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Responders vs clinical response: a critical analysis of data from linaclotide phase 3 clinical trials in IBS-C
BACKGROUND: US Food and Drug Administration (FDA) set a rigorous standard for defining patient responders in irritable bowel syndrome-C (IBS-C; i.e., FDA's Responder Endpoint) for regulatory approval. However, this endpoint's utility for health-care practitioners to assess clinical respons...
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| Vydáno v: | Neurogastroenterol Motil |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BlackWell Publishing Ltd
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4282394/ https://ncbi.nlm.nih.gov/pubmed/24382134 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nmo.12264 |
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