Early dose optimization of golimumab induces late response and long-term clinical benefit in moderately to severely active ulcerative colitis

Author:

Taxonera Carlos1ORCID,Iborra Marisa2,Bosca-Watts Marta Maia3,Rubio Saioa4,Nantes Óscar4,Higuera Rebeca5,Bertoletti Federico6,Martínez-Montiel Pilar7,Sierra-Ausin Mónica8,Manceñido Noemí9,Lázaro Pérez-Calle José10,Algaba Alicia11,Olivares David1ORCID,Alba Cristina1

Affiliation:

1. Department of Gastroenterology, Inflammatory Bowel Disease Unit, Hospital Clínico San Carlos and Instituto de Investigación del Hospital Clínico San Carlos (IdISSC), Madrid, Spain;

2. Department of Gastroenterology and CIBERehd, Hospital Universitario La Fe, Valencia, Spain;

3. Department of Gastroenterology, Inflammatory Bowel Disease Unit, Hospital Clínico de Valencia, Valencia, Spain;

4. Department of Gastroenterology, Complejo Hospitalario de Navarra and Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain;

5. Department of Gastroenterology, Hospital Urduliz, Vizcaya, Spain;

6. Department of Gastroenterology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain;

7. Department of Gastroenterology, Hospital 12 de Octubre, Madrid, Spain;

8. Department of Gastroenterology, Hospital de León, León, Spain;

9. Department of Gastroenterology, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain;

10. Department of Gastroenterology, Hospital Universitario Fundación Alcorcón, Madrid, Spain;

11. Department of Gastroenterology, Hospital Universitario de Fuenlabrada, Madrid, Spain

Publisher

Informa UK Limited

Subject

General Medicine

Reference28 articles.

1. Subcutaneous Golimumab Induces Clinical Response and Remission in Patients With Moderate-to-Severe Ulcerative Colitis

2. Subcutaneous Golimumab Maintains Clinical Response in Patients With Moderate-to-Severe Ulcerative Colitis

3. US Food and Drug Administration. Simponi Summary of Product Characteristics [Internet] [cited 2018 May 27]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/125289s024lbl.pdf

4. European Medicines Agency. Simponi Summary of Product Characteristics [Internet] [cited 2018 Nov 6]. Available from: https://ec.europa.eu/health/documents/community-register/2018/20180702141555/anx_141555_en.pdf

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