2.279

Review 6.  Current landscape of clinical development and approval of advanced therapies.

Authors:  Carolina Iglesias-Lopez; Antonia Agustí; Antoni Vallano; Merce Obach
Journal:  Mol Ther Methods Clin Dev       Date:  2021-11-11       Impact factor: 6.698

Review 7.  Methodological Characteristics of Clinical Trials Supporting the Marketing Authorisation of Advanced Therapies in the European Union.

Authors:  Carolina Iglesias-Lopez; Antònia Agustí; Antonio Vallano; Merce Obach
Journal:  Front Pharmacol       Date:  2021-11-29       Impact factor: 5.810

Review 8.  How Surrogate and Chemical Genetics in Model Organisms Can Suggest Therapies for Human Genetic Diseases.

Authors:  Katherine A Strynatka; Michelle C Gurrola-Gal; Jason N Berman; Christopher R McMaster
Journal:  Genetics       Date:  2018-03       Impact factor: 4.562

  8 in total

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