Using epidemiological registry data to provide background rates as context for adverse events in a rheumatoid arthritis drug development program: a coordinated approach.

Fredrik Nyberg, Johan Askling, Niklas Berglind, Stefan Franzén, Meilien Ho, Marie Holmqvist, Laura Horne, Kathy Lampl, Kaleb Michaud, Dimitrios A Pappas, George Reed, Deborah Symmons, Eiichi Tanaka, Trung N Tran, Suzanne Verstappen, Eveline Wesby-van Swaay, Hisashi Yamanaka, Jeffrey D Greenberg

Research output: Contribution to journal › Article › peer-review

1 results

Finished
Arthritis Research UK Centre of Excellence in Epidemiology.
Symmons, D. (PI), Bruce, I. (CoI), Dixon, W. (CoI), Felson, D. (CoI), Hyrich, K. (CoI), Lunt, M. (CoI), Mcbeth, J. (CoI), O'Neill, T. (CoI) & Verstappen, S. (CoI)
1/08/13 → 31/07/18
Project: Research

Using epidemiological registry data to provide background rates as context for adverse events in a rheumatoid arthritis drug development program: a coordinated approach.

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Arthritis Research UK Centre of Excellence in Epidemiology.